exam 3 Flashcards

1
Q

Biochemical tests include all of the following except_________.
A) presence of catalase
B) presence of oxidase
C) colony morphology
D) sugar fermentation
E) gas production

A

Colony morphology

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2
Q

Which sample does not require sterile needle aspiration?
A. Feces
B. CSF (cerebrospinalfluid)
C. Blood

A

Feces

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3
Q

What type of test will detect minute amount of soluble antigens?
A. Precipitation
B. Agglutination
C. Specificity
D. sensitivity

A

Precipitation

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4
Q

Which of the following is not one of the main categories for identifying microbes?
A) Radiologic
B) Phenotypic
C) Genotypic
D) Immunologic

A

Radiologic

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5
Q

Which medium contains three sugar sources and allows to differentiate between Salmonella, Shigella, Ecoli and Pseudomonas?
A) Triple sugar Iron Agar
B) EMB
C) McConkey
D) MTM

A

Triple sugar iron agar

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6
Q

What is the purpose of selective media?
a) To inhibit the growth of specific organisms
b) To differentiate between bacteria based on growth and appearance
c) To enhance the growth of fastidious organisms
d) To identify antibiotic resistance

A

To inhibit the growth of specific organisms

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7
Q

What diagnostic technique is mismatched?
A) EIA(enzymelinkedimmunoassay)-detectingantibodies(orantigen)usingenzymatic
reaction as a reporter
B) IF(Immunofluorescence)-detectingantibodies(orantibodies)usingfluorescentdyeas
a reporter
C) PCR (polymerase chain reaction - Detecting specific pathogen DNA using nucleic acid
probes
D) Microscopy - observation of stained cells or colonies on the plate

A

PCR (polymerase chain reaction - Detecting specific pathogen DNA using nucleic acid
probes

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8
Q

Phenotypic methods of identifying microorganisms in a patient sample are characterized as those that_________.
A) directly examine the organism’s appearance or behavior, which includes its metabolic abilities, environmental preferences and drug susceptibilities
B) analyze the genetic makeup of the microorganism, which conclusively diagnoses the infection
C) make use of the patient’s antibodies to precipitate the microorganism out of solution, or agglutinate the antigens in the sample
D) make use of color-changing antibodies directed against the microbe that will become visible to the naked eye when bound

A

Directly examine the organism’s appearance or behavior, which includes its metabolic abilities, environmental preferences, and drug susceptibilities

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9
Q

What is the primary difference between general-purpose media and selective media? a) Selective media are used to differentiate between different bacterial types. b) General-purpose media promote the growth of all microorganisms. c) Selective media inhibit the growth of certain bacteria. d) General-purpose media are only used for fungal cultures.

A

General-purpose media promote the growth of all microorganisms.

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10
Q

Which type of media is most appropriate for culturing Escherichia coli from a urinary tract infection? a) Blood agar b) MacConkey agar c) Triple-sugar iron (TSI) agar d) Thayer-Martin agar

A

MacConkey agar

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11
Q

How does the use of differential media help in the identification of bacteria? a) It provides a nutrient source for all bacteria. b) It allows for the visualization of different metabolic reactions. c) It prevents the growth of harmful bacteria. d) It inhibits the growth of anaerobic bacteria.

A

It allows for the visualization of different metabolic reactions.

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12
Q

What challenge is associated with the isolation of anaerobic pathogens? a) They are difficult to culture in the presence of oxygen. b) They grow rapidly on selective media. c) They do not survive well in the human body. d) They are resistant to most antibiotics.

A

They are difficult to culture in the presence of oxygen.

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13
Q

What is the purpose of a serial dilution tube test in antimicrobial susceptibility testing? a) To determine the smallest amount of agent needed to inhibit microbial growth. b) To distinguish
between aerobic and anaerobic bacteria. c) To differentiate between pathogenic and non-pathogenic bacteria. d) To identify the source of a urinary tract infection.

A

To determine the smallest amount of agent needed to inhibit microbial growth.

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14
Q

Adaptive immunity involves the response of_________.
A) skin barriers
B) B and T lymphocytes
C) lysozyme
D) mucous membranes
E) interferon

A

B and T lymphocytes

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15
Q

What type of cells secretes cytokines and helps to activate other immune cells? A) T cells
B) B cells
C) Dendritic cells D) Mast cells

A

T cells

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16
Q
  1. Killed or inactivated vaccines are prepared by_________.
    removal of virulence genes from the microbe
    treatment with formalin, heat, or radiation
    passage of the pathogen through unnatural hosts or tissue culture long-term subculturing of the microbe
    Allofthechoicesarecorrect
A

Treatment with formalin, heat, or radiation

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17
Q

Which of the following contribute to the limitless diversity generated from a relatively fixed number of immunoglobulin genes?
A)Random heavy and light chain reassortment only
B)Hypermutation, random heavy and light chain reassortment, and somatic recombination C)Hypermutation only
D)Somatic recombination only

A

Hypermutation, random heavy and light chain reassortment, and somatic recombination

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18
Q

The selection of T cells in thymus results in formation of
A) T-cells that are able to recognize self but do not bind too hard to it
B) T cells that are able to recognize self and bind hard to it
C) T cells that are unable to recognize self and only bind foreign antibodies
D) T cells that are unable to recognize self and unable to bind foreign antibodies

A

T-cells that are able to recognize self but do not bind too hard to it

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19
Q

What type of immunity is associated with B cells? A. Intracellular immunity
B. Humoral immunity
C. Tolerance immunity
D. Adaptive immunity

A

Humoral immunity

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20
Q

What is the exact purpose of T cell positive selection in the thymus?
A. To eliminate T cells that bind strongly to self-antigens
B. To retain T cells that can recognize MHC and self-peptides, but don’t bind too strongly to them
C. To generate memory T cells
D. To eliminate T cells that can not recognize MHC and self peptides

A

To retain T cells that can recognize MHC and self-peptides, but don’t bind too strongly to them

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21
Q

Which of the following is an intrinsic factor that determines immunogenicity? A. Size and nature of the molecule
B. Route of antigen exposure
C. Antigen dose
D. Presence of antibodies

A

Size and nature of the molecule

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22
Q

What is the role of MHC molecules in antigen recognition by T cells? A. To produce antibodies that bind to antigens
B. To present antigens to T cell receptors
C. To enhance antibody-antigen interaction
D. To eliminate antigens through phagocytosis

A

To present antigens to T cell receptors

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23
Q

What does the process of clonal selection in B cells involve? A. B cells binding to MHC molecules
B. Production of multiple types of antibodies by a single B cell C. Proliferation of antigen-specific B cells after activation
D. Elimination of B cells that bind weakly to antigens

A

Proliferation of antigen-specific B cells after activation

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24
Q

Which of the following is a key characteristic of active immunity?
A) Immunity is conferred immediately
B) No exposure to antigen is required
C) It develops memory cells, leading to long-lasting immunity
D) It involves the transfer of pre-formed antibodies

A

It develops memory cells, leading to long-lasting immunity

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25
Q

Passive immunity differs from active immunity in that:
A) It is achieved through exposure to antigens
B) It involves the activation of the recipient’s immune system
C) It provides rapid immunity without forming immune memory
D) It is maintained through memory cells

A

It provides rapid immunity without forming immune memory

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26
Q

Which of the following is an example of natural passive immunity?
A) Recovery from a disease
B) Receiving a vaccination
C) Transfer of antibodies through breast milk
D) Administration of antiserum

A

Transfer of antibodies through breast milk

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27
Q

Artificial active immunity involves:
A) Injecting pre-formed antibodies into the individual
B) The development of immunity after receiving a vaccination
C) Passing antibodies from mother to fetus via the placenta
D) Transfer of immune cells from a donor

A

The development of immunity after receiving a vaccination

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28
Q

Which of the following is true regarding passive immunity?
A) It requires exposure to an antigen for activation
B) It is maintained through the stimulation of memory cells
C) It decays rapidly and cannot be maintained
D) It develops over weeks and involves a latent period

A

It decays rapidly and cannot be maintained

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29
Q

What examples below are NOT active immunity types?
A) Contractingarhinovirusandgettingsickwiththecommoncold B) GettingvaccinatedagainstCovid19
C) Getting the pre-made antiserum injections for a serious illness D) Getting vaccinated against influenza

A

Getting serum injection

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30
Q

Which of the following terms and definitions is mismatched?
A) Neutralization - Antibodies bind to bacterial toxins or viruses to prevent host cell damage
B) Opsonization - Antibodies coat foreign cells to enhance phagocytosis
C) Fab region - Stem of the antibody that binds phagocyte receptors
D) IgM - Produced during primary immune response

A

Fab region

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31
Q

Compare and contrast IgG and IgM antibodies. Which of the following statements is correct?
A) IgG is a pentamer, while IgM has two antigen-binding sites
B) Both IgG and IgM are produced in the secondary immune response
C) IgG has two antigen-binding sites, while IgM is a pentamer
D) Both IgG and IgM are primarily produced during the primary immune response

A

IgG has two antigen-binding sites, while IgM is a pentamer

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32
Q

Which of the following correctly describes B cell activation and antibody production?
A) B cells recognize free antigens and present them to activated T helper cells
B) Cytokines from T helper cells help B cells differentiate into plasma and memory cells
C) Plasma cells produce antibodies, while memory cells provide long-term protection
D) All of the above

A

All of the above

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33
Q

Which of the following correctly pairs antibody structure with its function?
A) Fab region - Binds to phagocyte receptors to enhance phagocytosis
B) Fc region - Contains the antigen-binding site for neutralization
C) Fab region - Contains the antigen-binding site for specificity
D) Fc region - Neutralizes bacterial toxins and viruses

A

Fab region - Contains the antigen-binding site for specificity

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34
Q

Which of the following steps in antibody-mediated immunity is mismatched?
A) Antigen presentation - B cells present antigens to T helper cells on MHC type II
B) Cytokine release - T helper cells release cytokines to activate B cells
C) Plasma cell production - Short-lived cells that generate memory for long-term protection
D) Neutralization - Antibodies bind to viral proteins to prevent host cell destruction

A

Plasma cell production - Short-lived cells that generate memory for long-term protection

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35
Q

Which of the following statements about the primary and secondary immune responses is incorrect?
A) Primary immune response includes a latent period where no antibodies are detected.
B) IgM is the predominant antibody produced during the primary immune response.
C) Secondary immune responses depend on T helper cells to initiate antibody production. D) IgG is the predominant antibody produced during the secondary immune response.

A

Secondary immune responses depend on T helper cells to initiate antibody production.

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36
Q

What is the most likely reason for the shorter response time during a secondary immune response compared to a primary response?
A) Rapid production of IgM by naïve B cells.
B) The activation of pre-existing memory B cells that quickly produce IgG.
C) Faster activation of T helper cells by antigen-presenting cells.
D) Increased proliferation of plasma cells during the secondary response.

A

The activation of pre-existing memory B cells that quickly produce IgG.

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37
Q

Which of the following correctly pairs the feature with the immune response phase? A) IgM production - Primary immune response.
B) No latent period - Primary immune response.
C) Memory cell formation - Secondary immune response.
D) IgG predominance - Primary immune response.

A

IgM production - Primary immune response.

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38
Q

Which of the following events is shared by both primary and secondary immune responses? A) IgM is the main antibody produced.
B) Memory B cells are activated.
C) Antigen presentation by antigen-presenting cells.
D) No need for T helper cell activation.

A

Antigen presentation by antigen-presenting cells.

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39
Q

Which of the following combinations best summarizes the difference between primary and secondary immune responses?
A) Primary response: short-lived plasma cells, IgM; Secondary response: long-lived memory cells, IgG.
B) Primary response: no antigen presentation, IgG; Secondary response: requires T helper cells, IgM.
C) Primary response: long latency period, IgG; Secondary response: rapid antibody production, IgM.
D) Primary response: memory cells predominate, IgM; Secondary response: T helper cells predominate, IgG.

A

Primary response: short-lived plasma cells, IgM; Secondary response: long-lived memory cells, IgG.

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40
Q

Which of the following statements about complementarity-determining regions (CDRs) is correct?
A) CDRs are identical in all antibodies.
B) CDRs are part of the constant region of antibodies.
C) CDRs are variable regions within the antigen-binding site of antibodies. D) CDRs interact exclusively with the light chain of the antibody.

A

CDRs are variable regions within the antigen-binding site of antibodies.

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41
Q

What is the primary mechanism responsible for generating antibody diversity? A) Allelic exclusion in B cells.
B) Random somatic recombination of immunoglobulin gene segments.
C) Inactivation of meiotic recombination in somatic cells.
D) Binding of multiple epitopes to the same antibody.

A

Random somatic recombination of immunoglobulin gene segments.

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42
Q

Which of the following best describes allelic exclusion in B cells?
A) Each B cell expresses multiple antibody types simultaneously.
B) Each B cell expresses only one heavy and one light chain combination. C) Each B cell excludes CDR regions to produce a functional antibody.
D) B cells combine several antibody types to recognize diverse antigens.

A

Each B cell expresses only one heavy and one light chain combination.

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43
Q

Which of the following features contribute to the diversity of antigen-binding sites in antibodies?
A) Somatic recombination of gene segments only.
B) Hypermutation and random heavy/light chain reassortment only.
C) Random heavy/light chain reassortment, somatic recombination, and hypermutation. D) Random heavy/light chain reassortment and somatic recombination, excluding hypermutation.

A

Random heavy/light chain reassortment, somatic recombination, and hypermutation.

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44
Q

Which of the following combinations is mismatched?
A) Epitope - Recognized by antibodies, typically 8-12 amino acids long.
B) Binding affinity - Strength of binding between an antibody and its epitope.
C) Hypermutation - Occurs at a lower rate in the variable region compared to other genome areas.
D) Active gene - Result of somatic recombination in B cells.

A

Hypermutation - Occurs at a lower rate in the variable region compared to other genome areas.

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45
Q

What determines the specificity of antigen-antibody reactions? A. The size of the antigen
B. The complexity of the immune response
C. Lymphocyte receptors interacting with individual pathogens D. Physical form of the antigen

A

Lymphocyte receptors interacting with individual pathogens

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46
Q

What type of receptors do T lymphocytes (T cells) express? A. Membrane-bound immunoglobulins
B. B cell receptors (BCRs)
C. T cell receptors (TCRs)
D. Antibodies

A

T cell receptors (TCRs)

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47
Q

What type of immunity is associated with B cell receptors (BCRs)? A. Intracellular immunity
B. Humoral immunity
C. Adaptive immunity
D. Cellular immunity

A

Humoral immunity

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48
Q

What happens to the lymphocytes most efficiently reacting with an antigen?
A. They die due to negative selection.
B. They proliferate to form a clone of identical cells.
C. They recognize MHC molecules.
D. They bind to self-antigens strongly.

A

They proliferate to form a clone of identical cells.

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49
Q

Which property of adaptive immunity allows for a stronger and faster response upon subsequent antigen exposure?
A. Immunogenicity
B. Specificity
C. Tolerance D. Memory

A

Memory

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50
Q

What is the difference between a primary and secondary immune response?
A. Primary response involves memory cells, while secondary response does not.
B. Primary response occurs faster than secondary response.
C. Primary response activates lymphocytes, while secondary response is faster and stronger. D. Primary response occurs only in T cells, while secondary response involves B cells.

A

Primary response activates lymphocytes, while secondary response is faster and stronger.

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51
Q

What does vaccination achieve?
A. Activates autoimmunity
B. Induces tolerance to foreign pathogens
C. Confers immunity by exposing the immune system to weakened or killed pathogens D. Enhances the primary immune response

A

Confers immunity by exposing the immune system to weakened or killed pathogens

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52
Q

What is tolerance in the immune system?
A. The ability to attack self-antigens
B. The acquired inability to react to one’s own antigens
C. The capacity to bind to MHC molecules strongly D. The proliferation of B and T cells

A

The acquired inability to react to one’s own antigens

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53
Q

Which type of MHC is found on all nucleated cells? A. MHC Type II
B. MHC Type I
C. MHC Complex III
D. Both MHC Type I and Type II Answer:

A

MHC Type I

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54
Q

What happens if tolerance fails in the immune system? A. Clonal deletion occurs
B. Autoimmunity develops
C. T cells fail to recognize foreign antigens
D. Immunogens fail to induce a response

A

Autoimmunity develops

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55
Q

Where do precursor T cells mature and undergo selection? A. Bone marrow
B. Thymus
C. Spleen
D. Lymph nodes

A

Thymus

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56
Q

What is the purpose of negative selection during T cell development? A. To ensure T cells recognize self-antigens strongly
B. To eliminate T cells that bind too strongly to self-antigens
C. To proliferate T cells that fail to recognize MHC molecules D. To retain all T cells entering the thymus

A

To eliminate T cells that bind too strongly to self-antigens

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57
Q

What determines whether an antigen is an immunogen? A. The antigen’s ability to bind to TCRs
B. The antigen’s intrinsic and extrinsic properties
C. Its ability to evade recognition by lymphocytes
D. Its capacity to generate autoimmunity

A

The antigen’s intrinsic and extrinsic properties

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58
Q

Why are haptens not immunogenic on their own? A. They are too complex.
B. They are small molecules and lack carriers.
C. They do not bind to MHC molecules.
D. They interact only with B cell receptors.

A

They are small molecules and lack carriers.

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59
Q

What is an epitope?
A. A molecule that triggers autoimmunity
B. The entire antigen recognized by antibodies
C. A specific portion of an antigen bound by antibodies or TCRs D. A carrier molecule for haptens

A

A specific portion of an antigen bound by antibodies or TCRs

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60
Q

What is required for antigens to be recognized by T cell receptors (TCRs)? A. Binding to free-floating antigens
B. Association with MHC molecules
C. Presence of haptens
D. Interaction with antibodies

A

Association with MHC molecules

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61
Q

How is active immunity achieved?
A. By injecting pre-formed antibodies
B. By receiving immune cells from a donor
C. By exposure to an antigen through infection or vaccination D. By receiving antibodies through the placenta

A

By exposure to an antigen through infection or vaccination

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62
Q

What is a characteristic of passive immunity? A. It develops memory cells.
B. It provides long-lasting immunity.
C. It does not activate the immune system.
D. It requires exposure to an antigen.

A

It does not activate the immune system.

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63
Q

What is the key difference between active and passive immunity?
A. Active immunity uses pre-formed antibodies, while passive immunity generates a specific immune response.
B. Active immunity involves immune system activation, while passive immunity does not.
C. Passive immunity requires exposure to an antigen, while active immunity does not. D. Passive immunity lasts longer than active immunity.

A

Active immunity involves immune system activation, while passive immunity does not.

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64
Q

Which type of immunity develops memory cells? A. Passive immunity
B. Active immunity
C. Both active and passive immunity
D. Neither active nor passive immunity Answer:

A

Active immunity

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65
Q

Which is an example of natural active immunity? A. Vaccination for rabies
B. Recovering from an infection
C. Passing antibodies through breast milk
D. Receiving an antiserum injection

A

Recovering from an infection

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66
Q

Which scenario represents artificial passive immunity? A. Receiving a vaccination shot
B. Developing antibodies after infection
C. Passing antibodies to a fetus through the placenta
D. Receiving pre-formed antibodies through an antiserum injection

A

Receiving pre-formed antibodies through an antiserum injection

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67
Q

What distinguishes artificial immunity from natural immunity?
A. Artificial immunity is achieved through medical intervention, while natural immunity occurs naturally.
B. Artificial immunity always involves memory cell formation, while natural immunity does not. C. Natural immunity is faster than artificial immunity.
D. Natural immunity is only passive.

A

Artificial immunity is achieved through medical intervention, while natural immunity occurs naturally.

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68
Q

Why does passive immunity decay rapidly?
A. It lacks immune system activation and memory cell formation. B. It requires repeated antigen exposure.
C. It depends on booster immunizations.
D. It relies on antigen-reactive T cells.

A

It lacks immune system activation and memory cell formation.

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69
Q

What is an example of natural passive immunity? A. Breastfeeding
B. Receiving a vaccine
C. Developing antibodies after an infection
D. Receiving a blood transfusion with antibodies

A

Breastfeeding

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70
Q

How quickly does passive immunity confer protection? A. Over weeks with a latent period
B. Immediately upon receiving antibodies
C. Over a few months after infection
D. After repeated exposure to antigens

A

Immediately upon receiving antibodies

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71
Q

How is natural active immunity maintained? A. Through repeated antibody injections
B. Via stimulation of memory cells C. By constant exposure to antigens D. It cannot be maintained

A

Via stimulation of memory cells

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72
Q

What is an example of artificial active immunity? A. Passing antibodies through breast milk
B. Recovering from a disease naturally
C. Receiving a vaccination shot
D. Receiving pre-formed antibodies

A

Receiving a vaccination shot

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73
Q

What occurs during natural passive immunity?
A. The immune system produces antibodies in response to infection.
B. Antibodies are transferred from mother to child through breastfeeding. C. Pre-formed antibodies are injected into the body.
D. The immune system activates memory cells.

A

Antibodies are transferred from mother to child through breastfeeding

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74
Q

What type of immunity is conferred by receiving a rabies antiserum injection? A. Natural active immunity
B. Natural passive immunity
C. Artificial active immunity
D. Artificial passive immunity

A

Artificial passive immunity

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75
Q

What is the main role of an antibody? A. Facilitate antigen internalization
B. Neutralize foreign substances
C. Trigger apoptosis
D. Bind antigens and facilitate their removal

A

Bind antigens and facilitate their removal

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76
Q

How many B cell receptors (BCRs) are found on each B cell? A. About 10,000
B. About 50,000
C. About 100,000
D. About 1,000,000

A

About 100,000

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77
Q

What is the sequence of events in humoral immunity?
A. B cells bind antigens → T cells activate B cells → B cells proliferate and differentiate B. Antibodies are produced → B cells bind antigens → T cells activate B cells
C. Cytokines are released → Memory cells form → B cells bind antigens
D. B cells bind antigens → Memory cells degrade → Antibodies are stored

A

B cells bind antigens → T cells activate B cells → B cells proliferate and differentiate

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78
Q

What function do helper T cells perform during B cell activation? A. Degrade antigens
B. Release cytokines
C. Stimulate B cell proliferation and differentiation
D. Both B and C

A

Both B and C

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79
Q

Which of the following processes are performed by antibodies? A. Neutralization of toxins
B. Opsonization of pathogens
C. Phagocytosis of pathogens
D. Both A and B

A

Both A and B

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80
Q

Which class of antibody is most abundant in the body and produced during secondary immune responses?
A. IgM
B. IgA
C. IgG D. IgE

A

IgG

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81
Q

What is unique about the structure of IgM?
A. It is a dimer with two subunits.
B. It is a pentamer made of five IgG-like subunits. C. It has a single antigen-binding site.
D. It is found only on the surface of B cells.

A

It is a pentamer made of five IgG-like subunits.

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82
Q

Which region of an antibody binds to antigens? A. Fc region
B. Fab region
C. Heavy chain
D. Light chain

A

Fab region

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83
Q

What is the role of the Fc region of an antibody?
A. Binds to antigens
B. Facilitates antigen degradation
C. Binds to receptors on phagocytes to promote opsonization D. Prevents host cell destruction

A

Binds to receptors on phagocytes to promote opsonization

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84
Q

Which of the following are true about IgG?
A. It has two antigen-binding sites.
B. It is the most numerous antibody in serum.
C. It is produced mostly during the secondary immune response. D. All of the above

A

All of the above

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85
Q

What defines the class of an antibody? A. The Fc region
B. The type of light chain
C. The heavy chain
D. The Fab region

A

The heavy chain

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86
Q

During which immune response is IgM produced? A. Secondary immune response
B. Primary immune response
C. Both primary and secondary immune responses D. Neither primary nor secondary immune response

A

Primary immune response

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87
Q

What are the components of an antibody molecule? A. Two heavy chains and one light chain
B. Two heavy chains and two light chains
C. Four heavy chains
D. One heavy chain and two light chains

A

Two heavy chains and two light chains

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88
Q

Which of the following is a function of the Fab region? A. Binding to antigen
B. Binding to Fc receptors on phagocytes
C. Stimulating B cell proliferation
D. Both A and C

A

Binding to antigen

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89
Q

What is the function of antibodies during neutralization?
A. Coating foreign cells to promote phagocytosis
B. Preventing destruction of host cells by binding to toxins or viruses C. Triggering apoptosis of infected cells
D. Binding to the Fc receptors of phagocytes

A

Preventing destruction of host cells by binding to toxins or viruses

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90
Q

What occurs during the latent period of a primary immune response? A. Plasma cells produce IgM antibodies.
B. Memory cells are activated.
C. Antibodies are not detected.
D. IgG antibodies rise in the blood.

A

Antibodies are not detected.

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91
Q

Which antibody is primarily produced during the primary immune response? A. IgA
B. IgG
C. IgE
D. IgM

A

IgM

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92
Q

What type of cells are generated during the primary immune response? A. Short-lived plasma cells
B. Memory T cells
C. Memory B cells
D. All of the above

A

All of the above

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93
Q

What distinguishes the secondary immune response from the primary immune response? A. It produces mostly IgM.
B. It has a latent period.
C. It is faster and produces mostly IgG.
D. It requires T helper cell help for memory cells.

A

It is faster and produces mostly IgG.

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94
Q

What happens to IgG levels in the absence of antigen? A. They remain constant.
B. They continue to rise.
C. They decrease over time.
D. They convert to IgM.

A

They decrease over time

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95
Q

What allows the secondary immune response to be faster? A. Memory cells do not require T helper cell help.
B. Plasma cells are longer-lived.
C. Antigens bind more easily to B cells.
D. IgM antibodies are already present.

A

Memory cells do not require T helper cell help.

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96
Q

Which of the following steps are involved in adaptive immune response? A. Antigen-independent lymphocyte development
B. Antigen presentation to T and B cells
C. Antigen challenge and response by T and B cells
D. All of the above

A

All of the above

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97
Q

What type of immunity do B cells provide during an adaptive immune response? A. T cell-mediated immunity
B. Antibody-mediated immunity
C. Innate immunity
D. Phagocytic immunity

A

Antibody-mediated immunity

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98
Q

During the secondary immune response, what is the primary antibody produced? A. IgA
B. IgG
C. IgE
D. IgM

A

IgG

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99
Q

Which cells respond first to a secondary antigen exposure? A. Naive B cells
B. Plasma cells from the primary response
C. Memory cells
D. Helper T cells

A

Memory cells

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100
Q

Which of the following occurs during antigen challenge? A. Antibodies bind to the antigen.
B. T and B cells are activated.
C. Cytokines are released.
D. All of the above

A

All of the above

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101
Q

What is measured during a primary immune response to monitor antibody levels? A. IgG concentration
B. Antibody titer
C. Antigen concentration
D. Cytokine levels

A

Antibody titer

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102
Q

What is the primary role of memory cells during a secondary immune response? A. Activate T helper cells.
B. Ramp up antibody production quickly.
C. Produce cytokines.
D. Convert IgG to IgM.

A

Ramp up antibody production quickly.

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103
Q

Why are plasma cells in the primary immune response short-lived? A. They are quickly replaced by memory cells.
B. They only produce IgM.
C. They respond only to antigen-specific signals.
D. They function only during the latent period.

A

They are quickly replaced by memory cells.

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104
Q

What type of immune response involves T cell-mediated immunity? A. Innate immunity
B. Adaptive immunity
C. Humoral immunity
D. Passive immunity

A

Adaptive immunity

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105
Q

What is the primary characteristic of variable (V) domains in antibodies? A. They are different in complementarity-determining regions (CDRs).
B. They are identical in all antibodies.
C. They interact with the constant region of the antibody. D. They form the antigen-binding site.

A

They are different in complementarity-determining regions (CDRs).

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106
Q

What is an epitope?
A. The constant region of an antibody.
B. A type of antibody.
C. The part of the antigen recognized by the immune system. D. A receptor on B cells.

A

The part of the antigen recognized by the immune system.

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107
Q

How long is a typical epitope? A. 2–4 amino acids.
B. 8–12 amino acids long.
C. 20–30 amino acids.
D. More than 50 amino acids.

A

8–12 amino acids long.

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108
Q

What determines the strength of an antibody’s binding to its epitope? A. Hypermutation.
B. Binding affinity.
C. Allelic exclusion.
D. Antibody titer.

A

Binding affinity.

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109
Q

What mechanism generates antibody diversity? A. Somatic recombination.
B. Meiotic recombination.
C. Transcription and translation.
D. Hypermutation.

A

Somatic recombination.

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110
Q

What is the “genes in pieces” hypothesis?
A. Genes are inherited intact without changes.
B. Antibody genes are assembled from several gene segments. C. Genes are transcribed as a single unit.
D. Only the light chain contributes to diversity.

A

Antibody genes are assembled from several gene segments.

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111
Q

What is allelic exclusion?
A. Each B cell expresses only one antibody type.
B. Each T cell expresses multiple antibody types.
C. Only heavy chains are excluded during recombination. D. It ensures all antibodies are identical in structure.

A

Each B cell expresses only one antibody type.

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112
Q

How are heavy and light chains combined during antibody generation? A. They are assembled from a single gene segment.
B. They are randomly reassorted.
C. They are formed in response to hypermutation.
D. They do not undergo any recombination.

A

They are randomly reassorted.

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113
Q

What contributes to joint diversity in antibodies? A. Mutations in the constant region.
B. Random recombination of gene segments.
C. Use of pre-made antibodies.
D. Antigen binding to the Fc region.

A

Random recombination of gene segments.

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114
Q

What process introduces small changes in variable regions at a higher rate? A. Transcription errors.
B. Hypermutation.
C. Genetic recombination.
D. Epitope interactions.

A

Hypermutation.

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115
Q

What does the antigen-binding site of an antibody accommodate?
A. Binding of an epitope with both heavy and light chain variable regions. B. Binding of T cells to plasma cells.
C. Recognition of the Fc region of the antibody.
D. Interaction with complement proteins.

A

Binding of an epitope with both heavy and light chain variable regions.

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116
Q

What is somatic recombination?
A. A process where immunoglobulin genes rearrange in lymphocytes. B. A type of meiotic recombination occurring in sexual cells.
C. A mutation in T cell receptors.
D. A type of antigen-binding mechanism.

A

A process where immunoglobulin genes rearrange in lymphocytes.

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117
Q

Why does hypermutation occur in antibody genes? A. To enhance diversity in the variable regions.
B. To increase binding affinity for antigens.
C. To replace heavy chains with light chains.
D. To remove unwanted epitopes.

A

To enhance diversity in the variable regions.

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118
Q

What role do complementarity-determining regions (CDRs) play? A. They form the antigen-binding site of an antibody.
B. They enhance Fc region binding.
C. They ensure allelic exclusion.
D. They bind T cell receptors.

A

They form the antigen-binding site of an antibody.

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119
Q

How does the immune system generate almost limitless antibody diversity? A. Through somatic recombination.
B. By combining heavy and light chains randomly.
C. Through hypermutation.
D. By preventing somatic recombination.

A

Through somatic recombination, random reassortment, and hypermutation.

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120
Q

What are MHC molecules also called in humans? A) Major histocompatibility molecules
B) Human leukocyte antigens
C) Cytotoxic T cell markers
D) B cell receptors

A

Human leukocyte antigens

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121
Q

What type of cells do MHC Class I molecules present antigens to?
A) CD4+ T cells
B) CD8+ T cells
C) B cells
D) Macrophages

A

CD8+ T cells

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122
Q

What types of proteins can antigens processed by APCs originate from? A) Bacterial proteins
B) Viral proteins or cancer proteins
C) Only bacterial proteins
D) None of the above

A

Viral proteins or cancer proteins

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123
Q

What occurs when MHC Class I self-antigens trigger a host vs graft disease? A) The graft is recognized as foreign and attacked by T cytotoxic cells
B) The host cells attack the graft causing tissue rejection
C) The graft’s T cells attack the host body
D) The host immune system becomes tolerant of the graft

A

The graft is recognized as foreign and attacked by T cytotoxic cells

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124
Q

What is the opposite of host vs graft disease? A) Transplant rejection
B) Graft vs host disease
C) Immune tolerance
D) MHC compatibility

A

Graft vs host disease

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125
Q

Where are MHC Class II molecules primarily found?
A) On all nucleated cells
B) On antigen presenting cells, such as macrophages and dendritic cells C) On cytotoxic T cells
D) On red blood cells

A

On antigen presenting cells, such as macrophages and dendritic cells

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126
Q

What is the role of MHC Class II molecules in immune responses? A) To present antigens to CD8+ T cells
B) To present internalized antigens to CD4+ T cells
C) To activate cytotoxic T cells D) To destroy infected cells

A

To present internalized antigens to CD4+ T cells

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127
Q

What does the activation of Helper T cells (CD4+) by MHC Class II molecules result in? A) Activation of cytotoxic T cells
B) Destruction of infected cells
C) Release of cytokines that help other immune cells
D) Suppression of the immune response

A

Release of cytokines that help other immune cells

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128
Q

What does polymorphism in MHC molecules mean?
A) MHC molecules are identical across all individuals
B) There are many different alleles for each of the MHC genes C) There is only one type of MHC allele in a population
D) MHC molecules cannot vary between individuals

A

There are many different alleles for each of the MHC genes

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129
Q

What does polygeny in MHC molecules refer to?
A) Multiple copies of the same MHC gene
B) The presence of many different alleles for each gene
C) Different MHC molecules being expressed by different cells
D) Multiple genes contributing to the MHC molecules expressed in an individual

A

Multiple genes contributing to the MHC molecules expressed in an individual

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130
Q

What is the result of the unique combination of MHC molecules in each person?
A) Each person has identical immune responses
B) The immune system can only recognize a small number of pathogens C) Every person has a unique set of MHC molecules
D) The immune system becomes tolerant of all pathogens

A

Every person has a unique set of MHC molecules

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131
Q

What is the significance of HLA in humans?
A) It is a generic name for MHC molecules
B) It refers to the unique set of MHC molecules in humans C) It is a gene responsible for MHC expression
D) It is a foreign antigen in the body

A

It refers to the unique set of MHC molecules in humans

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132
Q

What is the primary role of T Cell Receptors (TCRs)? A) To bind only to self-MHC molecules
B) To bind both self-MHC and foreign peptides
C) To activate macrophages directly
D) To produce antibodies in response to pathogens

A

To bind both self-MHC and foreign peptides

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133
Q

Which of the following is NOT a mechanism that generates diversity in T Cell Receptors? A) Somatic recombination
B) Random chain reassortment C) Coding for joint diversity
D) Exon shuffling

A

Exon shuffling

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134
Q

How are T Cell Receptors similar to B cell receptors?
A) Both generate diversity through genetic mechanisms
B) Both bind to antigens on the surface of pathogens
C) Both have a constant region encoded by the same gene segments D) Both produce cytokines to fight infection

A

Both generate diversity through genetic mechanisms

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135
Q

What do MHC proteins on a cell’s surface reflect? A) The type of pathogens inside the cell
B) The composition of the proteins inside the cell
C) The cell’s external environment
D) The DNA sequence of the cell

A

The composition of the proteins inside the cell

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136
Q

What type of foreign antigens do T cytotoxic cells recognize? A) Foreign antigens embedded in MHC Class II molecules
B) Foreign antigens embedded in MHC Class I molecules
C) Antigens on the surface of pathogens
D) None of the above

A

Foreign antigens embedded in MHC Class I molecules

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137
Q

Which T cell subset interacts with macrophages and B cells, recognizing foreign antigens bound to MHC Class II molecules?
A) T cytotoxic cells B) T helper 1 cells
C) T helper 2 cells
D) None of the above

A

T helper 2 cells

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138
Q

What is the role of T cytotoxic cells?
A) To activate B cells to produce antibodies
B) To directly kill infected cells displaying foreign antigens on MHC Class I C) To activate macrophages to kill intracellular bacteria
D) To regulate immune responses after infection

A

To directly kill infected cells displaying foreign antigens on MHC Class I

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139
Q

What is the function of perforin in T cytotoxic cells?
A) To stimulate the production of antibodies
B) To create pores in the target cell membrane, leading to cell death C) To neutralize bacterial toxins
D) To activate helper T cells

A

To create pores in the target cell membrane, leading to cell death

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140
Q

Which of the following is a function of the Th1 subset of T helper cells? A) Activates B cells to produce antibodies
B) Activates macrophages to kill intracellular bacteria
C) Regulates the immune response after infection D) None of the above

A

Activates macrophages to kill intracellular bacteria

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141
Q

What is the primary function of Th2 cells?
A) To activate macrophages for innate immunity
B) To help B cells differentiate into plasma cells and produce antibodies C) To directly kill infected cells
D) To secrete cytokines that inhibit immune responses

A

To help B cells differentiate into plasma cells and produce antibodies

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142
Q

What is the role of T regulatory cells in the immune response? A) To promote inflammation
B) To activate cytotoxic T cells
C) To curb the immune response after the pathogen is defeated D) To increase the production of antibodies

A

To curb the immune response after the pathogen is defeated

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143
Q

Which of the following cytokines is secreted by Th1 cells to activate macrophages? A) Gamma interferon
B) Interleukin-10
C) Interleukin-4
D) None of the above

A

Gamma interferon

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144
Q

What is hypersensitivity?
A) An appropriate immune response that causes no harm to the body B) An inappropriate immune response that results in host damage
C) An immune response to only bacterial infections
D) None of the above

A

An inappropriate immune response that results in host damage

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145
Q

Which of the following describes the two major types of hypersensitivity? A) Antibody-mediated and cell-mediated
B) IgE-mediated and IgG-mediated
C) Acute and chronic
D) None of the above

A

Antibody-mediated and cell-mediated

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146
Q

How are hypersensitivity diseases categorized?
A) According to the organ involved and duration of the disease
B) According to antigens and effector mechanisms that produce disease C) Based on the severity of the disease
D) All of the above

A

All of the above

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147
Q

Which of the following is characteristic of Type 1 hypersensitivity? A) Immediate response mediated by IgE and mast cell sensitization B) Takes hours to develop
C) Involves IgG interaction with cell surface antigens
D) None of the above

A

Immediate response mediated by IgE and mast cell sensitization

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148
Q

What is an example of Type 1 hypersensitivity? A) Reaction to penicillin
B) Hay fever and bee venom reaction
C) Systemic lupus erythematosus (SLE)
D) Tuberculin test

A

Hay fever and bee venom reaction

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149
Q

What is the key feature of Type 2 hypersensitivity? A) Immediate reaction mediated by IgE
B) Cytotoxic IgG interaction with cell surface antigens C) Immune complex formation involving IgG
D) All of the above

A

Immune complex formation involving IgG

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150
Q

Which type of hypersensitivity involves the formation of immune complexes? A) Type 1
B) Type 2
C) Type 3
D) None of the above

A

Type 3

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151
Q

What is an example of Type 3 hypersensitivity? A) Hay fever
B) Systemic lupus erythematosus (SLE)
C) Poison ivy
D) Tuberculin test

A

Systemic lupus erythematosus (SLE)

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152
Q

Which type of hypersensitivity is delayed and mediated by Th1 cells and macrophages? A) Type 1
B) Type 2
C) Type 3
D) Type 4

A

Type 4

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153
Q

What is an example of Type 4 hypersensitivity? A) Systemic lupus erythematosus (SLE)
B) Tuberculin test and poison ivy
C) Reaction to penicillin
D) Hay fever

A

Tuberculin test and poison ivy

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154
Q

What occurs during immediate hypersensitivity (Type 1)? A) Release of vasoactive products from IgE-coated mast cells B) Release of cytokines from Th1 cells

C) Formation of immune complexes with IgG D) None of the above

A

Release of vasoactive products from IgE-coated mast cells

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155
Q

What are the major symptoms of Type 1 hypersensitivity? A) Swelling, pain, and constriction of smooth muscles
B) Swelling and blood vessel constriction
C) Difficulty in breathing and inflammation of joints
D) None of the above

A

Swelling, pain, and constriction of smooth muscles

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156
Q

What is the role of epinephrine (EpiPen) in Type 1 hypersensitivity reactions? A) It dilates blood vessels to reduce swelling
B) It constricts blood vessels to prevent bleeding
C) It relaxes smooth muscles of the bronchioles to improve breathing
D) All of the above

A

It relaxes smooth muscles of the bronchioles to improve breathing

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157
Q

What is a characteristic of Delayed-Type Hypersensitivity (DTH)? A) Immediate reaction mediated by IgE antibodies
B) Cell-mediated hypersensitivity causing tissue damage
C) Caused by antigen-antibody complexes in the bloodstream
D) None of the above

A

Cell-mediated hypersensitivity causing tissue damage

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158
Q

Which of the following is a symptom of Delayed-Type Hypersensitivity (DTH)? A) Poison ivy blisters
B) Swelling of the face
C) Severe itching and rash
D) None of the above

A

Severe itching and rash

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159
Q

What type of cells are primarily involved in Delayed-Type Hypersensitivity (DTH)? A) T helper 1 (Th1) cells
B) T cytotoxic (Tc) cells
C) B cells
D) Neutrophils

A

T helper 1 (Th1) cells

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160
Q

Which of the following is a typical antigen involved in Type 4 hypersensitivity?

A) Microbes, self-antigens, and chemicals that bind to skin B) Bee venom and pollen
C) Antigens on the surface of red blood cells
D) Antibodies against soluble antigens

A

Microbes, self-antigens, and chemicals that bind to skin

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161
Q

What is the mechanism behind Type 2 hypersensitivity?
A) IgE antibodies bind to mast cells, causing degranulation
B) Antigen-antibody complexes deposit in tissues, causing inflammation
C) IgG or IgM antibodies bind to cell surface antigens, leading to cell destruction D) None of the above

A

IgG or IgM antibodies bind to cell surface antigens, leading to cell destruction

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162
Q

What is a common example of Type 2 hypersensitivity? A) Penicillin-induced hemolysis
B) Contact dermatitis
C) Systemic lupus erythematosus
D) Tuberculin test

A

Penicillin-induced hemolysis

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163
Q

In Type 3 hypersensitivity, where do the antigen-antibody complexes typically deposit? A) Skin and respiratory tract
B) Kidneys, joints, and blood vessels
C) Heart and lungs
D) Lymph nodes

A

Kidneys, joints, and blood vessels

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164
Q

Which of the following is an example of a Type 3 hypersensitivity reaction? A) Rheumatoid arthritis
B) Poison ivy
C) Bee sting reaction
D) Asthma

A

Rheumatoid arthritis

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165
Q

What occurs during a Type 3 hypersensitivity reaction?
A) Antigen-antibody complexes trigger complement activation and inflammation B) T helper cells activate macrophages to kill infected cells
C) IgE antibodies bind to mast cells, leading to histamine release
D) All of the above

A

Antigen-antibody complexes trigger complement activation and inflammation

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166
Q

What autoimmune condition is commonly associated with Type 3 hypersensitivity? A) Rheumatoid arthritis
B) Systemic lupus erythematosus (SLE)
C) Multiple sclerosis
D) Type 1 diabetes

A

Systemic lupus erythematosus (SLE)

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167
Q

Which of the following best describes Type 2 hypersensitivity?
A) IgE-mediated response leading to immediate degranulation of mast cells
B) Antibodies bind to antigens on cell surfaces, leading to complement activation

C) Immune complexes cause inflammation and tissue damage D) T-cell activation leads to chronic inflammation

A

Antibodies bind to antigens on cell surfaces, leading to complement activation

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168
Q

What is a common cause of tissue damage in Type 3 hypersensitivity? A) Complement activation and deposition of immune complexes in tissues B) T-cell activation of macrophages
C) Activation of mast cells and release of histamine
D) IgE binding to allergens

A

Complement activation and deposition of immune complexes in tissues

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169
Q

What causes autoimmune diseases?
A) T and B cells activated to produce immune reactions against self proteins B) Genetic mutations in immune cells
C) Overproduction of cytokines
D) None of the above

A

T and B cells activated to produce immune reactions against self proteins

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170
Q

Which of the following autoimmune conditions involves antibodies interacting with self antigens?
A) Allergic encephalitis
B) Type 1 diabetes mellitus C) Both A and B
D) None of the above

A

Both A and B

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171
Q

Which organ is primarily affected in Type 1 diabetes mellitus? A) Liver
B) Pancreas
C) Kidneys
D) Heart

A

Pancreas

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172
Q

What is the mechanism behind Type 1 diabetes mellitus? A) Autoantibodies against beta cells of the pancreas
B) Cell-mediated destruction of pancreatic beta cells
C) Both A and B
D) Inflammatory response in the pancreas

A

Both A and B

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173
Q

What is the primary organ affected by rheumatoid arthritis? A) Heart
B) Lungs
C) Cartilage in the major joints
D) Kidneys

A

Cartilage in the major joints

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174
Q

Which type of hypersensitivity is involved in the mechanism of rheumatoid arthritis? A) Type I hypersensitivity
B) Type II hypersensitivity
C) Type III hypersensitivity
D) Type IV hypersensitivity

A

Type III hypersensitivity

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175
Q

In Hashimoto’s disease, what is the mechanism behind thyroid destruction? A) Autoantibodies against thyroid surface antigen
B) T-cell mediated destruction of thyroid cells
C) Autoantibodies against thyroid-stimulating hormone
D) Activation of mast cells in the thyroid

A

Autoantibodies against thyroid surface antigen

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176
Q

Which autoimmune disease is characterized by the formation of autoantibodies against DNA, cardiolipin, and blood clotting proteins?
A) Rheumatoid arthritis
B) Systemic lupus erythematosus C) Type 1 diabetes mellitus
D) Hashimoto’s disease

A

Systemic lupus erythematosus

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177
Q

What is the main mechanism behind systemic lupus erythematosus (SLE)?
A) Autoantibodies against thyroid antigens
B) Formation of immune complexes involving DNA and other proteins C) T-cell mediated destruction of joint cartilage
D) Activation of complement by autoantibodies

A

Formation of immune complexes involving DNA and other proteins

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178
Q

Which of the following is a common feature of autoimmune diseases? A) Activation of immune responses against self proteins
B) Damage to host tissues
C) Both A and B
D) None of the above

A

Both A and B

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179
Q

What is a characteristic of superantigens?
A) They activate a normal number of T cells
B) They activate more T cells than a normal immune response C) They suppress T cell activation
D) They directly kill infected cells

A

They activate more T cells than a normal immune response

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180
Q

Which of the following is a source of superantigens? A) Only bacteria
B) Only viruses
C) Both viruses and bacteria
D) T cells themselves

A

Both viruses and bacteria

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181
Q

What is the consequence of superantigen activation in T cells? A) A localized immune response
B) A systemic inflammatory response
C) Immediate clearance of pathogens
D) Suppression of immune system function

A

A systemic inflammatory response

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182
Q

Immunodeficiency is a broad term referring to: A) An overactive immune response
B) A deficiency in immune system reactions
C) Normal immune system functioning
D) Excessive T cell activation

A

A deficiency in immune system reactions

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183
Q

Which of the following describes individuals with B cell deficiencies? A) Prone to viral infections and cancers
B) Prone to bacterial infections
C) Not susceptible to any infections
D) Prone to fungal infections

A

Prone to bacterial infections

184
Q

What type of infections are individuals with T cell deficiencies more susceptible to? A) Bacterial infections
B) Fungal infections
C) Viral infections and cancers D) All of the above

A

Viral infections and cancers

185
Q

Which of the following is a characteristic of Severe Combined Immunodeficiency (SCID)? A) Deficiency of both B and T cells
B) Deficiency of only B cells
C) A deficiency of only T cells
D) Overactive immune response

A

Deficiency of both B and T cells

186
Q

What is the nickname for Severe Combined Immunodeficiency (SCID) due to its restricted life requirements?
A) “Bubble Boy” syndrome
B) “T Cell Deficiency” syndrome
C) “AIDS” syndrome
D) “Autoimmune Disorder” syndrome

A

“Bubble Boy” syndrome

187
Q

Which virus causes Acquired Immunodeficiency Syndrome (AIDS)? A) Hepatitis B virus
B) Epstein-Barr virus
C) HIV (Human Immunodeficiency Virus)
D) Human papillomavirus (HPV)

A

HIV (Human Immunodeficiency Virus)

188
Q

What immune deficiency is seen in AIDS patients? A) Deficiency of CD8+ T cells
B) Deficiency of CD4+ T cells
C) Deficiency of B cells
D) Deficiency of neutrophils

A

Deficiency of CD4+ T cells

189
Q

Which of the following is a characteristic of vaccines against bacterial diseases like anthrax and tetanus?
A) Live attenuated bacteria
B) Killed bacteria or toxoid
C) Recombinant DNA vaccine D) None of the above

A

Killed bacteria or toxoid

190
Q

Which type of vaccine is used for the prevention of hepatitis B? A) Recombinant DNA vaccine or inactivated virus
B) Attenuated virus
C) Conjugate vaccine
D) Killed bacteria

A

Recombinant DNA vaccine or inactivated virus

191
Q

Which vaccine is made from a polysaccharide-toxoid conjugate to enhance T cell response? A) Pneumococcal vaccine
B) Diphtheria vaccine
C) Polio vaccine
D) Yellow fever vaccine

A

Pneumococcal vaccine

192
Q

Why are live attenuated virus vaccines often more effective than inactivated ones? A) They require fewer booster doses
B) They stimulate both the humoral and cell-mediated immune responses
C) They are easier to produce
D) They are cheaper

A

They stimulate both the humoral and cell-mediated immune responses

193
Q

What is the primary advantage of synthetic and genetically engineered vaccines? A) They are less expensive to produce
B) They provide stronger immune responses compared to live attenuated vaccines C) They are made from the entire microorganism
D) They use engineered antigenic components to stimulate the immune response

A

They use engineered antigenic components to stimulate the immune response

194
Q

Which of the following vaccines is made from a genetically engineered DNA plasmid? A) Hepatitis A
B) Pneumococcal vaccine
C) DNA vaccine
D) Smallpox vaccine

A

DNA vaccine

195
Q

Which of the following is a key feature of conjugate vaccines?
A) They are composed of live bacteria
B) They combine a small antigenic protein with a larger carrier protein
C) They use inactivated virus particles
D) They are primarily used for viral diseases

A

They combine a small antigenic protein with a larger carrier protein

196
Q

What is the key reason why vaccines against viral diseases, like polio and rabies, are crucial despite the lack of effective antiviral medications?
A) Vaccines provide immunity before infection occurs
B) Viral diseases are more difficult to treat with antibiotics C) Antivirals are effective in all cases
D) Vaccines are cheaper than antiviral medications

A

Vaccines provide immunity before infection occurs

197
Q

What type of vaccine is used for measles and mumps? A) Inactivated virus
B) Attenuated virus
C) Recombinant DNA vaccine
D) Conjugate vaccine

A

Attenuated virus

198
Q

What is the role of booster immunizations in vaccination schedules?
A) They help to induce primary immune responses
B) They increase the antibody titer by stimulating a secondary immune response C) They are used to prevent disease in the elderly
D) None of the above

A

They increase the antibody titer by stimulating a secondary immune response

199
Q

Which of the following best describes the purpose of anticancer vaccines? A) To stimulate the body’s natural immune response to cancer cells
B) To prevent the activation of immune cells in the body
C) To treat viral infections associated with cancer
D) To neutralize tumor-promoting cytokines

A

To stimulate the body’s natural immune response to cancer cells

200
Q

Prophylactic anticancer vaccines are designed to target which of the following?
A) Tumor cells directly
B) Oncogenic pathogens such as viruses
C) The immune system’s ability to produce antibodies D) Cancer stem cells

A

Oncogenic pathogens such as viruses

201
Q

Which type of anticancer vaccine is designed to treat existing cancer by stimulating the body’s immune system?
A) Therapeutic vaccines B) Prophylactic vaccines C) Vaccine adjuvants
D) Passive vaccines

A

Therapeutic vaccines

202
Q

What is the primary goal of checkpoint inhibitors in cancer immunotherapy?
A) To neutralize tumor cells directly
B) To prevent the activation of the immune system
C) To prevent the neutralization of cytotoxic T cells and stimulate their tumor-killing activity D) To inhibit the growth of cancer cells by targeting oncogenes

A

To prevent the neutralization of cytotoxic T cells and stimulate their tumor-killing activity

203
Q

Which checkpoint inhibitor drug targets the PD-1 receptor on T cells or its ligand PD-L1 on cancer cells?
A) Trastuzumab
B) Pembrolizumab (Keytruda®) C) Ipilimumab (Yervoy®)
D) Rituximab

A

Pembrolizumab (Keytruda®)

204
Q

What is the primary mechanism of action of Pembrolizumab (Keytruda®)? A) It inhibits the expression of tumor suppressor genes
B) It stimulates the production of antibodies against cancer cells
C) It blocks the PD-1/PD-L1 interaction to restore T cell activity against tumors D) It induces cancer cell apoptosis through immune activation

A

It blocks the PD-1/PD-L1 interaction to restore T cell activity against tumors

205
Q

In adoptive T cell transfer (ACT) therapy, what is the primary focus? A) Boosting the production of antibodies
B) Harnessing the tumor-targeting abilities of T cells
C) Suppressing the immune response to cancer
D) Enhancing the function of dendritic cells in antigen presentation

A

Harnessing the tumor-targeting abilities of T cells

206
Q

What are the two main approaches developed for ACT therapy?
A) Tumor-infiltrating lymphocytes (TILs) and monoclonal antibodies
B) Tumor-infiltrating lymphocytes (TILs) and chimeric antigen receptor (CAR) T cells C) Chimeric antigen receptor (CAR) T cells and dendritic cell vaccines
D) T cells and B cells activated by checkpoint inhibitors

A

Tumor-infiltrating lymphocytes (TILs) and chimeric antigen receptor (CAR) T cells

207
Q

How does the gut microbiome affect the efficacy of cancer immunotherapy? A) It has no effect on immunotherapy outcomes
B) The composition of gut microbes can influence the immune system’s response to treatment C) Only harmful bacteria can improve the efficacy of treatment
D) It directly alters cancer cell metabolism

A

The composition of gut microbes can influence the immune system’s response to treatment

208
Q

What is the goal of studying the gut microbiome in relation to immunotherapy? A) To identify bacteria that suppress immune function
B) To determine which microbes enhance the effectiveness of immunotherapies C) To formulate antibiotics that neutralize harmful bacteria
D) To develop probiotic treatments that prevent cancer

A

To determine which microbes enhance the effectiveness of immunotherapies

209
Q

What is the primary feature that makes antibiotics useful for treating infections?
A) They are produced by fungi and bacteria
B) They exhibit selective toxicity, targeting pathogens while leaving host cells unharmed C) They are synthetic compounds
D) They are effective against all microbes, including viruses

A

They exhibit selective toxicity, targeting pathogens while leaving host cells unharmed

210
Q

Which of the following best describes the classification of antibiotics? A) Antibiotics are classified by their origin (natural or synthetic)
B) Antibiotics are classified by their mechanism of action
C) Antibiotics are classified by their side effects
D) Antibiotics are classified based on the organisms they target

A

Antibiotics are classified by their mechanism of action

211
Q

What is the key difference between broad-spectrum and narrow-spectrum antibiotics? A) Broad-spectrum antibiotics target only one type of bacteria
B) Narrow-spectrum antibiotics are effective against both gram-positive and gram-negative bacteria
C) Broad-spectrum antibiotics target both gram-positive and gram-negative bacteria, while narrow-spectrum antibiotics are effective against only certain groups of bacteria
D) Narrow-spectrum antibiotics are more toxic to host cells

A

Broad-spectrum antibiotics target both gram-positive and gram-negative bacteria, while narrow-spectrum antibiotics are effective against only certain groups of bacteria

212
Q

Which of the following antibiotics are primarily used to target bacterial cell wall synthesis? A) β-lactam antibiotics (e.g., penicillin, cephalosporins)
B) Aminoglycosides (e.g., streptomycin)
C) Macrolides (e.g., azithromycin)
D) Tetracyclines (e.g., doxycycline)

A

β-lactam antibiotics (e.g., penicillin, cephalosporins)

213
Q

Which of the following is NOT a feature of β-lactam antibiotics?
A) They are effective against both gram-positive and gram-negative bacteria B) They contain a β-lactam ring structure
C) They are effective against Archaea and Eukaryotes
D) They are among the most widely used antibiotics globally

A

They are effective against Archaea and Eukaryotes

214
Q

Which of the following is NOT a target of β-lactam antibiotics? A) Peptidoglycan synthesis
B) Protein synthesis
C) Bacterial cell wall
D) They do not target Eukaryotic cells

A

Protein synthesis

215
Q

Which type of bacteria are most likely affected by β-lactam antibiotics? A) Gram-positive bacteria only
B) Gram-negative bacteria only
C) Both gram-positive and gram-negative bacteria
D) Archaea

A

Both gram-positive and gram-negative bacteria

216
Q

Which of the following antibiotics is a macrolide, commonly used in clinical practice? A) Erythromycin
B) Penicillin
C) Cephalosporin D) Streptomycin

A

Erythromycin

217
Q

What percentage of global antibiotic usage is attributed to agricultural (animal) use? A) 36%
B) 64%
C) 11%
D) 13%

A

64%

218
Q

Which of the following antibiotics targets protein synthesis by binding to the bacterial ribosome’s 30S or 50S subunits?
A) Tetracycline
B) Rifampin
C) Polymyxins D) Sulfonamides

A

Tetracycline

219
Q

Why do antibiotics that target protein synthesis typically exhibit selective toxicity? A) Bacterial ribosomes are identical to eukaryotic ribosomes
B) Eukaryotic cells have no ribosomes
C) Bacterial ribosomes differ from eukaryotic ribosomes
D) Eukaryotic cells have more efficient ribosomes than bacteria

A

Bacterial ribosomes differ from eukaryotic ribosomes

220
Q

What is the mechanism of resistance to tetracycline? A) Mutation in RNA polymerase
B) Efflux pump that removes the antibiotic
C) Mutation in the 30S ribosomal subunit
D) Altered target site for folic acid synthesis

A

Efflux pump that removes the antibiotic

221
Q

Which antibiotic class is known for blocking the exit tunnel in the bacterial ribosome, preventing peptide chain elongation?
A) Aminoglycosides
B) Macrolides
C) Tetracyclines D) Quinolones

A

Macrolides

222
Q

Which class of antibiotic inhibits DNA gyrase and is effective against both gram-positive and gram-negative bacteria?
A) Macrolides ( erythromycin)
B) aminoglycoside (Streptomycin)
C) Quinolones (ciprofloxacin, nalidixic acid, chloroquine(as antimalarial agent) D) Polymyxins (Polymyxin B)
E) sulfa drugs or sulfonamide (trimetoprim)

A

Quinolones

223
Q

How do quinolones, such as nalidixic acid, interfere with bacterial DNA? A) By inhibiting RNA polymerase
B) By inhibiting DNA gyrase, preventing supercoiling
C) By inhibiting ribosome function
D) By preventing protein synthesis

A

By inhibiting DNA gyrase, preventing supercoiling

224
Q

Which of the following antibiotics interferes with RNA transcription by inhibiting RNA polymerase?
A) Tetracycline
B) Rifampin
C) Penicillin
D) Streptomycin

A

Rifampin

225
Q

What is the mechanism of resistance to quinolones? A) Mutation in the DNA gyrase gene
B) Efflux pumps in bacterial membranes
C) Modification of ribosomal subunits
D) Production of protective proteins for ribosomes

A

Mutation in the DNA gyrase gene

226
Q

Which drug class inhibits folic acid synthesis by mimicking a growth factor, preventing bacterial cell division?
A) Sulfonamides
B) Isoniazid
C) Rifampin D) Macrolides

A

Sulfonamides

227
Q

Which of the following antibiotics inhibits mycolic acid synthesis in Mycobacterium species? A) Rifampin
B) Isoniazid
C) Tetracycline
D) Polymyxin

A

Isoniazid

228
Q

What is the mechanism of action of platensimycin? A) Inhibition of protein synthesis
B) Inhibition of lipid biosynthesis
C) Inhibition of DNA replication
D) Disruption of bacterial cell membrane

A

Inhibition of lipid biosynthesis

229
Q

Which antibiotic disrupts bacterial cell membranes and is effective against multi-drug resistant organisms like MRSA?
A) Isoniazid
B) Rifampin
C) Polymyxins D) Platensimycin

A

Polymyxins

230
Q

What do most antiviral drugs target? A) Viral structures
B) Viral RNA
C) Host structures D) Viral proteins

A

Host structures

231
Q

Which class of antiviral drugs does AZT (zidovudine) belong to? A) Non-nucleoside reverse transcriptase inhibitors (NNRTIs)
B) Protease inhibitors
C) Nucleoside reverse transcriptase inhibitors (NRTIs)
D) Fusion inhibitors

A

Nucleoside reverse transcriptase inhibitors (NRTIs)

232
Q

What is the main action of Nucleoside reverse transcriptase inhibitors (NRTIs)? A) Inhibit viral RNA replication
B) Block reverse transcriptase and production of viral DNA
C) Prevent the fusion of the virus with the host cell
D) Inhibit protease enzymes

A

Block reverse transcriptase and production of viral DNA

233
Q

How do Non-nucleoside reverse transcriptase inhibitors (NNRTIs) work? A) They inhibit viral DNA polymerase
B) They block reverse transcriptase by binding directly to the enzyme
C) They incorporate into viral RNA
D) They prevent viral fusion with the host cell

A

They block reverse transcriptase by binding directly to the enzyme

234
Q

What is the primary function of fusion inhibitors in antiviral therapy? A) Block reverse transcription
B) Prevent the fusion of the virus with the host cell
C) Inhibit protease activity
D) Block viral DNA replication

A

Prevent the fusion of the virus with the host cell

235
Q

Why can antiviral drugs lead to toxicity in the host? A) They target only viral structures
B) They interfere with normal host DNA replication
C) They often lead to toxicity in the host
D) They inhibit host protein synthesis

A

They often lead to toxicity in the host

236
Q

What is the difference between NRTIs and NNRTIs?
A) NRTIs prevent viral RNA synthesis, while NNRTIs block viral DNA production
B) NRTIs block reverse transcriptase by incorporating into DNA, while NNRTIs inhibit reverse transcriptase directly
C) NRTIs prevent fusion, while NNRTIs inhibit viral RNA transcription
D) NRTIs inhibit protease, while NNRTIs block reverse transcriptase

A

NRTIs block reverse transcriptase by incorporating into DNA, while NNRTIs inhibit reverse transcriptase directly

237
Q

What enzyme do most HIV antiviral drugs target? A) Reverse transcriptase
B) Integrase
C) Protease
D) RNA polymerase

A

Reverse transcriptase

238
Q

Why are traditional antibacterial agents generally ineffective against fungi? A) Fungi lack a cell wall
B) Fungi are eukaryotic cells
C) Fungi do not have ribosomes
D) Fungi do not have a plasma membrane

A

Fungi are eukaryotic cells

239
Q

What unique structure in fungal cells makes them a good target for antifungal drugs? A) Mitochondria
B) Chitin cell wall and ergosterol in the membrane
C) DNA in the nucleus
D) Ribosomal RNA

A

Chitin cell wall and ergosterol in the membrane

240
Q

Which component of the fungal cell membrane is targeted by ergosterol inhibitors? A) Phospholipids
B) Chitin
C) Ergosterol
D) Protein receptors

A

Ergosterol

241
Q

Which class of antifungal drugs targets ergosterol in the fungal membrane? A) Azoles and Polyenes
B) Echinocandins
C) Allylamines
D) Griseofulvin

A

Azoles and Polyenes

242
Q

What is the target of cell wall inhibitors in antifungal therapy? A) 1,3 β-D glucan synthase
B) DNA polymerase
C) Chitin synthase
D) Ergosterol

A

1,3 β-D glucan synthase

243
Q

Which antifungal drug class is used to treat Candida infections by inhibiting cell wall synthesis?
A) Echinocandins
B) Azoles
C) Polyenes D) Allylamines

A

Echinocandins

244
Q

What process is disrupted by antifungal drugs that target microtubules? A) Protein synthesis
B) Mitosis
C) DNA replication
D) Membrane fluidity

A

Mitosis

245
Q
  1. Which of the following is a common mechanism of antifungal resistance? A) Overproduction of ergosterol
    B) Increased chitin synthesis
    C) Inhibition of ribosomal activity
    D) Enhanced DNA repair mechanisms
A

Overproduction of ergosterol

246
Q

Which antifungal drug is used to target fungal mitosis by disrupting microtubule aggregation? A) Griseofulvin
B) Caspofungin
C) Fluconazole
D) Amphotericin B

A

Griseofulvin

247
Q

Which of the following drugs is specifically used to treat fungal infections through its action on DNA synthesis?
A) Griseofulvin
B) Flucytosine
C) Itraconazole D) Ketoconazole

A

Flucytosine

248
Q

Which of the following drugs is primarily used to combat malaria? A) Albendazole
B) Ivermectin
C) Chloroquine
D) Flucytosine

A

Chloroquine

249
Q

How does albendazole work to combat parasitic worms?
A) Inhibits cell wall synthesis
B) Binds to the beta-tubulin protein, causing immobilization and death C) Disrupts DNA replication
D) Inhibits protein synthesis

A

Binds to the beta-tubulin protein, causing immobilization and death

250
Q

What is the primary mechanism of action of ivermectin?
A) Inhibits the synthesis of folic acid
B) Inhibits mitosis in parasitic cells
C) Modulates glutamate-gated chloride channels leading to cell hyperpolarization D) Binds to ergosterol in the fungal membrane

A

Modulates glutamate-gated chloride channels leading to cell hyperpolarization

251
Q

Which of the following animals is ivermectin most commonly used for in anti-worming treatments?
A) Horses and cats
B) Humans
C) Dogs and birds D) Cattle and pigs

A

Horses and cats

252
Q

Which drug targets beta-tubulin in parasitic worms, immobilizing them and causing death? A) Chloroquine
B) Ivermectin
C) Albendazole
D) Griseofulvin

A

Albendazole

253
Q

Penicillin is _____ by nature A) B-lactam
B) Quinolone C) Sulfa drug D) Tetracycline

A

B-lactam

254
Q

Some antibiotics interfere with bacterial DNA synthesis by interacting with A) Ribosome
B) RNApolymerase C) DNA gyrase
D) None of the above

A

DNA gyrase

255
Q

What is the mechanism of action of tetracycline?
A. Bindsto30Sribosomalsubunitandinterruptsproteinsynthesis
B. BindstoDNAgyraseandinterfereswithDNAsynthesis
C. BindstotheenzymethatsynthesizesB12
D. Bindstothepenicillinbindingproteinandinterfereswithcellwallsynthesis

A

Binds to 30S ribosomal subunit and interrupts protein synthesis

256
Q

Substances that are naturally produced by certain microorganisms that can inhibit or destroy other microorganisms are called_________.
A) antibiotics
B) narrow-spectrum drugs
C) semisynthetic drugs
D) synthetic drugs
E) broad-spectrum drugs

A

Antibiotics

257
Q

Which of the following would be useful for treating fungal infections like Candida? A. Tetracycline
B. Penicillin
C. Azole
D. AZT

A

Azole

258
Q

What antibiotics and its chemical nature are mismatched?
A. Macrolide - Streptomycin
B. B-lactam- penicillin, amoxicillin
C. Quinolone - nalidixic acid, chloroquine
D. Sulfonamide (or sulfa-drug) - sulfamethoxazole, trimetoprim

A

Macrolide - Streptomycin

259
Q

WHich of the following would be useful for treating HIV patients?
A. AZT and NRTI
B. Tetracycline
C. Azoles

A

AZT and NRTI

260
Q

What is the primary focus of clinical microbiology?
a) Developing vaccines
b) Diagnosing infectious diseases and advising on treatment c) Studying genetic disorders
d) Monitoring environmental microbes

A

Diagnosing infectious diseases and advising on treatment

261
Q

How are clinical laboratories classified in terms of safety? a) Based on the type of equipment used
b) According to their biosafety levels (BSL-1 to BSL-4)
c) Based on the size of the laboratory
d) By the number of personnel employed

A

According to their biosafety levels (BSL-1 to BSL-4)

262
Q

What is the safest biosafety level in a clinical laboratory? a) BSL-1
b) BSL-2
c) BSL-3
d) BSL-4

A

BSL-1

263
Q

What percentage of healthcare-associated infections (HAI) are attributed to surgical site infections?
a) 10%
b) 22%
c) 30% d) 50%

A

22%

264
Q

Which of the following is a key measure to control healthcare-associated infections? a) Minimizing patient interaction
b) Applying basic aseptic techniques
c) Using only antibiotics for treatment
d) Increasing the number of hospital personnel

A

Applying basic aseptic techniques

265
Q

What makes healthcare-associated infections challenging to treat? a) They spread too quickly
b) They are often resistant to antibiotics
c) They occur only in isolated cases
d) They are caused by rare pathogens

A

They are often resistant to antibiotics

266
Q

What is the second most common type of healthcare-associated infection after surgical site infections?
a) Gastrointestinal infections
b) Respiratory infections
c) Urinary infections
d) Bloodstream infections

A

Respiratory infections

267
Q

Where do healthcare-associated infections originate from? a) Only from patients
b) Only from hospital personnel
c) From patients or hospital personnel
d) From environmental sources only

A

From patients or hospital personnel

268
Q

What is the first step in diagnosing an infectious disease in the laboratory? a) Culturing the pathogen in a pure medium
b) Identifying pathogen genes using molecular assays
c) Collecting samples such as blood, urine, or tissue
d) Applying antibiotics to the sample

A

Collecting samples such as blood, urine, or tissue

269
Q

Which assay is used to detect antibodies against a suspected pathogen? a) Antigen assays
b) Immunological assays
c) Molecular assays
d) Growth-dependent microbiology

A

Immunological assays

270
Q

What type of media is used to enrich the growth of fastidious organisms like Neisseria gonorrhoeae?
a) General-purpose media
b) Selective media
c) Enriched selective media d) Differential media

A

Enriched selective media

271
Q

What is the purpose of antibiotics in Modified Thayer-Martin (MTM) agar? a) To enhance the growth of all bacteria
b) To inhibit the growth of non-target organisms
c) To differentiate bacterial colonies
d) To support anaerobic bacteria

A

To inhibit the growth of non-target organisms

272
Q

What does sensitivity in a diagnostic test indicate? a) Ability to identify the correct pathogen
b) Minimizing false positives
c) Minimum amount of pathogen needed for detection d) Growth of colonies on differential media

A

Minimum amount of pathogen needed for detection

273
Q

How can Neisseria gonorrhoeae be identified microscopically? a) By observing growth on blood agar
b) Through colony morphology on EMB agar
c) Using a selective medium like MTM agar
d) By direct microscopic examination of tissue samples

A

By direct microscopic examination of tissue samples

274
Q

What distinguishes differential media from other types of media? a) Inhibits certain bacteria while allowing others to grow
b) Enriches growth for fastidious bacteria
c) Identifies organisms based on growth appearance
d) Contains general nutrients for a variety of microbes

A

Identifies organisms based on growth appearance

275
Q

What is an example of a bacterium that exhibits a greenish sheen on EMB agar?

a) Pseudomonas aeruginosa b) Escherichia coli
c) Neisseria gonorrhoeae
d) Staphylococcus aureus

A

E. coli

276
Q

Why is EMB agar considered both selective and differential?
a) It inhibits Gram-positive bacteria and differentiates between gram negative lactose fermenters b) It contains antibiotics for selective growth
c) It enhances the growth of all organisms
d) It supports anaerobic growth while differentiating bacteria

A

It inhibits Gram-positive bacteria and differentiates between gram negative lactose fermenters

277
Q

What does specificity in a diagnostic test measure? a) The pathogen’s growth speed
b) Ability to minimize false positives
c) The minimum pathogen quantity needed for detection d) The effectiveness of enriched media

A

Ability to minimize false positives

278
Q

What is bacteremia?
a) The presence of a large number of bacteria in the blood
b) The presence of small numbers of bacteria in the blood
c) An infection limited to cerebrospinal fluid
d) A severe bacterial infection causing systemic inflammation

A

The presence of small numbers of bacteria in the blood

279
Q

How is septicemia defined?
a) The presence of bacteria in the blood without symptoms
b) A blood infection characterized by bacterial colonization and high bacterial numbers c) A fungal infection of the bloodstream
d) The absence of bacteria in the blood

A

A blood infection characterized by bacterial colonization and high bacterial numbers

280
Q

What is the standard volume of blood drawn for blood cultures? a) 5 to 10 milliliters
b) 10 to 20 milliliters
c) 15 to 30 milliliters
d) 20 to 40 milliliters

A

10 to 20 milliliters

281
Q

Why are two bottles used in blood cultures? a) To separate blood components
b) To culture aerobic and anaerobic bacteria c) To test for bacterial and viral pathogens
d) To reduce contamination risks

A

To culture aerobic and anaerobic bacteria

282
Q

What method is used to monitor bacterial growth in an automated blood culture system? a) Microscopic examination
b) Measuring turbidity, CO2 production, or fluorescence
c) Staining techniques
d) DNA sequencing

A

Measuring turbidity, CO2 production, or fluorescence

283
Q

What makes urinary tract infections (UTIs) common in women? a) Frequent exposure to antibiotics
b) Proximity of the urethra to other anatomical structures
c) Inability to produce acid in the urinary tract d) Absence of normal flora in the urinary tract

A

Proximity of the urethra to other anatomical structures

284
Q

Which type of medium is used to identify E. coli in urinary cultures? a) General-purpose media
b) Selective media like MacConkey agar
c) Differential media for sugar fermentation
d) Blood agar

A

Selective media like MacConkey agar

285
Q

What is the purpose of differential media?
a) To inhibit the growth of specific organisms
b) To differentiate between bacteria based on growth and appearance c) To enhance the growth of fastidious organisms
d) To identify antibiotic resistance

A

To differentiate between bacteria based on growth and appearance

286
Q

How is acid production in sugar fermentation tests indicated? a) Formation of gas bubbles
b) Change in media color to yellow
c) Blackening of the agar
d) Turbidity increase in the medium

A

Change in media color to yellow

287
Q

What does the blackening of the agar in a triple-sugar iron (TSI) test indicate? a) Gas production due to fermentation
b) Hydrogen sulfide formation
c) Acid production from glucose fermentation
d) Inhibition of bacterial growth

A

Hydrogen sulfide formation

288
Q

What does the breaking up of the agar in a TSI test indicate? a) Fermentation of lactose or sucrose
b) Hydrogen sulfide production
c) Gas production during sugar fermentation
d) Growth without fermentation

A

Gas production during sugar fermentation

289
Q

What is the primary advantage of miniaturized media kits in clinical microbiology? a) They allow faster culturing of bacteria
b) They facilitate simultaneous testing of many biochemical reactions
c) They eliminate the need for manual analysis
d) They improve the growth of anaerobic organisms

A

They facilitate simultaneous testing of many biochemical reactions

290
Q

What kind of test can differentiate enteric bacteria based on sugar fermentation patterns? a) MacConkey agar test
b) Triple-sugar iron (TSI) test
c) Blood culture analysis
d) Fluorescence-based automated systems

A

Triple-sugar iron (TSI) test

291
Q

Which bacterium typically ferments only glucose in a TSI test? a) Escherichia coli
b) Salmonella
c) Pseudomonas
d) Shigella

A

Shigella

292
Q

What is indicated by gas bubbles in a sugar fermentation test? a) No fermentation
b) Acid production
c) Gas production from sugar fermentation
d) Hydrogen sulfide formation

A

Gas production from sugar fermentation

293
Q

Why are urinary tract infections (UTIs) more common in women? a) Women have a stronger immune response
b) Proximity of the urethra to the anus
c) Higher resistance of bacteria in women
d) Increased hydration levels in women

A

Proximity of the urethra to the anus

294
Q

Which medium is specifically selective for culturing E. coli in urinary tract infections? a) Blood agar
b) MacConkey agar
c) Chocolate agar
d) Thayer–Martin agar

A

MacConkey agar

295
Q

What indicates acid production in a sugar fermentation test? a) Formation of gas bubbles
b) Media color changing to red

c) Media color changing to yellow d) Blackening of the agar

A

Media color changing to yellow

296
Q

What is the purpose of miniaturized media kits in microbiological testing? a) To isolate anaerobic bacteria
b) To simultaneously run multiple biochemical tests
c) To eliminate contamination during testing
d) To test antibiotic resistance

A

To simultaneously run multiple biochemical tests

297
Q

What characteristic result does Salmonella produce in a triple-sugar iron (TSI) agar test? a) Growth without fermentation
b) Hydrogen sulfide formation causing blackening
c) Fermentation of glucose only
d) Acid formation throughout the slant

A

acid formation throughout the slant

298
Q

Which bacterium typically ferments all three sugars in the TSI test with gas production? a) Pseudomonas
b) Shigella
c) Salmonella
d) Escherichia coli

A

e coli

299
Q

What medium is commonly used to identify MRSA in wound cultures? a) Blood agar
b) Chromogenic agar
c) Selective agar for anaerobes
d) Thayer–Martin agar

A

Chromogenic agar

300
Q

Which medium is selective for Neisseria gonorrhoeae in genital cultures? a) Blood agar
b) Chocolate agar
c) Thayer–Martin agar
d) MacConkey agar

A

Thayer–Martin agar

301
Q

What is the purpose of the Minimum Inhibitory Concentration (MIC) test?
a) To assess bacterial growth rates
b) To determine the smallest antibiotic concentration to inhibit bacterial growth c) To evaluate aerobic bacterial metabolism
d) To measure acid production in sugar fermentation

A

To determine the smallest antibiotic concentration to inhibit bacterial growth

302
Q

What is the principle behind the Kirby-Bauer test? a) Detecting sugar fermentation
b) Measuring gas production
c) Assessing inhibition zones formed by antibiotics
d) Identifying obligate anaerobes

A

Assessing inhibition zones formed by antibiotics

303
Q

Immunoassays are used for:
a) Identifying pathogens using in vitro tests

b) Measuring cell size
c) Observing bacterial motility
d) Determining pH levels in blood

A

Identifying pathogens using in vitro tests

304
Q

What does an elevated antibody titer indicate? a) Recovery from an infection
b) An ongoing infection or exposure to a pathogen c) Complete elimination of the pathogen
d) Autoimmune diseases

A

An ongoing infection or exposure to a pathogen

305
Q

Monoclonal antibodies (mAbs) are produced by: a) Isolating single clones of T cells
b) Fusing B cells with cancer cells
c) Amplifying DNA using PCR
d) Purifying blood plasma proteins

A

Fusing B cells with cancer cells

306
Q

Which of the following is NOT an application of monoclonal antibodies? a) Immunological typing of bacterial pathogens
b) Blood and tissue typing
c) DNA sequencing
d) Cancer detection and treatment

A

DNA sequencing

307
Q

Precipitation occurs when:
a) Antigen and antibody are at equivalent concentrations
b) Antibody binds to soluble antigen forming a visible clump c) Antigen and antibody react under UV light
d) Antigen breaks down into smaller molecules

A

Antigen and antibody are at equivalent concentrations

308
Q

What is a key feature of agglutination tests?
a) They require advanced laboratory equipment
b) They are rapid, sensitive, and inexpensive
c) They cannot be used for blood group identification d) They do not use antibodies

A

They are rapid, sensitive, and inexpensive

309
Q

Passive agglutination is:
a) The agglutination of soluble antibodies on red blood cells
b) Clumping of soluble antigens or antibodies adsorbed onto particles c) Less sensitive than direct agglutination

d) The reaction of fluorescent antigens

A

Clumping of soluble antigens or antibodies adsorbed onto particles

310
Q

In direct immunofluorescence, the antibody is: a) Nonfluorescent
b) Covalently linked to a fluorescent dye
c) Attached to an enzyme
d) Coupled to latex beads

A

Covalently linked to a fluorescent dye

311
Q

Fluorescent antibody assays are useful for diagnosing: a) Infectious diseases only
b) Noninfectious diseases like cancer
c) Both infectious and noninfectious diseases
d) Only bacterial infections

A

Both infectious and noninfectious diseases

312
Q

What is a primary difference between rapid tests and ELISA?
a) Rapid tests use fluorescent labels, while ELISA does not
b) Rapid tests provide results within minutes, while ELISA takes hours c) Rapid tests require a laboratory setting, while ELISA is point-of-care d) ELISA is less sensitive than rapid tests

A

Rapid tests provide results within minutes, while ELISA takes hours

313
Q

Rapid diagnostic tests detect antigens by: a) Measuring nucleic acid sequences
b) Observing visible clumping reactions
c) Using a colored molecule bound to a matrix d) Calculating antibody titers

A

Using a colored molecule bound to a matrix

314
Q

Nucleic acid hybridization involves:
a) Amplifying DNA using PCR
b) Detecting specific pathogen DNA using nucleic acid probes c) Counting microbes in a sample
d) Using antibodies for fluorescent labeling

A

Detecting specific pathogen DNA using nucleic acid probes

315
Q

What is the main function of RT-PCR?
a) Amplifying pathogen DNA
b) Detecting RNA viruses by converting RNA into cDNA c) Performing rapid antigen-antibody reactions
d) Measuring fluorescence in immunoassays

A

Detecting RNA viruses by converting RNA into cDNA

316
Q

Quantitative PCR (qPCR) is used to:
a) Detect insoluble complexes of antibodies and antigens b) Obtain a count of microbes in a sample
c) Identify blood group antigens
d) Measure antibody titers in serum

A

Obtain a count of microbes in a sample

317
Q

Which of the following assays can estimate the number of mRNA molecules in a sample? a) Passive agglutination
b) ELISA
c) Reverse transcription PCR (RT-PCR)
d) Precipitation tests

A

Reverse transcription PCR (RT-PCR)

318
Q

What stage of acute infection occurs when symptoms are at their peak? A) Incubation period
B) Acute period
C) Decline period
D) Convalescent period

A

Acute period

319
Q

What is a zoonosis?
A) A disease that only affects humans
B) A disease that primarily infects animals but can occasionally be transmitted to humans C) A disease that spreads through human-to-human transmission only
D) A disease caused by a microorganism that lives in the human gut

A

A disease that primarily infects animals but can occasionally be transmitted to humans

320
Q

Which of the following best distinguishes a mechanical vector from a biological vector?
A) A mechanical vector transmits the pathogen by carrying it on its body, while a biological vector involves pathogen replication inside the vector
B) A mechanical vector carries the pathogen inside its body, while a biological vector transmits it only on its surface
C) A biological vector only transmits bacteria, while a mechanical vector transmits viruses D) Both vectors involve pathogen replication inside the human host

A

A mechanical vector transmits the pathogen by carrying it on its body, while a biological vector involves pathogen replication inside the vector

321
Q

What is a common vehicle in disease transmission?
A) A living organism that carries the pathogen from one host to another B) A mode of transmission that involves direct contact between hosts C) A nonliving agent, such as water or food, that transmits pathogens D) A vector that transmits diseases only through the air

A

A nonliving agent, such as water or food, that transmits pathogens

322
Q

Which of the following is the most accurate description of the number of dead individuals in a population due to a specific disease?
A) Morbidity
B) Mortality rate
C) Prevalence rate
D) Incidence rate

A

Mortality rate

323
Q

What stage of acute infection occurs when symptoms are at their peak?
A) Incubation period
B) Acute period
C) Decline period
D) Convalescent period

A

Acute period

324
Q

What is a zoonosis?
A) A disease that only affects humans
B) A disease that primarily infects animals but can occasionally be transmitted to humans C) A disease that spreads through human-to-human transmission only
D) A disease caused by a microorganism that lives in the human gut

A

A disease that primarily infects animals but can occasionally be transmitted to humans

325
Q

Which of the following best distinguishes a mechanical vector from a biological vector?
A) A mechanical vector transmits the pathogen by carrying it on its body, while a biological vector involves pathogen replication inside the vector
B) A mechanical vector carries the pathogen inside its body, while a biological vector transmits it only on its surface
C) A biological vector only transmits bacteria, while a mechanical vector transmits viruses D) Both vectors involve pathogen replication inside the human host

A

A mechanical vector transmits the pathogen by carrying it on its body, while a biological vector involves pathogen replication inside the vector

326
Q

What is a common vehicle in disease transmission?
A) A living organism that carries the pathogen from one host to another B) A mode of transmission that involves direct contact between hosts C) A nonliving agent, such as water or food, that transmits pathogens D) A vector that transmits diseases only through the air

A

A nonliving agent, such as water or food, that transmits pathogens

327
Q

Which of the following is the most accurate description of the number of dead individuals in a population due to a specific disease?
A) Morbidity
B) Mortality rate C) Prevalence rate D) Incidence rate

A

Mortality rate

328
Q

Which of the following is an example of an emergent disease that has recently become prevalent in the United States?
A) Tuberculosis
B) Lyme disease
C) Smallpox
D) Cholera

A

Lyme disease

329
Q

Which factor is primarily responsible for the emergence of influenza pandemics, occurring every 10 to 40 years?
A) Increased vaccination rates
B) Antigenic shift in the influenza genome
C) Genetic mutation of bacteria
D) Water contamination

A

Antigenic shift in the influenza genome

330
Q

What is a key characteristic that distinguishes reemerging diseases from emergent diseases?
A) Reemerging diseases are always viral infections
B) Reemerging diseases were previously under control but have regained prevalence
C) Reemerging diseases always occur in new geographic areas
D) Reemerging diseases are always caused by bacterial pathogens

A

Reemerging diseases were previously under control but have regained prevalence

331
Q

What is the primary mode of transmission for cholera?
A) Vector-borne through mosquito bites
B) Airborne through respiratory droplets
C) Direct contact with infected bodily fluids
D) Ingestion of contaminated water or food

A

Ingestion of contaminated water or food

332
Q

What is the most likely explanation for the occurrence of reemerging diseases such as tuberculosis?
A) Decreased vaccination coverage
B) Increased antibiotic resistance
C) Improved sanitation and water purification
D) Genetic modification of pathogens for better survival

A

Increased antibiotic resistance

333
Q

Which of the following is a key characteristic of biological weapons used in warfare?
A) They are difficult to produce and deliver
B) They do not affect civilians
C) They are capable of incapacitating or killing individuals in a consistent manner
D) They can only be used for medical purposes

A

They are capable of incapacitating or killing individuals in a consistent manner

334
Q

Which of the following best explains the emergence of the 2009 H1N1 influenza pandemic (swine flu)?
A) A single mutation in a bird flu virus
B) Gene reassortment involving swine, bird, and human influenza viruses
C) The eradication of seasonal influenza vaccines
D) A new bacterial strain spreading rapidly in Europe

A

Gene reassortment involving swine, bird, and human influenza viruses

335
Q

What is a primary factor limiting the long-distance transmission of many respiratory pathogens?
a) High humidity levels
b) Poor survival in air
c) Low temperatures
d) Rapid immune response

A

Poor survival in air

336
Q

Which characteristic differentiates the upper and lower respiratory tracts? a) Air flow
b) Temperature
c) pH levels
d) All of the above

A

All of the above

337
Q

Which pathogen is commonly found in low numbers in the upper respiratory tract of healthy individuals?
a) Mycobacterium tuberculosis
b) Streptococcus pyogenes
c) Bordetella pertussis
d) Chlamydophila pneumoniae

A

Streptococcus pyogenes

338
Q

What is the primary diagnostic method for identifying Streptococcus pyogenes infections? a) Fluorescent antibody staining
b) Culture and beta-hemolysis observation
c) DNA sequencing
d) Immunohistochemistry

A

Culture and beta-hemolysis observation

339
Q

Streptococcus pyogenes is the causative agent of which disease? a) Pertussis
b) Tuberculosis
c) Strep throat

d) Leprosy

A

Strep throat

340
Q

What toxin contributes to the virulence of beta-hemolytic Streptococcus strains?
a) Endotoxin
b) Hemolysin
c) Neurotoxin
d) Lipopolysaccharide

A

Hemolysin

341
Q

Which pathogen causes pertussis (whooping cough)? a) Streptococcus pneumoniae
b) Bordetella pertussis
c) Mycobacterium tuberculosis
d) Mycobacterium leprae

A

Bordetella pertussis

342
Q

What symptom characterizes pertussis? a) Persistent fever
b) Recurrent, violent cough
c) Chest pain
d) Difficulty swallowing

A

Recurrent, violent cough

343
Q

What is the primary method of pertussis prevention? a) Isolation
b) Antibiotics
c) Vaccination
d) Air filtration

A

Vaccination

344
Q

Which pathogen is transmitted via airborne droplets and can cause tuberculosis? a) Mycobacterium tuberculosis
b) Mycobacterium leprae
c) Haemophilus influenzae
d) Streptococcus pneumoniae

A

Mycobacterium tuberculosis

345
Q

What immune mechanism plays a key role in preventing active tuberculosis? a) Antibody-mediated immunity
b) Cell-mediated immunity
c) Complement activation
d) Humoral immunity

A

Cell-mediated immunity

346
Q

Which organism causes leprosy? a) Mycobacterium tuberculosis
b) Mycobacterium leprae
c) Bordetella pertussis
d) Chlamydophila pneumoniae

A

Mycobacterium leprae

347
Q

What is a hallmark of lepromatous leprosy? a) Pulmonary lesions
b) Folded, bulb-like lesions on the body
c) Recurrent high fevers
d) Chronic cough

A

Folded, bulb-like lesions on the body

348
Q

Where are leprosy lesions most likely to form? a) Warmer parts of the body
b) Cooler parts of the body
c) Internal organs
d) The gastrointestinal tract

A

Cooler parts of the body

349
Q

What cells do M. leprae grow in to cause nerve-related symptoms? a) Schwann cells
b) Red blood cells
c) White blood cells
d) Epithelial cells

A

Schwann cells

350
Q

Why are viral infections among the most prevalent in humans? a) Viruses replicate faster than bacteria
b) Viruses can remain infectious in dried mucus for long periods c) Vaccines for viral infections are ineffective
d) Viral infections are always chronic

A

Viruses can remain infectious in dried mucus for long periods

351
Q

What is a common characteristic of most viral diseases? a) Chronic and progressive
b) Acute and self-limiting
c) Always requiring hospitalization
d) Caused by multiple pathogens

A

acute and self-limiting

352
Q

Which of the following has been effectively controlled by vaccination? a) Measles and mumps
b) Smallpox and rabies
c) Chicken pox and rubella

d) Influenza and HIV

A

Measles and mumps

353
Q

What caused the decline in measles cases after the mid-1960s?
a) Better sanitation
b) Antibiotic treatments
c) Widespread immunization programs
d) Natural immunity

A

Widespread immunization programs

354
Q

What is “immune amnesia” caused by the measles virus?
a) Loss of long-term immunity due to age
b) Destruction of memory B cells by the virus
c) Immune system’s inability to recognize viruses
d) Mutation of memory T cells

A

Destruction of memory B cells by the virus

355
Q

Which serious complications can result from measles infections?
a) Meningitis and hepatitis
b) Encephalitis and pneumonia
c) Kidney failure and anemia
d) Chronic fatigue and arthritis

A

Encephalitis and pneumonia

356
Q

What has caused recent increases in measles outbreaks?
a) Antiviral drug resistance
b) Genetic mutations in the virus
c) Populations not immunized or inadequately immunized
d) Increased global travel

A

Populations not immunized or inadequately immunized

357
Q

What type of virus causes rubella?

a) DNA virus from the paramyxovirus family
b) Positive-strand RNA virus of the togavirus group c) Retrovirus from the lentivirus group
d) Negative-strand RNA virus of the filovirus family

A

Positive-strand RNA virus of the togavirus group

358
Q

What is a significant risk of rubella if contracted during the first three months of pregnancy? a) Permanent immune suppression
b) Severe congenital defects in the infant
c) Increased risk of maternal death
d) Chronic respiratory infections in the infant

A

Severe congenital defects in the infant

359
Q

Which symptom is associated with congenital rubella syndrome?
a) High fever
b) Cataracts in the eyes
c) Painful skin rash
d) Enlarged spleen

A

Cataracts in the eyes

360
Q

What is a defining feature of mumps infection? a) Chronic cough
b) Inflammation of the salivary glands
c) Persistent fever
d) Skin lesions

A

Inflammation of the salivary glands

361
Q

Which group was most affected by mumps outbreaks in the United States in 2006, 2016, and 2017?
a) Infants
b) Elderly
c) Young adults (18–34 years old) d) Healthcare workers

A

Young adults (18–34 years old)

362
Q

What was a key recommendation to reduce mumps cases in the United States? a) Mass distribution of antiviral drugs
b) Immunization targeting school-age children and healthcare workers

c) Regular testing for mumps antibodies d) Quarantine of infected individuals

A

Immunization targeting school-age children and healthcare workers

363
Q

What virus causes chicken pox and shingles? a) Varicella-zoster virus (VZV)
b) Paramyxovirus
c) Togavirus
d) Epstein-Barr virus

A

Varicella-zoster virus (VZV)

364
Q

What happens during a shingles outbreak?
a) Chronic coughing develops
b) Nerve cells migrate to skin tissue
c) The virus reactivates and causes painful skin eruptions d) The immune system fails to fight new infections

A

The virus reactivates and causes painful skin eruptions

365
Q

Where does the varicella-zoster virus remain latent? a) Bone marrow
b) Salivary glands
c) Nerve cells
d) Lymph nodes

A

Nerve cells

366
Q

Which virus is the most common cause of the common cold?
a) Coronavirus
b) Rhinovirus
c) Adenovirus
d) Influenza virus

A

Rhinovirus

367
Q

Why is complete protective immunity against the common cold challenging to achieve?
a) Cold viruses do not induce specific immunity
b) The large number of cold pathogens prevents complete protection
c) Antiviral drugs eliminate protective immunity
d) The cold virus mutates annually

A

The large number of cold pathogens prevents complete protection

368
Q

What distinguishes Influenza A viruses from other types of influenza viruses?
a) They contain a positive-sense, single-stranded RNA genome
b) They are segmented DNA viruses
c) They have unique surface glycoproteins, HA and NA
d) They lack a lipid bilayer in their envelope

A

They have unique surface glycoproteins, HA and NA

369
Q

What is the difference between antigenic drift and antigenic shift in influenza viruses?
a) Antigenic drift involves gene mutation; antigenic shift involves gene reassortment
b) Antigenic drift occurs in coronaviruses; antigenic shift occurs in adenoviruses
c) Antigenic drift causes pandemics; antigenic shift causes minor outbreaks
d) Antigenic drift and shift are both caused by environmental factors

A

Antigenic drift involves gene mutation; antigenic shift involves gene reassortment

370
Q

Which influenza strain caused a pandemic in 2009 and is also known as “swine flu”?
a) H5N1
b) H3N2
c) H1N1
d) H7N9

A

H1N1

371
Q

Why should aspirin be avoided in treating influenza, particularly in children?
a) It may lead to antigenic shift
b) It can exacerbate antigenic drift
c) It is ineffective against influenza A
d) It may cause Reye’s Syndrome

A

It may cause Reye’s Syndrome

372
Q

What characteristic distinguishes Staphylococcus species from other bacteria? a) They form spherical spores.
b) They form irregular clumps resembling grape clusters.
c) They are gram-negative, spiral-shaped bacteria.
d) They are strictly anaerobic.

A

They form irregular clumps resembling grape clusters.

373
Q

Which metabolic property allows Staphylococcus species to grow on mannitol salt agar (MSA)?
a) Ability to ferment maltose only
b) Tolerance to salt and ability to ferment mannitol
c) Strict aerobic respiration
d) Fermentation of sucrose exclusively

A

Tolerance to salt and ability to ferment mannitol

374
Q

What is a major virulence factor that protects Staphylococcus aureus from phagocytosis? a) Hemolysin toxin
b) Protein A and coagulase
c) Urease enzyme
d) CagA protein

A

Protein A and coagulase

375
Q

Which Staphylococcus exotoxin is associated with food poisoning? a) TSST-1 (toxic shock syndrome toxin)
b) Hemolysin
c) Enterotoxin

d) Exfoliatin

A

Enterotoxin

376
Q

What type of disease is caused by Staphylococcus aureus producing exfoliatin toxin? a) Toxic shock syndrome
b) Food poisoning
c) Scalded skin syndrome
d) Osteomyelitis

A

Scalded skin syndrome

377
Q

Which enzyme produced by Staphylococcus aureus contributes to tissue invasion? a) Urease
b) Hyaluronidase
c) Catalase
d) CagA

A

Hyaluronidase

378
Q

What type of bacterium is Helicobacter pylori? a) Gram-positive, facultative aerobe
b) Gram-negative, highly motile, spiral-shaped c) Gram-positive, spore-forming, rod-shaped
d) Gram-negative, spherical

A

Gram-negative, highly motile, spiral-shaped

379
Q

Where does Helicobacter pylori typically colonize in the human body? a) Acid-secreting mucosa of the stomach
b) Non-acid-secreting mucosa of the stomach and upper intestine
c) Lymphatic tissue in the intestines
d) Respiratory tract epithelium

A

Non-acid-secreting mucosa of the stomach and upper intestine

380
Q

Which Helicobacter pylori virulence factor promotes duodenal ulcers? a) Catalase
b) DupA
c) Exotoxin A
d) Hemolysin

A

DupA

381
Q

What diagnostic test can confirm the presence of Helicobacter pylori? a) Blood culture
b) Urease breath test for ammonia
c) Gram staining of gastric tissue
d) Catalase activity assay

A

Urease breath test for ammonia

382
Q

Which disease is most strongly linked to Helicobacter pylori colonization? a) Scalded skin syndrome
b) Gastric adenocarcinoma
c) Impetigo
d) Pneumonia

A

Gastric adenocarcinoma

383
Q

How is Helicobacter pylori primarily transmitted?
a) Airborne droplets
b) Person-to-person contact or ingestion of contaminated food or water c) Direct blood exposure
d) Contact with animal reservoirs

A

Person-to-person contact or ingestion of contaminated food or water

384
Q

What is a key characteristic of sexually transmitted infections (STIs)?
a) They are always caused by bacteria
b) They are found only in the gastrointestinal tract
c) Pathogens are generally found in body fluids exchanged during sexual activity
d) They cannot be transmitted through direct contact

A

Pathogens are generally found in body fluids exchanged during sexual activity

385
Q

What distinguishes gonorrhea from syphilis in terms of prevalence and symptoms?
a) Gonorrhea is rare and always symptomatic, while syphilis is common and asymptomatic
b) Gonorrhea is prevalent and often asymptomatic, especially in women, while syphilis has low
prevalence and exhibits obvious symptoms
c) Both are highly prevalent and have similar symptoms d) Syphilis is more common and rarely shows symptoms

A

Gonorrhea is prevalent and often asymptomatic, especially in women, while syphilis has low
prevalence and exhibits obvious symptoms

386
Q

Which bacterium causes gonorrhea? a) Treponema pallidum
b) Chlamydia trachomatis
c) Neisseria gonorrhoeae
d) Herpes simplex virus

A

Neisseria gonorrhoeae

387
Q

What is a common complication of untreated gonorrhea in women? a) Cervical cancer
b) Pelvic inflammatory disease
c) Genital warts
d) Lymphogranuloma venereum

A

Pelvic inflammatory disease

388
Q

What are the stages of syphilis progression? a) Acute, chronic, and latent
b) Primary, secondary, and tertiary
c) Initial, recurring, and chronic
d) Localized, systemic, and congenital

A

Primary, secondary, and tertiary

389
Q

Which STI is the most prevalent bacterial infection worldwide? a) Gonorrhea
b) Syphilis
c) Chlamydia
d) Genital herpes

A

the clap

390
Q

What causes cold sores and fever blisters around the mouth? a) Human papillomavirus (HPV)
b) Herpes simplex virus 1 (HSV-1)
c) Herpes simplex virus 2 (HSV-2)
d) Treponema pallidum

A

Herpes simplex virus 1 (HSV-1)

391
Q

Which STI is primarily associated with the anogenital region? a) Herpes simplex virus 1 (HSV-1)
b) Herpes simplex virus 2 (HSV-2)
c) Chlamydia trachomatis
d) Human papillomavirus (HPV)

A

Herpes simplex virus 2 (HSV-2)

392
Q

What is the relationship between human papillomavirus (HPV) and cervical cancer? a) All HPV infections cause cervical cancer
b) HPV infections may progress to cervical neoplasia, and some lead to cervical cancers c) HPV only causes genital warts, not cancer
d) Cervical cancer is unrelated to HPV infections

A

HPV infections may progress to cervical neoplasia, and some lead to cervical cancers

393
Q
  1. What is the main cause of acquired immunodeficiency syndrome (AIDS)? a) Treponema pallidum
    b) Neisseria gonorrhoeae
    c) Human papillomavirus (HPV)
    d) Human immunodeficiency virus (HIV)
A

HIV

394
Q

Which cell type is progressively depleted in HIV infections? a) CD8+ cytotoxic T cells

b) CD4+ helper T cells
c) B cells
d) Natural killer (NK) cells

A

CD4+ helper T cells

395
Q

Which diagnostic test is used for early detection of HIV infection? a) HIV-EIA antibody test
b) RT-PCR to detect HIV RNA
c) Culture of infected cells
d) Rapid blood glucose test

A

RT-PCR to detect HIV RNA

396
Q

What is a common limitation of antibody-based tests for HIV diagnosis? a) They cannot detect antibodies to HIV
b) They fail to detect infection in individuals who recently acquired HIV
c) They are not specific to HIV
d) They cannot be performed on blood samples

A

They fail to detect infection in individuals who recently acquired HIV

397
Q

Which therapy is used to delay the symptoms of AIDS and prolong life? a) Antibiotics
b) Highly active antiretroviral therapy (HAART)
c) Chemotherapy
d) Vaccination

A

Highly active antiretroviral therapy (HAART)

398
Q

Why is HAART often inaccessible in developing countries? a) It is ineffective against HIV strains in those regions
b) It requires specialized medical equipment
c) It is prohibitively expensive
d) It lacks approval for use in low-income areas

A

It is prohibitively expensive

399
Q

What is the primary focus of epidemiology?
A) Treating diseases in individual patients
B) The occurrence and distribution of health and disease
C) Creating vaccines for all infectious diseases D) None of the above

A

The occurrence and distribution of health and disease

400
Q

What is the goal of identifying the nature of a disease and its transmission? A) To improve hospital infrastructure
B) To develop public health policies
C) To trace and control the spread of diseases
D) Both A and B

A

To trace and control the spread of diseases

401
Q

In developed countries, which of the following is true regarding infectious diseases? A) They cause more deaths than noninfectious diseases
B) They are less of a threat than in developing countries
C) They account for nearly half of all deaths
D) All of the above

A

They are less of a threat than in developing countries

402
Q

What is the term for the total number of new and existing cases of a disease in a population over time?
A) Incidence B) Prevalence C) Mortality D) Morbidity

A

Prevalence

403
Q

What is an epidemic?
A) A disease constantly present at low levels in a population
B) A large number of cases of a disease occurring simultaneously in a population C) A short-term localized disease outbreak
D) A worldwide disease spread

A

A large number of cases of a disease occurring simultaneously in a population

404
Q

What term refers to individuals who are infected but show no or mild symptoms? A) Reservoirs
B) Carriers
C) Hosts
D) None of the above

A

Carriers

405
Q

Which of the following describes a chronic infection?
A) The pathogen quickly overcomes the host, causing death B) The pathogen and host exist in a balanced relationship C) The disease lasts only a few days
D) All of the above

A

The pathogen and host exist in a balanced relationship

406
Q

Which of the following is not part of the stages of disease progression? A) Incubation period
B) Decline period
C) Herd immunity period
D) Convalescent period

A

Herd immunity period

407
Q

What is the meaning of morbidity in epidemiology? A) Incidence of death in a population
B) Incidence of disease, both fatal and nonfatal
C) The number of new disease cases over time
D) The number of immune individuals in a population

A

Incidence of disease, both fatal and nonfatal

408
Q

Disability-Adjusted Life Year (DALY) measures disease burden in terms of: A) Years lost due to disease
B) Disability caused by disease
C) Premature death
D) All of the above

A

All of the above

409
Q

What happens to the virulence of a pathogen during host-to-host transmission over time? A) It increases significantly
B) It diminishes as the host develops resistance
C) It remains unchanged
D) None of the above

A

It diminishes as the host develops resistance

410
Q

Which condition could lead to a pathogen remaining highly virulent? A) Effective herd immunity
B) Host-to-host transmission
C) Non-reliance on host-to-host transmission D) Both A and B

A

Non-reliance on host-to-host transmission

411
Q

Herd immunity protects a population by:
A) Preventing the pathogen from being passed on B) Ensuring all individuals are vaccinated
C) Eliminating the pathogen entirely
D) Reducing the prevalence of all diseases

A

Preventing the pathogen from being passed on

412
Q

What is a characteristic of diseases like influenza?
A) They occur in cycles
B) They rarely spread person-to-person C) They are always endemic
D) They are unaffected by herd immunity

A

They occur in cycles

413
Q

Which of the following is true regarding the coevolution of a host and its pathogen? A) A highly virulent pathogen will always spread rapidly
B) Pathogens killing hosts too quickly may become extinct
C) Virulence always increases over time
D) None of the above

A

Pathogens killing hosts too quickly may become extinct

414
Q

What is the leading cause of death among infectious diseases? A) Tuberculosis
B) Diarrheal diseases
C) Lower respiratory tract infections
D) Malaria

A

Tuberculosis

415
Q
  1. Which of the following diseases is categorized as a lower respiratory tract infection? A) COVID-19
    B) Cholera
    C) Tuberculosis
    D) All of the above
A

COVID

416
Q

What is the second leading cause of death among infectious diseases? A) Diarrheal diseases
B) Malaria
C) AIDS
D) Tuberculosis

A

Diarrheal diseases

417
Q

Which pathogens are significant contributors to diarrheal diseases? A) Cholera and Rotavirus
B) Shigella and certain E. coli strains
C) Cryptosporidium
D) All of the above

A

) All of the above

418
Q

Which of the following is a protozoan associated with diarrheal diseases? A) Cholera
B) Cryptosporidium
C) Rotavirus
D) Shigella

A

Cryptosporidium

419
Q

What is the third leading infectious disease killer globally? A) Malaria
B) AIDS
C) Tuberculosis
D) Diarrheal diseases

A

Tuberculosis

420
Q

Among infectious diseases, what comes after Tuberculosis in terms of global mortality? A) Lower respiratory tract infections
B) AIDS
C) Diarrheal diseases
D) Malaria

A

AIDS

421
Q

Which of the following statements about malaria is true? A) Its global mortality rate is 10%
B) 90% of deaths occur in children under 5 years old C) It is caused by a bacterium
D) None of the above

A

90% of deaths

422
Q

What percentage of malaria-related deaths occur in children under the age of five? A) 50%
B) 70% C) 90% D) 100%

A

90%

423
Q

Which of the following diseases has the lowest mortality rate globally but still significantly impacts children?
A) Malaria
B) Tuberculosis C) Cholera
D) AIDS

A

Malaria

424
Q

Which of these diseases includes significant contributions from bacterial pathogens? A) Malaria and AIDS
B) Tuberculosis and Shigella
C) COVID-19 and Rotavirus
D) All of the above

A

aTuberculosis and Shigella

425
Q

Which of the following lists ranks infectious diseases in order of their mortality rates, starting with the highest?
A) Tuberculosis > Malaria > Diarrheal diseases
B) Lower respiratory tract infections > Diarrheal diseases > Tuberculosis C) AIDS > Tuberculosis > Diarrheal diseases
D) None of the above

A

Lower respiratory tract infections > Diarrheal diseases > Tuberculosis

426
Q

Which of the following is not a diarrheal disease? A) Cholera
B) Rotavirus
C) Malaria
D) Shigella

A

malaria

427
Q

Which of these infectious diseases is caused by a virus? A) Cryptosporidium
B) Rotavirus
C) Cholera
D) Shigella

A

rotavirus

428
Q

Which of the following diseases has protozoan origins? A) Tuberculosis
B) Malaria and Cryptosporidium
C) AIDS
D) Cholera

A

malaria and Cryptosporidium

429
Q

What is a typical outcome of host-to-host coevolution?
A) The parasite becomes more virulent
B) The parasite becomes extinct
C) The host becomes more resistant, and the parasite’s virulence diminishes D) The parasite relies more on non-host reservoirs

A

The host becomes more resistant, and the parasite’s virulence diminishes

430
Q

The host becomes more resistant, and the parasite’s virulence diminishes

A

It kills its host before transmission

431
Q

What type of pathogen transmission involves living or nonliving intermediaries? A) Direct transmission
B) Indirect transmission
C) Zoonotic transmission
D) Airborne transmission

A

indirect transmission

432
Q

Which of the following is a living agent of indirect transmission? A) Soil
B) Vector
C) Fomite
D) Air

A

vector

433
Q

What is an example of a zoonotic disease? A) Influenza
B) Cholera
C) Rabies
D) None of the above

A

rabies

434
Q

Typhoid Mary is an example of: A) A vector
B) A common-source epidemic C) A carrier
D) A zoonotic reservoir

A

carrier

435
Q

hich of the following has the highest basic reproduction number? A) Influenza
B) Measles
C) Rubella
D) Polio

A

measles

436
Q

Which disease control strategy involves restricting the movement of infected individuals? A) Surveillance
B) Immunization
C) Quarantine

D) Eradication

A

quarantine

437
Q

How are airborne pathogens typically controlled? A) Quarantine of infected individuals
B) Water purification systems
C) They are difficult to control effectively
D) Immunization of the host

A

They are difficult to control effectively

438
Q

What is the goal of pathogen eradication? A) Eliminate a pathogen from living hosts only B) Remove all pathogens from reservoirs
C) Reduce the pathogen’s virulence
D) Control the host population

A

Remove all pathogens from reservoirs

439
Q

Which of these diseases has been eradicated through immunization? A) Polio
B) Smallpox
C) Rabies
D) Measles

A

smallpox

440
Q

What is a significant difference between infectious disease patterns in Africa and the Americas?

A) Noninfectious diseases dominate mortality in Africa
B) Infectious disease death rates are higher in the Americas C) Infectious diseases cause most deaths in Africa
D) Travelers to Africa are not at risk for infection

A

Infectious diseases cause most deaths in Africa

441
Q

Which of the following diseases is considered one of the least transmissible? A) Influenza
B) Measles
C) Pertussis
D) Polio

A

influenza

442
Q

What are diseases that suddenly become prevalent called? A) Epidemic diseases
B) Endemic diseases
C) Emergent diseases
D) Reemerging diseases

A

Emergent diseases

443
Q

Reemerging diseases are defined as:
A) Diseases that have become prevalent after being under control B) Diseases that were eradicated but have reappeared globally

C) Newly discovered diseases with high mortality rates D) Diseases restricted to developing countries

A

Diseases that have become prevalent after being under control

444
Q

Which of the following is an emergent disease in the United States? A) Polio
B) Lyme disease
C) Malaria
D) Tuberculosis

A

Lyme

445
Q

What is the vector for Lyme disease? A) Mosquitoes
B) Ticks
C) Fleas
D) Rodents

A

Ticks

446
Q

Which disease is caused by Vibrio cholerae? A) AIDS
B) Cholera
C) Influenza
D) Hemorrhagic fever

A

cholera

447
Q

How is cholera primarily transmitted?

A) Aerosol spray
B) Direct host-to-host contact
C) Ingestion of contaminated water D) Vector-borne transmission

A

Ingestion of contaminated water

448
Q

What characteristic differentiates antigenic shift from antigenic drift in influenza viruses? A) Antigenic shift involves gene reassortment, while antigenic drift involves gene mutation B) Antigenic drift causes pandemics, while antigenic shift causes localized outbreaks
C) Antigenic shift is a minor change, while antigenic drift is a major change
D) Antigenic drift occurs every 10 years, while antigenic shift is constant

A

Antigenic shift involves gene reassortment, while antigenic drift involves gene mutation

449
Q
  1. What type of influenza was responsible for the 2009 pandemic? A) Avian influenza
    B) Swine influenza (H1N1)
    C) Human influenza (H3N2)
    D) Reassorted bird-human influenza
A

swine

450
Q

Which of the following is a characteristic of an effective biological weapon? A) Complex to produce and deliver
B) Debilitates but does not kill
C) Safe for offensive personnel to use
D) Difficult to spread consistently

A

C) Safe for offensive personnel to use

451
Q

Which bacterial toxin is considered a potential biological weapon? A) Cholera toxin
B) Botulinum toxin
C) Tetanus toxin
D) Diphtheria toxin

A

botulinum

452
Q

Why is the smallpox virus considered a potential biological weapon? A) It has a low mortality rate but is hard to control
B) It can be spread by aerosol and contact, causing a high mortality rate C) Vaccines are widely available and used by the general population
D) It is challenging to deliver consistently

A

It can be spread by aerosol and contact, causing a high mortality rate

453
Q

How was the 2009 H1N1 swine flu pandemic an example of reassortment?
A) It was caused by gene mutation in a single influenza strain
B) It resulted from simultaneous infections with swine, bird, and human influenza strains C) It emerged from a shift in human behavior and agricultural practices
D) It was a result of antigenic drift over several decades

A

It resulted from simultaneous infections with swine, bird, and human influenza strains

454
Q

Which disease is transmitted via a small water crustacean as part of its cycle? A) Cholera
B) Influenza

C) Tuberculosis D) Zika virus

A

Zika virus

455
Q

What is the estimated mortality rate of smallpox in unvaccinated populations? A) 10%
B) 20%
C) 30% or more
D) 50%

A

30%

456
Q

Why is the potential deployment of smallpox as a biological weapon considered low? A) It is no longer infectious in nature
B) Military personnel are routinely vaccinated against smallpox
C) The vaccine has not been developed for civilian use
D) Smallpox virus cannot be easily spread

A

Military personnel are routinely vaccinated against smallpox