Unit 5: Bacterial Cell Structure & Mycology & Unit 6: Parasitology & Virology Flashcards

1
Q

What is the function of collagenase in pathogens?

A

Collagenase breaks down collagen, facilitating the spread of pathogens.

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2
Q

How does hyaluronidase assist in pathogen penetration?

A

Hyaluronidase degrades hyaluronic acid, allowing easier tissue penetration for pathogens.

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3
Q

What role does coagulase play in bacterial evasion of the immune system?

A

Coagulase causes blood to clot, helping pathogens evade the immune response.

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4
Q

What is mutualism in host-microbe relationships?

A

A relationship where both organisms benefit, like E. coli providing Vitamin K to humans.

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5
Q

What are the key characteristics of exotoxins?

A

Exotoxins are protein-based, heat labile, and released by both Gram-positive and Gram-negative bacteria.

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6
Q

What distinguishes commensalism from mutualism?

A

In commensalism, one organism benefits while the other is neither helped nor harmed.

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7
Q

How is parasitism defined in host-microbe interactions?

A

It’s a relationship where one organism benefits at the expense of another, such as disease-causing bacteria.

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8
Q

What is the difference between infection and infestation?

A

Infection involves parasitic organisms multiplying in a host, while infestation refers to larger organisms like lice.

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9
Q

What is an endotoxin and where is it found?

A

Endotoxin is lipopolysaccharide (LPS), present only in Gram-negative bacteria.

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10
Q

What are the key steps involved in the infectious disease process?

A

Entry and attachment, damage, escape, and the role of virulence factors.

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11
Q

What is pathogenicity?

A

Pathogenicity is the ability of a pathogen to cause disease, varying among different pathogens.

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12
Q

What role do virulence factors play in bacterial infections?

A

They enhance a bacterium’s ability to cause disease, including structures like fimbriae and toxins.

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13
Q

How do bacteria evade host defenses during infection?

A

By defending against immune responses, attacking host cells, hiding from detection, and using capsules.

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14
Q

What are inherited diseases caused by?

A

Inherited diseases are caused by a faulty gene.

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15
Q

What distinguishes congenital diseases from other disease types?

A

Congenital diseases result from damage during development.

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16
Q

What types of damage can bacteria cause during an infection?

A

Bacteria can cause damage through enzyme release, toxin release, and overstimulation of the immune response.

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17
Q

How do invasive bacteria cause disease?

A

Invasive bacteria spread through tissues using digestive enzymes that damage tissues.

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18
Q

What are adhesins and their role in bacterial attachment?

A

Adhesins are molecules that facilitate the attachment of bacteria to host tissues.

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19
Q

What are communicable diseases?

A

Communicable diseases can be spread from one person to another.

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20
Q

What is the largest organ in the body and its role in microbial colonization?

A

The skin is the largest organ, colonized by various microorganisms with factors that regulate their populations.

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21
Q

What mechanisms do viruses employ to cause disease?

A

Viruses multiply inside host cells, leading to cell death and altering cell cycle regulation.

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22
Q

Where are bacteria most densely populated in the gastrointestinal tract?

A

The mouth has the highest density of bacteria, while numbers increase significantly towards the end of the small intestine.

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23
Q

What factors influence the risk of contracting infectious diseases?

A

Infectious disease risk is influenced by the number of infecting organisms, virulence, and host factors like health and immune status.

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24
Q

What distinguishes opportunistic pathogens from regular pathogens?

A

Opportunistic pathogens cause disease in weakened hosts or atypical body locations, unlike primary pathogens which affect healthy individuals.

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25
Q

What are saprotrophs and their ecological function?

A

Saprotrophs decompose dead organic matter, playing a key role in nutrient cycling within ecosystems.

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26
Q

What are superantigens and their role in immune response?

A

Superantigens bind MHC class II and T-cell receptors, causing excessive cytokine release from T helper cells.

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27
Q

How do superantigens activate T-cells?

A

Superantigens activate T-cells regardless of peptide recognition, triggering proliferation and cytokine release.

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28
Q

What is the incubation period in infectious disease?

A

The incubation period is the time between infection and symptom onset.

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29
Q

How do pathogens breach mucosal barriers?

A

Pathogens exploit antigen-sampling processes, using M cells and MALT to penetrate mucous membranes.

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30
Q

What characterizes an acute illness?

A

Acute illness has a short duration where the pathogen is eliminated by host defenses.

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31
Q

What is the effect of Toxic Shock Syndrome Toxin (TSST)?

A

TSST is a superantigen that induces toxic shock via massive cytokine release.

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32
Q

What role do dermatophytes play in fungal pathogenesis?

A

Dermatophytes cause superficial infections of hair, skin, and nails by degrading keratin using keratinase enzymes.

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33
Q

What role do adhesins play in infection establishment?

A

Adhesins attach to host cell receptors, often located on pili, facilitating bacterial adherence.

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34
Q

How do viruses attach to host cells?

A

Viruses utilize specific receptors on host cells to attach and initiate infection.

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35
Q

Define latent illness.

A

Latent illness may recur if host immunity weakens, without causing symptoms.

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36
Q

What is Exfoliatin and its impact on the skin?

A

Exfoliatin destroys skin binding material, leading to scalded skin syndrome.

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37
Q

How can normal microbiota like Candida albicans lead to disease?

A

Candida albicans can cause disease in immunocompromised hosts despite being part of the normal microbiota.

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38
Q

What strategies does Shigella use to survive within the host?

A

Shigella survives phagocytosis, induces apoptosis, and utilizes actin polymerization to spread between epithelial cells.

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39
Q

What role do hydrolytic enzymes play in bacterial infection?

A

Hydrolytic enzymes break down connective tissue, aiding tissue destruction and bacterial spread.

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40
Q

What factors influence the incubation period?

A

Factors include pathogen growth rate, host condition, and infectious dose received.

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41
Q

What mechanisms do viruses use to evade immune responses?

A

Viruses block host gene expression, inhibit antiviral enzymes, and modify surface antigens.

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42
Q

How do bacteria evade secretory IgA during colonization?

A

Bacteria evade secretory IgA through rapid pili turnover, antigenic variations, and IgA protease production.

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43
Q

What is a characteristic feature of dimorphic fungi?

A

Dimorphic fungi exist as molds in the environment and develop into yeast forms in the lungs after inhalation.

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44
Q

How does Mycobacterium tuberculosis invade host cells?

A

Mycobacterium tuberculosis invades through alveolar macrophages, using surface proteins to avoid activation.

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45
Q

What are A-B toxins composed of?

A

A-B toxins consist of an A subunit, which is toxic, and a B subunit, which binds to the host cell.

46
Q

How do chronic infections differ from acute infections?

A

Chronic infections develop slowly and last for months or years, unlike acute infections.

47
Q

What strategies do pathogens use to avoid destruction by phagocytes?

A

Pathogens employ various means, including altering surface antigens and mimicking host molecules.

48
Q

What defines a localized infection?

A

An infection limited to a small area, e.g., a boil from Staphylococcus aureus.

49
Q

What role does normal microbiota play in protecting against pathogens?

A

Normal microbiota prevent pathogen attachment, compete for nutrients, and produce antimicrobial compounds.

50
Q

How do some viruses evade antibody detection?

A

By moving cell-to-cell, inducing syncytium, and using antibodies for uptake by macrophages.

51
Q

What is the function of the Type III Secretion System?

A

The Type III Secretion System delivers effector proteins to host cells, altering cytoskeletal structures and inducing uptake.

52
Q

What strategies do protozoa and helminths use to evade the immune system?

A

They employ intracellular survival, antigen variation, and coating with host proteins to avoid immune detection.

53
Q

What role do skin and mucous membranes play in microbial ecosystems?

A

They serve as barriers to pathogens and host complex ecosystems of microorganisms.

54
Q

Why do some pathogens reside within host cells?

A

Pathogens avoid complement proteins, phagocytes, and antibodies by hiding in host cells.

55
Q

What is septicemia?

A

An acute, life-threatening illness caused by infectious agents or their products in the bloodstream.

56
Q

How do pathogens commonly breach mucous membranes?

A

Pathogens penetrate mucous membranes, a frequent entry point for various infections.

57
Q

What types of damage do protozoan and helminth pathogens cause to the host?

A

Damage can result from nutrient consumption, intestinal blockage, harmful enzyme production, and immune response-induced tissue damage.

58
Q

What ancient belief about diseases was common before scientific understanding?

A

Diseases were often viewed as divine punishment.

59
Q

How do pathogens like Neisseria gonorrhoeae evade antibodies?

A

They produce IgA protease that cleaves IgA and use antigenic variation to change surface antigens.

60
Q

What are the limitations of Koch’s postulates in establishing infectious disease causation?

A

Limitations include organisms that can’t be cultured, asymptomatic infections, polymicrobial diseases, and lack of suitable animal models.

61
Q

What role does the protein p53 play in viral infections?

A

Viruses can prevent or delay apoptosis by controlling the regulatory protein p53.

62
Q

What are Koch’s Postulates?

A

Criteria to determine the causative agent of infectious diseases, established by Robert Koch.

63
Q

How do capsules help pathogens avoid phagocytosis?

A

Capsules interfere with opsonization and bind proteins that inactivate C3b.

64
Q

How can antibiotic treatment disrupt normal microbiota?

A

Antibiotics can kill beneficial bacteria, allowing pathogens like Candida albicans and Clostridium difficile to overgrow.

65
Q

What is an example of mutualism in the human microbiota?

A

Bacteria in the large intestine synthesize vitamins while receiving warmth and energy from the host.

66
Q

How do A-B toxins enter host cells?

A

The B subunit binds to a host cell molecule, and the toxin is internalized via endocytosis.

67
Q

What are Molecular Koch’s postulates related to virulence factors?

A

They state virulence factors should exist in pathogenic strains, disrupting them reduces virulence, and restoring them reinstates virulence.

68
Q

What example illustrates how bacteria penetrate the skin?

A

Staphylococcus aureus enters through cuts or wounds, showcasing bacteria’s reliance on injuries for skin penetration.

69
Q

Who proposed that communicable diseases were caused by living agents?

A

Fracastorius in 1546 suggested living agents caused communicable diseases.

70
Q

What are direct effects of pathogens on hosts?

A

Direct effects result from toxins produced by pathogens affecting host tissue directly.

71
Q

What indicates the presence of substances in the blood?

A

The suffix -emia, used in terms like bacteremia and viremia.

72
Q

How do pathogens produce toxins in the context of infectious diseases?

A

Pathogens can either produce toxins that are ingested or colonize mucous membranes to produce toxins.

73
Q

How do viruses manipulate MHC class I presentation?

A

They block MHC class I molecules or present counterfeit versions, evading T cell and NK cell detection.

74
Q

How do resident and transient microbiota differ?

A

Resident microbiota inhabit specific sites for extended periods while transient microbiota temporarily inhabit the body.

75
Q

What is the difference between colonization and infection?

A

Colonization is microbe establishment on surfaces, while infection involves the presence of a pathogen causing health impairment.

76
Q

What important theory did Robert Koch establish in 1876?

A

Koch provided proof for the germ theory of disease.

77
Q

What mechanisms do pathogens use to avoid phagocyte destruction?

A

Pathogens evade phagocyte destruction by using strategies like C5a degradation and membrane-damaging toxins.

78
Q

What role does M protein play in pathogen evasion?

A

M protein binds regulatory proteins that inactivate C3b in Streptococcus pyogenes.

79
Q

What is bacteremia?

A

The presence of bacteria circulating in the blood, which can be transient.

80
Q

What is the significance of tissue invasion in pathogen-caused diseases?

A

Tissue invasion allows pathogens to evade host defenses, enhancing their ability to cause disease.

81
Q

What are exotoxins and how do they work?

A

Exotoxins are proteins that can damage hosts, acting locally or systemically, and provoking immune responses.

82
Q

What is normal microbiota and its significance?

A

Normal microbiota are beneficial microbes that balance human health but can cause disease opportunistically.

83
Q

How do pathogens and hosts evolve together in infectious diseases?

A

They typically evolve towards a balanced pathogenicity, illustrated by interactions like the myxoma virus with rabbits.

84
Q

How does C5a peptidase function in avoiding immune response?

A

C5a peptidase degrades C5a, reducing phagocyte recruitment to infection sites.

85
Q

What is the significance of mucosal-associated lymphoid tissue (MALT) in immune response?

A

MALT development is crucial for a robust immune response, enhanced by exposure to normal microbiota.

86
Q

What distinguishes primary pathogens from opportunistic pathogens?

A

Primary pathogens cause disease in healthy individuals, while opportunistic pathogens affect compromised hosts or unusual sites.

87
Q

How do Fc receptors contribute to pathogen survival?

A

Fc receptors bind the Fc region of antibodies, hindering phagocyte recognition and attachment.

88
Q

What is the role of hemolysins in exotoxins?

A

Hemolysins lyse red blood cells, causing cell lysis.

89
Q

What is the role of toxoids in vaccination against toxins?

A

Toxoids are inactivated toxins used in vaccines to help induce immunity against harmful exotoxins.

90
Q

What factors increase susceptibility to infections in immunocompromised individuals?

A

Factors include malnutrition, cancer, AIDS, surgery, genetic defects, and immunosuppressive therapy.

91
Q

What role do capsules play in bacterial evasion of phagocytes?

A

Capsules inhibit phagocyte recognition and attachment, making bacteria harder to target.

92
Q

What does the hygiene hypothesis suggest about microbial exposure?

A

Insufficient microbial exposure can increase allergy susceptibility, emphasizing the importance of normal microbiota.

93
Q

Why are normal microbiota important for human health?

A

They are crucial for metabolic processes and immune system function.

94
Q

How does Neisseria gonorrhoeae evade the complement system?

A

Neisseria gonorrhoeae binds complement regulatory proteins, preventing the activation of the membrane attack comple

95
Q

Define virulence and its significance in infectious disease.

A

Virulence indicates the degree of pathogenicity of a microorganism, essential for understanding disease severity.

96
Q

What mechanisms do some pathogens use to survive inside phagocytes?

A

Pathogens escape into the cytoplasm or prevent phagosome-lysosome fusion.

97
Q

How do pathogens survive within phagocytes?

A

Pathogens escape phagosomes, prevent phagosome-lysosome fusion, or adapt to survive harsh environments.

98
Q

What is a common example of a phospholipase toxin?

A

Clostridium perfringens produces a phospholipase toxin associated with gas gangrene.

99
Q

How does the composition of normal microbiota change over time?

A

Microbiota composition is dynamic, influenced by host physiology, diet, and environmental factors.

100
Q

What is an infectious dose (ID50)?

A

ID50 indicates the number of microbes needed to infect 50% of a population, showing pathogen survival capabilities.

101
Q

Which microorganisms are commonly found in the large intestine?

A

Bacteroides, Escherichia, Proteus, Klebsiella, Lactobacillus, Streptococcus, Candida, Clostridium, Pseudomonas, and Enterococcus.

102
Q

What are the key components involved in phagocytosis?

A

Key components include phagocytes, phagosomes, phagolysosomes, and digestive enzymes.

103
Q

What is endotoxin composed of and what triggers an inflammatory response?

A

Endotoxin is composed of lipopolysaccharide (LPS); Lipid A triggers an inflammatory response.

104
Q

How do symptoms differ from signs in infectious diseases?

A

Symptoms are subjective patient experiences, while signs are objective evidence observed by healthcare providers.

105
Q

How can A-B toxins be used therapeutically?

A

Their structure allows for innovative vaccine development and targeted delivery of beneficial compounds.

106
Q

Which pathogen is known for surviving the phagolysosome’s harsh environment?

A

Coxiella burnetii survives by delaying phagolysosome fusion.

107
Q

How do endotoxins affect the immune system?

A

Endotoxins induce phagocytosis, MAC formation, and activate both innate and adaptive defenses.

108
Q

What is the main difference between exotoxins and endotoxins?

A

Exotoxins are proteins from both Gram-positive and Gram-negative bacteria; endotoxins are only from Gram-negative bacteria and consist of Lipid A.

109
Q

What damaging effects can inflammation have on host tissues?

A

Phagocytic cells may release enzymes and toxic products, causing tissue damage.

110
Q

What consequences can arise from immune complexes formed by antigen-antibody reactions?

A

They can settle in kidneys and joints, activate the complement system, and lead to inflammation.