Introduction To Microbiology Flashcards

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1
Q

Who founded microscopes and is called the founder of microbiology

A

Antonie Van Leeuwenhoek

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2
Q

Who coined the germ theory and is the father of modern microbiology and found the vaccine against anthrax in animals

A

Louis Pasteur

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3
Q

Who is the father of immunology

A

Edward Jenner

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4
Q

Who is the founder of modern bacteriology , discovered Bacillus anthracis (Anthrax bacillus), Mycobacterium tuberculosis, and Vibrio cholerae. And modified Ziehl-Neelsen Acid Fast staining procedure which was introduced by Ehrlich. And is considered the father of medical microbiology
He also realized that microorganisms cause diseases

A

Robert Koch

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5
Q

Who founded penicillin(Penicillium notatum )which acts on Gram positive bacteria

A

Alexander Fleming

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6
Q

Who discovered hand hygiene( hand washing)

A

Ignaz Semmelweis

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7
Q

What are Koch’s postulates

A
  1. If a person A has a disease, the pathogen that caused the disease should be the same pathogen that caused the same disease in person B and that pathogen wil not be found in healthy people or the pathogen must be present in every case of the disease
    ExMple if person A has fever and chills and it’s cAused by twisty germ, person B also having fever and chills , the disease should also be twisty germ
  2. The pathogen should be isolated from the diseased host Nd grown in a pure culture to make sure that apart from the pathogen, no other microorganism grows or will be present
    in the culture
  3. When the pathogen (grown from the pure culture )that caused person B’s sickness is put
    In a healthy susceptible person, the healthy person should show the same symptoms Person B is showing or the same disease must be reproduced
  4. The pathogen inoculated ( introduced ) into the experimentally infected host( who was once healthy) should be recoverable
    These postulates show whether a particular disease is caused by a particular pathogen
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8
Q

Limitations of Koch’s postulates

A
  1. not all pathogens inoculated into an experimentally infected person cause the person to produce symptoms.
  2. Pathogens can also be found in healthy individuals. Eg. H pylori is part of the bacteria normally found in the stomach and it also causes chronic gastritis. People can be healthy and still have the H pylori in their stomach. They also will not have chronic gastritis
  3. Not all bacteria can be cultured in a pure culture. Example, the bacteria that causes leprosy( Mycobacterium leprae )
  4. Not all human pathogens can be replicated in an animal host. ExMple viruses
  5. Not all people are susceptible to certain diseases thus they will not show any symptoms when the pathogen is introduced into their body.
  6. Not all people will show the exact same symptoms - limitations for postulate 3
  7. Those who show the same symptoms doesn’t necessarily mean that their diseases are caused by the same pathogen
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9
Q

Importance of capsules , cell wall,ribosomes , pili(fimbriae) flagella in bacteria

A

capsules play a number of roles, but the most important are to keep the bacterium from drying out and to protect it from phagocytosis (engulfing) by larger microorganisms. The capsule is a major virulence factor( Virulence factors are molecules produced by bacteria, viruses, fungi, and protozoa that add to their effectiveness and enable them to achieve their goal) In the major disease-causing bacteria

Cell wall- protects the cell from the environment and prevents the cell from bursting

Cytoplasmic membranes - a barrier that allows them to selectively interact with their environment. Membranes are also dynamic, constantly adapting to different conditions.

Flagella- The flagella beat in a propeller-like motion to help the bacterium move toward nutrients; away from toxic chemicals;

Pili (singular -pilus) Many species of bacteria have pili (singular, pilus), small hairlike projections emerging from the outside cell surface. These outgrowths assist the bacteria in attaching to other cells and surfaces, such as teeth, intestines, and rocks. Without pili, many disease-causing bacteria lose their ability to infect because they’re unable to attach to host tissue

Ribosomes-There are sufficient differences between bacterial ribosomes and eukaryotic ribosomes that some antibiotics will inhibit the functioning of bacterial ribosomes, but not a eukaryote’s, thus killing bacteria but not the eukaryotic organisms they are infecting.

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10
Q

Most antibiotics target which part of the bacteria cell

A

The cell wall

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11
Q

WhT are the Bacteria classification with respect to cell wall and who brought about the staining technique?

A

Gram positive - have thick peptidoglycan layer. ( this is the virulent factor for the gram positive)After staining it appears purple or violet
Gram negative- bunch lipopolysaccharides(endotoxins) but small peptidoglycan layer( this is the virulent factor for gram negative)
Gram negative is more toxic and easily leads to sepsis . After the stain, it appears pink

Hans Christian Joachim GRAM, Gram stain, still a standard technique to classify bacteria and make them more visible under a microscope.

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12
Q

Stains for Gram staining and why gram positive stains but gram negative doesn’t

A

Crystal violet
Methylene blue

Gram positive bacteria stain violet due to the presence of a thick layer of peptidoglycan in their cell walls, which retains the crystal violet these cells are stained with. Alternatively, Gram negative bacteria stain pink cuz it does not retain the crystal violet during the decoloring process.

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13
Q

Process of Gram Staining

A

Cells are stained with crystal violet dye. Next, a Gram’s iodine solution (iodine and potassium iodide) is added to form a complex between the crystal violet and iodine. This complex is a larger molecule than the original crystal violet stain and iodine and is insoluble in water.

decolorizer such as ethyl alcohol or acetone is added to the sample, which dehydrates the peptidoglycan layer, shrinking and tightening it. The large crystal violet-iodine complex is not able to penetrate this tightened peptidoglycan layer, and is thus trapped in the cell in Gram positive bacteria. Conversely, the the outer membrane of Gram negative bacteria is degraded and the thinner peptidoglycan layer of Gram negative cells is unable to retain the crystal violet-iodine complex and the color is lost.

A counterstain, such as the weakly water soluble safranin, is added to the sample, staining it red. Since the safranin is lighter than crystal violet, it does not disrupt the purple coloration in Gram positive cells. However, the decolorized Gram negative cells are stained red.

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14
Q

Reagents for Gram staining

A

Primary stain (crystal violet), Mordant (iodine), Decolorizer (ethanol or acid-alcohol) and Counter stain (safranin or dilute carbol-fuchsin).

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15
Q

Why doesn’t the Gram stain apply to some bacteria

A

Some bacteria produce the waxy substance mycolic acid when they construct their cell walls. Mycolic acid acts as a barrier, protecting the cells from dehydrating, as well as from phagocytosis by immune system cells in a host. This waxy barrier also prevents stains from penetrating the cell, which is why the Gram stain does not work with mycobacteria such as Mycobacterium, which are pathogens of humans and animals.

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16
Q

Principles of acid fast staining

A

When the smear is stained with carbol fuchsin, it solubilizes the lipoidal material present in the Mycobacterial cell wall but by the application of heat, carbol fuchsin further penetrates through lipoidal wall and enters into cytoplasm. Then after all cell appears red. Then the smear is decolorized with decolorizing agent (3% HCL in 95% alcohol) but the acid fast cells are resistant due to the presence of large amount of lipoidal material in their cell wall which prevents the penetration of decolorizing solution. The non-acid fast organism lack the lipoidal material in their cell wall due to which they are easily decolorized, leaving the cells colorless. Then the smear is stained with counterstain, methylene blue. Only decolorized cells absorb the counter stain and take its color and appears blue while acid-fast cells retain the red color.

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17
Q

Acid fast stains acid fast organisms what color and non acid fast organisms what color
And give examples of acid fast organisms and non acid fast organisms

A

Acid fast: Bright red to intensive purple (B), Red, straight or slightly
curved rods, occurring singly or in small groups, may appear beaded
Non-acid fast: Blue color (A)

Acid-fast: Mycobacterium tuberculosis
Non acid fast- Escherichia coli ( also gram negative)

18
Q

WhT is termed as Acid fastness

A

Acid fastness is a physical property that gives a bacterium the ability to resist decolorization by acids during staining procedures.

19
Q

Reagents for acid fast staining

A

Primary dye -Carbolfuchsin
Decolorizer Acid-alcohol
Counterstain-Methylene blue

20
Q

Who founded the acid fast staining

A

Ziehl Neelsen

21
Q

Bacteria can acquire more virulent factors true or false

A

True

22
Q

Other was of classifying bacteria

A

If they are rod shaped- Bacilli
Or round- Cocci
Or spiral- Spirilla

Arrangement- in chains or in clusters or in groups of twos or in groups of fours

23
Q

Definition of beta haemolysis and alpha haemolysis as a way to distinguish between bacteria.

A

https://microdok.com/wp-content/uploads/2018/09/haemolysis-on-BA.png

With beta haemolysis- the organisms eats up the blood cells so around it looks transparent

Alpha haemolysis- the organisms eat some of the blood cells partially so around it looks translucent
For more clarification, find pics of it

24
Q

E coli is beta haemolytic true or false

A

True

25
Q

Story of hand washing

A

Ignaz Semmelweis, a Hungarian doctor working in Vienna General Hospital, is known as the father of hand hygiene. In 1846, he noticed that the women giving birth in the medical student/doctor-run maternity ward in his hospital were much more likely to develop a fever and die compared to the women giving birth in the adjacent midwife-run maternity ward. He decided to investigate, seeking differences between the two wards. He noticed that doctors and medical students often visited the maternity ward directly after performing an autopsy. Based on this observation, he developed a theory that those performing autopsies got ‘cadaverous particles’ on their hands, which they then carried from the autopsy room into the maternity ward. Midwives did not conduct surgery or autopsies, so they were not exposed to these particles.

26
Q

John Snow story

A

late August of 1853, cholera broke out in the Broad Street area, and the residents panicked and many began to flee. A hand pump was located right on Broad Street, and Snow was immediately suspicious. Water samples did not reveal gross contamination, but Snow persisted and began to collect detailed information on where the victims had gotten their drinking water. He obtained the names and the addresses of the first 83 victims who had died by the end of the first week. He went to their homes and learned from relatives that the vast majority of them had obtained their water from the Broad St. pump.

On Sept. 6 Snow appeared at the meeting of the local Board of Guardians and presented his evidence that the pump was the source of the outbreak. He argued that the pump handle should be removed in order to prevent further contamination. The board was not convinced, but agreed to remove the pump handle as a precaution. The epidemic quickly subsided.

27
Q

Who found out how infection (syphilis) was transmitted

A

John Hunter

28
Q

Who founded the concept of antiseptic

A

Joseph Lister

- he introduced phenol which is used to sterilize surgical instruments

29
Q

Who discovered streptomycin

A

Selman Waksman

He was working with soil something and found out about it

30
Q

Who founded infection prevention method by physical measures?

A

John Snow

31
Q

Structure for DNA was discovered by

A

James Watson

32
Q

What forms the cell envelope

A

Cell wall,cell membrane,cytoplasmic membrane

33
Q

All of the following are functiooof the cytoplasmic membrane except

A

a. Electron transport
b. Secretion of extra cellular enzymes and toxins
C. Oxidative phosphorylation
D. Uptake of nutrients
E. Protecting the cell

34
Q

Peptidoglycan layer of the Gram positive bacteria is made up of

A

of repeating units of N-acetyl glucosamine and N-acetylmuramic acid linked in a chain

35
Q

Importance of the endotoxins

A

They are released when the bacteria cell membrane breaks down or lysis)lyses) and are responsible for the pathogenesis of gram negative bacteria ( the mechanism by which the bacteria causes illness)

Endotoxins also impair the body’s ability in blood coagulation and causes the body to go into shock

36
Q

Bacteria that don’t have cell wall (example mycoplasma) improve the strength of the cytoplasmic membrane by,

A

Adding components like steroids

37
Q

Importance of loose slime which is similar in composition to the capsule which is external to the cell wall in some bacteria

A

Plays a role in attaching the bacteria to the host and protects the cell against desiccation (removal of moisture from the cell)

38
Q

How does the host defend himself or herself against the infection

A

Phagocytosis

39
Q

Ways of differentiating bacteria

A

Capsule / slime or no capsule
Flagella (which is made up of a protein called flagellin - singular (monotrichous)or multiple (peritrichous)
Pili ( made up of protein called pilin) - this is important in adhering bacteria to the host cells. They are important virulent factors
Spores or endospores - If the spores are located terminally(clostridium tetani ), sub terminally (clostridium perfringens) or centrally
(Bacillus anthracis)

40
Q

What form of bacteria are highly resistant

A

Spores or endospores