MIIM - Pathogenesis of Infection - Week 1 Flashcards

1
Q

Describe bacterial transformation.

A

When free DNA is taken up by a recipient bacterial cell and incorporated into its genome, this is known as transformation.

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2
Q

Describe transduction.

A

When a donor bacterial cell is infected with a bacteriophage, the bacterial DNA is incorporated into the bacteriophage genome.
When this bacteriophage infects another bacterial cell, the donor DNA is incorporated into the new bacterial cell genome. This is known as transduction.

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3
Q

Describe conjugation.

A

When pili connect two bacteria, a plasmif is transferred from one to the other.

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4
Q

Describe transposition.

A

A bacterial cell containing a plasmid with a transposon connects via a pilus to another bacteria. The plasmid is exchanged, and the new bacteria has the plasmid with the transposon incorporated into its genome.

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5
Q

Describe Koch’s 4 posulates.

A

-The microorganism must be present in every case of the disease
-The microorganism must be grown in a pure culture from the affected host
-Inoculation of the microorganism into a susceptible host should produce the same disease
-The microorganism must be recovered from the infected host

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6
Q

Name 3 limitations of Koch’s postulates.

A

-Normal microbiota is ineligible
-Fastidious bacteria cause problems
-No animal models for many human diseases

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7
Q

Describe Koch’s molecular postulates (4).

A

-The phenotype under investigation should be associated with pathogenic members of a genus/species
-The gene responsible for the disease symptoms should be found in all pathogenic strains, but not in non-pathogenic strains.
-Inactivation of the gene associated with the suspected virulence trait should lead to the loss of virulence
-Replacement of the mutated gene should restore virulence

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8
Q

Describe endogenous vs exogenous pathogens.

A

Endogenous - other sites on the host
Exogenous - other organisms (people, animals, plants)

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9
Q

Describe the 7 stages of infection. Specify which are symptomatic/asymptomatic.

A

Colonisation
Invasion
Replication
Evasion of innate immunity
Damage host
Dissemination
Immunity

The first 5 can be asymptomatic.
The last two are symptomatic.

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10
Q

What two factors affects the ability of bacteria to colonise?

A

Presence of adhesion receptors
A suitable microenvironment

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11
Q

What does epithelial colonisation depend on?

A

The interaction between ligands called adhesins, found on the microorganism surface, and specific receptoes on the epithelial cell surface.

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12
Q

Why may bacteria need to damage epithelial cells to gain access to receptors?

A

Epithelial cell are often polarised, so receptors may be differently expressed on different surfaces.

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13
Q

How do fimbriae assist in adhesion (4)?

A

Theyre short, rigid, and have a hollow core. The adhesin is on the tip.

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14
Q

Are non-fimbrial adhesions possible?

A

Yes, by using adhesins on their cell wall

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15
Q

What can a glycocalyx contribute to? Name 2 forms of a glycocalyx.

A

It can contribute to non-fimbrial adhesion.
Thet include capsules and slime layers.

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16
Q

Define quorum sensing.

A

Recognition by individual bacteria of chemical signals produced by a population of bacteria.

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17
Q

What happens to metabolic activity within biofilms?

A

It is reduced.

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18
Q

What happens to virulence within biofilms?

A

It increases.

19
Q

Do both gram positive and negative bacteria produce biofilms?

A

Yes

20
Q

How do most invasions into cells occur?

A

By receptor mediated endocytosis

21
Q

Define invasin.

A

Invasins are ligands on bacterial surfaces that induce invasion.

22
Q

Can adhesins induce invasion?

A

Yes, by binding to a receptor associated with the cytoskeleton.

23
Q

How can bacterial entry between cells occur after invasion?

A

Invasion can result in morphological changes to the cell causing shrinkage, leading to entry between cells.

24
Q

What is a requirement for significant replication to take place?

A

It can only occur if the microbe can evade the host immune response.

25
Q

What cells and proteins are apart of the innate immune system, and what cellular barriers does it use?

A

Cells - phagocytes
Proteins - complement system
Barrier - skin, mucosa, antimicrobial molecules

26
Q

What specificity does the innate immune system have?

A

Molecules shared by microbes or damaged host cells.

27
Q

Does the innate immune system have any memory of infections?

A

No

28
Q

What cells and proteins are apart of the adaptive immune system, and what cellular barriers does it use?

A

Cells - lymphocytes
Proteins - antibodies
Barrier - lymphocytes

29
Q

What specificity does the adaptive immune system have?

A

Microbial antigens

30
Q

Does the adaptive immune system have any memory of infections?

A

Yes

31
Q

Define exotoxin.

A

Toxins secreted by bacteria

32
Q

Define endotoxin.

A

Toxins that are integral to the gram-negative cell wall, and not secreted.

33
Q

Can exotoxins be inactivated by heat?

A

Yes

34
Q

Do exotoxins have high or low potency?

A

High

35
Q

Are endotoxins cytotoxic?

A

Yes

36
Q

Can antigens be made against exotoxins?

A

Yes

37
Q

How do endotoxins become problematic?

A

When gram-negative bacteria die, they are released.

38
Q

Can endotoxins be inactivated by heat?

A

No

39
Q

Can antigens be made against endotoxins?

A

No

40
Q

Are endotoxins hydrophobic or water soluble?

A

Water soluble

41
Q

Describe dissemination. How can it cause damage?

A

Spreading to other tissues. Can cause damage when organisms produce enzymes that damage cells to allow further spread.

42
Q

Give an example of an endotoxin.

A

Lipopolysaccharide A

43
Q

Briefly describe how a biofilm can be established.

A

-Microbes attach to a surface
-They bind to a conditioning film
-More bacteria arrive an a biofilm forms