Lecture 2 Flashcards

(50 cards)

1
Q

What must bacteria maintain and why?

A

Bacteria must maintain a reservior.
Some bacterial pathogens can move from human to human, human to animal but many don’t.

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2
Q

Do pathogens spend extended periods of time in the external environment

A

Yes

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3
Q

What are some major issues with bacteria maintaining a reservoir?

A
  • Availability of essential nutrients
  • Lack of adherence sites or niches similar to hosts (Surviving in amoeba is similar to immune cells)
  • Exposure to noxious chemicals/predators
  • Exposure to sunlight and extreme weather (Thermal shifts)
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4
Q

What are some survival strategies for bacteria?

A
  • Endo-sporulation (Gram positive)
  • Desiccation resistance (Gram Negative)
    -Metabolic versatility
  • Dormancy
  • Genome plasticity
  • Colonize another host
  • Alter membrane properties
  • Xenobiotic efflux
  • Biofilm formation
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5
Q

What is endo-sporulation (gram positive)

A
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6
Q

What is desiccaton resistance (Gram negatvie)

A

The cell not drying out, there are molecules that bacteria produce that help them retain water and resist the absence within cells

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7
Q

What is metabolic versatility?

A
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8
Q

What is dormancy

A

A way that bacteria responds to starvation, they can survive for extended periods of time without external nutrients

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9
Q

What is genome plasticity

A

Where bacteria can rearrange their genes in a particular way; they can acquire new things and/or survive in a new host.

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10
Q

What does colonize another host mean

A
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11
Q

What is motility and chemotaxis?

A
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12
Q

What does it mean to alter membrane properties

A

To shift composition of the cell envelope in a particular way to survive within the presence of particular chemicals

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13
Q

What is xenobiotic efflux

A

Taking a toxic compound and blow it outside of a cell.

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14
Q

What is biofilm formation

A
  • Can act as a reservoir to many bacteria
    -viewed as a developmental and social process that is functionally analogous to differentiation in multicellular organisms
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15
Q

Explain biofilm formation

A
  • Many bacteria form biofilms
  • They are dense, multiorganismal layers of bacterial communities attached to surfaces
  • Biogilm protect against antibiotics, disionfectants, phagocytic attack and more
  • Bacterial attachment to surgace.each other is mediated by polysaccharide slime, which acts like a glue
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16
Q

What is biofilm matrix polymers and what do they do

A
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17
Q

What is Molecular Koch’s postulates

A

This is proof that a gene product is an essential virulence factor

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18
Q

What are the steps of Molecular Koch’s postulates?

A
  1. The pathogenic trait should be associated with the pathogenic members of the genus, species or strains
  2. Inactivation of the gene associated with the pathogenic trait should result in a measurable loss of pathogenicity or virulence
  3. Reversion of allelic replacement (complementation) of the mutated gene should restore pathogenicity
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19
Q

What is an example of molecular Koch’s postulates

A

This is more than an organism infecting a host.
- Start by inactivating the gene that’s linked to the specific trait, you would knock out the gene from the protein and show there is a virulence-associated phenotype in an animal model.
Then replace the allele back inside bacteria and it would restore virulence (This is important because it confirms that genetic linkage is sound and there is no mutation that occurred)

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20
Q

How do we evaluate virulence factors?

A

By compairng the ability of the wildtype and mutant bacteria to survive in a host and cause disease

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21
Q

What are the 4 steps we use to evaluate virulence factors?

A
  1. dilute bacteria to known concentration
  2. Infect host (assess the success of initial inoculation)
  3. Allow animals to get sick (wild type takes a few days)
  4. Harvest organs and assess bacterial growth and pathology
22
Q

What are the 5 common steps in bacterial infection

A
  1. Entry to the host body for colonization
    - Migration to a niche
    - Often requires attachment
  2. Evasion of host defenses (innate and adaptive)
  3. Obtain nutrients, multiply to significant numbers, and spread
  4. Damage the host and produce disease
    - Direct damage due to toxins of the bacteria
    - Collateral damage due to immune response
  5. Transmission from infected to susceptible host
23
Q

Explain (1) entry into the host and the ways it occurs

A

There is no known bacterium tha can penetrate human skin.
Entry occurs via:
Wounds and burns
Insect bites
Ingestion of tainted foods
The eyes
Inhalation
Genitourinary tract

24
Q

Explain motility and taxis in relation to entry into the host

25
What is flagella
Long (up to 20 um) helical structures extending outward from the cell surface - polymers of flagellin protein - Evolutionarily conserved (they are mediators for immune recognition and attachment) - Mediate movement in fluids
26
How is motility directed
Motility is often directed by the ability to sense chemical (chemotaxis), light (phototaxis), oxygen (aerotaxis) or magnetic fields (magnetotaxis) Sensing is followed by directional swimming towards or away from the signal being sensed
27
What is E.coli UTIs an example of
Urine is nutrient-rich E. coli can gain access to bladder Bladder periodically cleansed by urination Combination of motility and chemotaxis
28
What is an evasion of host defenses?
Bacteria will often bind to specific cell types to gain entry into a target tissue or remain in a niche many parts of the body are protected by mucus (mucus: a mesh of proteins and polysaccharides (Glycoproteins on mucosal surfaces)
29
Explain (2) Evasion of host defenses
30
What is the function of mucin
- Acts as lubricant but also traps bacteria (an example would be in the hollows of the GI tract) - Prevents microbes from accessing/binding to first layer of cells (first layer is epithelial cells) - It is expelled by goblet cells - Is non-uniform (patchy)
31
What is lamina propria?
refers to the thin layer of loose connective tissue underneath the epithelial cells. This can be a site of infection
32
How might bacteria penetrate through mucin?
33
What must bacteria do once past mucin?
Bacteria must remain in place without being dislodged (coughing, peristalsis, swallowing, urination) Adherence is the essential first step in initiating disease
34
What are some strategies for adhesion?
Flagella Pilli Fimbriae Afrimbrial adhesins
35
What is host and tissue tropism
Refers to how different viruses/pathogens have evolved to preferentially target specific host species, a species tissue, or a species cell type within the host Tropsim is driven by molecular interactions between pathogen and host. Adhesion between ligands on the bacterium and receptors on the host (or vice-versa) lie at the root of tropism
36
What are antimicrobial peptides? Provide an example
37
What are defensins
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