LG5.9 bact virulence strat Flashcards

1
Q

Define virulence.

A

•extent of pathogenicity –E.g. number of virulence factors

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2
Q

Where are bacterial virulence genes located?

A
  1. chromosome (pathogenicity islands - these can also be on plasmids). they are unique region exclusively associated w/ virulence - complete island required for delivery of pathogenic trait
  2. plasmids
  3. inside bacteriophages
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3
Q

Discuss how bacterial cells adhere to host cells.

A

–bacterial adhesin↔host receptor

bacteria use ‘adhesin’–E.g. •pili, OM proteins/sugars, CW proteins, teichoic acids

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4
Q

what are hydrolytic enzymes? what’s their role as a virulence factor?

A
  • chew up material - help with digestion and digging into tissues (invasiveness) (eg, proteases, hemolysins, neuroaminidase, collagenase, DNase, etc.
  • Cause host tissue Injury
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5
Q

Give some characteristics of exotoxins

A
  • these are virulence strategy (tissue injury)
  • secreted
  • Gr+ or Gr-
  • protein
  • causes fever somtimes
  • neutralized by antitoxin

LD50 is small

-most heat-sensitve

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6
Q

Give some characteristics of Endotoxins

A

these are virulence strategy (tissue injury)

  • on OM
  • Gr- only
  • Lipid A constituent
  • always causes fever
  • not neutralized by antitoxin

LD50 is large

-most heat-stable

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7
Q

List some types of extoxins

A
  • A-B exotoxins (B ‘B’inds to specific host receptors) (A (‘A’ctive) enters cell and enzymatically attacks host function or structure (eg Vibrio cholerae A-B enterotoxin)
  • pore-forming exotoxins
  • superantigens
  • type III secretion system
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8
Q

What are superantigens?

A

-Exotoxin (virulence factor that causes tissue injury)

•non-specific activation of T-cells resulting in polyclonal T cell activation and massive cytokine release

(bind MHC molecules on antigen presenting cells (w/o processing) and directly stimulate cytokine production→ massive activation of T cells→ uncontrolled release of cytokines→ inflammation→ shock)

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9
Q

What are type III secretion systems?

A

-exotoxin (virulence factor that causes tissue injury)

»only in Gr-

»‘syringe’ for injecting toxic molecules into host cells (traverse envelope)

-never exposed to immune system

»no virulence w/o

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10
Q

Why is do some bacteria thrive INSIDE of host cells?

A
  • easier to evade host defenses INSIDE of our cells vs outside
  • facultative intracellular
  • obligate intracellular
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11
Q

how do capsules protect some bacteria?

A

-virulent strategy (evading host defense)

  • interferes w/ complement deposition
  • interferes w/ phagocyte engulfment
  • eg, Streptococcus pneumoniae
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12
Q

List six ways bacteria evade the host immune system

A
  • invade cells
  • capsules

–phase variation eg, Neisseria gonorrhoeae

–antigenic variation eg, Neisseria gonorrhoeae

–IgA1 protease eg, mucosal pathogens, Neisseria gonorrhoeae

–biofilms - common strategy!

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13
Q

How is antibiotic resistance used as a virulence strategy?

A

–innate (eg mycoplasma has no cell wall - so Antibx that target cell wall won’t work)

–acquired (mutation, gene exchange)

–biofilms

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14
Q

what is phase variation?

A
  • way to ‘evade host defese’
  • bacteria’s ability to turn on and off its surface molecules so the bacteria will look different during infection

eg, Neisseria gonorrhoeae

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15
Q

what is antigenic variation?

A
  • way to evade host defense
  • bacteria’s ability to change surface antigens

eg, Neisseria gonorrhoeae

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16
Q

what is IgA1 protease?

A

this clips the antiody at the hinge

eg, mucosal pathogens, Neisseria gonorrhoeae

17
Q

What are 2 virulence factors that help bacteria gain entry to the cell?

A

–phagocytes (capsules)

–host iron-binding molecules (bacterial virulence factor known as ‘siderophore’)