Virulence II Flashcards

1
Q

List the 4 stresses that V. cholerae must survive to cause disease.

A
  • ingested via contaminated food or water
  • survive low pH of the stomach
  • have adhesive/invasive properties in order to colonize small intestine
  • produce and excrete toxin
  • disseminate watery diarrhea
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2
Q

List the 2 subunits of cholera toxin and their roles in producing diarrhea.

A

2 Alpha subunit

  • encoded for by ctxA gene
  • cleaved to reveal active A1 subunit
  • catalyzes ADP-ribosylation of Gas => activates AC => cAMP => PKA
  • phosphorylation of proteins involved in intestinal ion transport => water leaks into lumen
  • severe watery diarrhea

5 Beta subunit

  • encoded for by ctxB gene
  • required for A1 toxin to be secreted out of the bacterial cell
  • 5 subunits act as scaffold to hold A2-A1
  • required for interaction with host cell surface receptor GM1 glycoprotein
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3
Q

List 3 other virulence factors, their roles, and the genes that encode them.

A
  1. TCP-ACF => motility and adhesion
  2. ToxR => toxR => global regulator (TM)
  3. ToxS => toxS => environmental sensor (TM)
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4
Q

Describe how ToxR and ToxT regulated the ToxR regulon.

A
  • toxR and toxS form an operon

- transcription is regulated by temperature

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5
Q

Describe how temperature can regulate the ToxR regulon.

A

low temperature = operon is ON
=> toxRS transcribed, synthesized and localized to cytoplasmic membrane

high temperature in upper GI = operon is OFF
=> no further toxRS transcribed; but proteins already on the membrane remain there (basal level)

high temperature in intestines = signals ToxS

  • communicates with ToxR
  • cytoplasmic domain of ToxR binds to TCP-ACF element
  • activates TCP-ACF
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6
Q

ADP-ribosylation of the Gas protein results in the activation of what host enzyme?

A
  • adenylate cyclase
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7
Q

Describe the TCP-ACF element.

A
  • TCP (toxin co-regulated pilus) encodes for flagellum to allow motility into colonization site
  • ACF (accessory colonization factor) encodes for adhesins/invasins to colonize the site
  • mutations in these genes decrease virulence
  • TCP-ACF element is a large pathogenicity island where both genes are located
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8
Q

How does transduction play a role in disseminating cholera?

A

V. cholerae requires transduction by phage carrying ctx genes to produce toxin

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9
Q

Describe the function of ToxR, ToxS, ToxT.

A
  • ToxS sense the environment and activates ToxR in the high temperatures of the intestine
  • ToxR is a transcription factor that activates TCP-ACF-ToxT element
  • ToxT autoregulates by regulating the ToxR operon and the CTX operon
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10
Q

How does ToxT autoregulate?

A
  • part of tcp domain
  • activated by ToxR
  • ToxT is an activator that controls ToxR regulon
  • thus autoregulates since tcp is part of ToxR regulon
  • activates many other operons, including ctx
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11
Q

If the toxT gene were deleted, which of the following genes would have their transcription affected? not affected?

  • toxT
  • toxS
  • tcp
  • acf
  • ctxB
A
  • toxT, ctxB, tcp-acf

- toxS unaffected

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12
Q

Describe Vibrio cholerae.

A
  • highly motile
  • uniflagellated
  • gram (-)
  • curved rod
  • extracellular pathogen
  • causes cholera (life-threatening diarrheal disease that can rapidly attain epidemic proportions; transmitted through unsanitary food)
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13
Q

Describe the role of the flagellum in V. cholerae colonization.

A
  • required for virulence
  • regulatory network alternates expression of motility genes and toxin genes
    ==> first, motility to get to colonization site. THEN toxin genes to cause disease
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