Acute Infection Flashcards

1
Q

Which toxin is secreted by the T2SS?

A

Exotoxin A

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2
Q

T2SS secretes toxins where?

A

Into the extracellular space

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3
Q

T6SS is used for what?

A

To secrete effectors into bacterial cells where they can cause cell damage. Effectors that are able to cleave DNA, impact the cell integrity of the target bacterium by interfering with the cell wall/membrane.

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4
Q

T3SS is used for what?

A

To kill eukaryotic cells

To infect effectors directly into eukaryotic cells to harm them

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5
Q

What is the most toxic virulence factor of P.aeruginosa?

A

Exotoxin A

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6
Q

Exotoxin A is secreted by?

A

T2SS

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7
Q

Exotoxin A is toxic how?

A

Cleaves EF2- elongation factor 2 which is needed for translation
Prevents protein synthesis

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8
Q

T2SS secretes exotoxin A where?

A

Into the extracellular space

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9
Q

What are the three domains of exotoxin A?

A

Has a receptor binding domain
Has a translocation domain
Has a catalytic domain

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10
Q

Exotoxin A is what type of toxin?

A

It is a proenzyme

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11
Q

What is the main difference between the effectors of P.aeruginosa T3SS and those of the pathogenic E.coli T3SS?

A

The T3SS of P.aeruginosa only secretes types of 4 effectors which is different to pathogenic E.coli which is able to secrete a range

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12
Q

What are the 4 possible T3SS effectors?

A
STUY
ExoS
ExoT
ExoU
ExoY
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13
Q

A P.aeruginosa never has?

A

Both ExoS and ExoU

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14
Q

Which effectors are very similar and share the same chaperone?

A

ExoS and ExoT

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15
Q

What is the importance of chaperones?

A

To ensure the appropriate delivery of effectors into the eukaryotic cells.

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16
Q

What is the chaperone for ExoS and ExoT?

A

SpcS

17
Q

ExoS and ExoT share the same molecular chaperone known as?

A

SpcS

18
Q

ExoY has which chaperone?

A

No chaperone identified

19
Q

ExoU has which chaperone?

A

SpcU

20
Q

What are the two catalytic domains of ExoS and ExoT?

A

GTPase activating domain- GAP domain

ADPRT: Adenosine diphosphate ribosyltransferase domain

21
Q

What are all the domains present in ExoS and ExoT?

A

CBD- chaperone binding domain
MTD- membrane translocation domain
GAP domain
ADPRT domain

22
Q

Which catalytic domain in ExoS/ExoT is N-terminal?

A

GAP domain

23
Q

Which catalytic domain in ExoS/ExoT is C-terminal?

A

ADPRT domain

24
Q

Describe the structure of ExoS/ExoT?

A
S secretion signal
CBD
MLD
GAP catalytic domain
ADPRT catalytic domain
25
Q

ExoU is only found in strains?

A

Lacking ExoS

26
Q

Chaperone for ExoU?

A

SpcU

27
Q

Catalytic domains of ExoU?

A

Phospholipase domain

28
Q

What does the phospholipase domain do?

A

It can degrade phospholipids
Degrade the eukaryotic cell membrane- interfere with the integrity of the eukaryotic cell membrane and can result in cell death

29
Q

In comparison to ExoS/ExoT what is different about ExoU?

A

It causes rapid cell death

Causes cell death much quicker

30
Q

What is the most toxic T3SS effector?

A

ExoU

31
Q

ExoY chaperone?

A

No chaperone has been identified

32
Q

ExoY catalytic domain?

A

Adenylate cyclase

33
Q

Adenylate cyclase causes?

A

Intracellular cAMP accumulation
This cAMP can lead to the expression of multiple genes regulated by cAMP. Can disrupt the actin cytoskeleton and increase endothelial permeability.

34
Q

What is associated with acute infection?

A

Acute infection is associated with:
T3SS
Virulence factors e.g. T2SS: Exotoxin A, T3SS: Exo T,U,S,Y, virulence factors from QS: hydrogen cyanide etc…
Motility