Quorum sensing Flashcards

1
Q

processes dependent on sufficient population size

A

virulence factor production

biofilms

bioluminescence

ABs

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2
Q

bacterial communication

  • mediated by
  • signal intensity shows
  • used to regulate…?
A

production + sensing of chemical signals

population density

gene expression

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3
Q

symbiotic example

  • what is it?
  • benefits
A

V. fischeri colonise specialised crypt (light organs) of bobtail squid

bacteria - get nutrients
squid - get bioluminescence
(counter-illumination)

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4
Q

V. fischeri

- when do they produce light?

A

at certain cell density
- waste of time to produce if just 1 cell

only in squid
- squid survives -> bacteria survive

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5
Q

quorum sensing

A

LuxI produces autoinducer molecules (Als)

favourable enviro -> bacteria increase -> more Als

  • > activates LuxR
  • > transcribes genes
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6
Q

autoinducers (AIs)

  • what are they?
  • types in Gram -ve and +ve
  • universal types
A

signalling molecules
- same core region but different chain lengths

Gram -ve
= acyl-homoserine lactones

Gram +ve
= oligo peptides

Universal
= furanosyl borate diester

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7
Q

QS systems

- 3 key principles

A
  1. members of community generate AIs
  2. AIs detected by receptors on membrane/in cytoplasm
  3. AI detection
    -> further AI production (feed-forward effect)
    + activation of QS regulated traits
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8
Q

feed forward effect

A

increases signal intensity
-> facilitates synchronisation

(all cells in population can detect AIs + upregulate gene expression)

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9
Q

2 component systems
- what do they do?

  • most common e.g.
A

senses external signals + relays into cell

sensor kinase (SK) system

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10
Q

sensor kinase system

A
  1. SK recognises signal
  2. internal kinase domain phosphorylated at His residue
  3. interacts with response regulator + transfers P
  4. active response regulate modulates gene expression
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11
Q

2nd component of SK system

A

response regulator

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12
Q

QS control of virulence in P. aeruginosa

A

opportunistic G-ve pathogen

in CF lung infections

forms biofilm

virulence regulated by QS
- 3 circuits interact

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13
Q

P. aeruginosa

- 3 interacting circuits

A

las IR circuit
rhl IR circuit
PQS circuit

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14
Q

exploiting QS to control bacteria

  • QS interfering drug
  • key principle
A

Las + Rhl
= targets for anti-virulence/ anti-biofilm agents
-> develop receptor inhibitors

disrupt bacterial communication + coordination of gene expression

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15
Q

G+ve QS systems

A

AIPs synthesised as inactive precursors

-> activated in transporter or after secretion

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16
Q

S. aureus

A

commensal

- opportunistic

17
Q

QS in S. aureus

A

low densities
= low AI conc
-> cells express adhesins
.:. stick during initial phases of infection

high densities
= high AI conc
-> express toxins
.:. release more nutrients + move to new site