Lecture 3: Microbial Communities Flashcards

1
Q

What are Windogradsky columns, and how are they created?

A
  • Ecosystems created by mixing soil or sediment with water, adding carbon (e.g., cellulose) and nutrients
  • Columns are then sealed and left for extended period
  • RESULT: self-sustaining ecosystem within a confined space.
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2
Q

What role do microbes play in Windogradsky columns, and how do they contribute to the longevity of these ecosystems?

A

Microbes fix carbon and recycle nutrients, allowing these ecosystems to thrive for many years

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3
Q

How is carbon fixation achieved in Windogradsky columns, and what types of microbial layers can be present in these ecosystems?

A
  • Carbon fixation achieved via cyanobacteria
  • Columns can exhibit layers of both aerobes and anaerobes, showcasing a diverse microbial community with different metabolic preferences.
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4
Q

Give examples of both positive and negative interactions in microbial communities

A
  • Positive
    • Toxic product of one organism may be substrate for another
      • EXAMPLE: heterotrophs recycling nutrients n toxic waste of cyanobacteria
  • Negative
    • Competition (species competes w another for substrates)
    • Inhibition (antibiotics produced by one species target another)
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5
Q

How do microbes sense each other?

A

Quorum sensing

  • Bacteria release autoinducers (compound that induces its own production) → allows them to sense population size
    • E.g. acyl-homoserine lactones
  • Once autoinducer reaches a threshold, cells respond
  • RESULT: cells change expression n function
    • E.g. biofilm forming → invasive
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6
Q

Describe quorum sensing n virulence in S.aureus

A
  • S.aureus is opportunistic (takes advantage of weakened immune systems or other factors to cause disease)
  • Quorum sensing
    • Changes expression: adhesive colonizing commensal → invasive aggressive pathogen
  • Age regulatory system
    • 2 component regulatory system based around an operon w 2 promoters
    • Constitutively expresses AgrA, B, C n D
      • AgrD — autoinducing peptide (AIP)
      • AgrB — transmembrane protein, secretes mature AIP
      • AgrC — AIP receptor, binds AIP then phosphorylates AgrA
      • AgrA — response protein, activates P3 producing RNA III
    • Low cell density (low bacteria), low AIP
      • AIP doesn’t bind to AgrC (AIP receptor)
      • No phosphorylation of AgrA, no P3 activation, no RNAIII production
    • Low threshold cell density [biofilm has matured], high AIP
      • AIP activates enough ArgC
      • ArgA phosphorylation
      • P3 activation
      • RNAIII production
    • RNA III acts as regulatory RNA
      • Represses adhesion → stops cell becoming biofilm
      • Induces elements that drive invasion → allows cell to invade cells
      • Carries hld (δ-haemolysin) → damages RBCs to release Fe2+ within Hb
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7
Q

How does RNA III regulate α-hemolysin (hla) expression?

A
  • Forms a 2° n 3° structure
  • 14 hairpins bend n globular shape brings 3’ n 5’ end together
  • Ends bind to hlaA RNA at Shine-Dalgarno (SD) region → translation
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8
Q

What are biofilms?

A

Small clusters of cells, enclosed in a self-producer polymer matrix n attached to a surface

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9
Q

Give 3 examples of implants where biofilms can form, the organisms most commonly associated, and the consequences

A

Implant | Organism | Consequence |
| — | — | — |
| Contact lenses | P. aeruginosa | Keratitis |
| Urinary catheter | E.coli, P. aeruginosa, P. mirabilis | Bacteriuria |
| Joint replacement | S. epidermis, S. aureus | Septicaemia, device failure |

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10
Q

What are the 3 common characteristics of biofilms?

A
  • Cells enclosed in polymer matrix of exopolysaccharides, proteins and nucleic acid
  • Formation initiated by extracellular signals present in the environment
  • Protection against the host immune response, desiccation and biocides (e.g. antibiotics or disinfectants)
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11
Q

What are the 5 stages of biofilm formation?

A
  1. Initial attachment – flagella, type I pili
  2. Irreversible attachment – LPS, Type IV pili
  3. Maturation I – mirocolonies, produce aliginate, repress flagella
  4. Maturation II – Quorum sensing
  5. Dispersion – release planktonic cells
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12
Q

How might interactions of aerobes n anaerobes allow the biofilm to function like an ecosystem?

A
  • Anaerobic environment in the middle of biofilm [anaerobes present]
  • Aerobic environment outside [aerobes present]
  • Aerobic fermentation on the outside produces organic acieds
    • Organic acid degraded into H2
    • H2 used by anaerobes in the enter
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13
Q

What is σ22?

A
  • Sigma factor
  • Encoded by algT in the alginate synthesis operon
  • Regulates (in Pseudomonas aeruginosa)
    • Expression of Type IV pili (tiny hairs that help it move in surfaces)
    • Induction of alginate production (EPS): alginate forms a protective layer → stick together and survive in harsh conditions
    • Repression of flagella expression [bacteria form colonies thus no longer need to swim using flagella]
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14
Q

What is an example of how environmental signals can influence gene expression in bacteria?

A
  • Vibrio parahaemolyticus switch between two flagella systems as it matures
  • Bacteria encounter a surface → interferes with the rotation of their flagella → activation of a secondary flagella system
  • Switch enables swarming motility (bacteria move along a surface in a coordinated manner)
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