1.8. Microbes and biofilm concept Flashcards

1
Q

describe the composition and structure of a biofilm

A
  1. enclosed by self-produced EPSs matrix
  2. irreversibly associated to each other and/or to a surface
  3. may form on biotic/ abiotic surfaces –> present in all settings
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2
Q

what is a biofilm?

A

aggregates of micro-organisms

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3
Q

what is EPS?

A

EPS are slime produced for protection

  1. extracellular polysaccharides
  2. structural proteins
  3. lipids
  4. nucleic acids (DNA & RNA)
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4
Q

list in sequence and describe each step in biofilm formation

A
  1. initial reversible attachment (weak van der Waal forces & hydrophobic effect)
  2. irreversible attachment (pili, fimbriae)
  3. micro-colony (growth & cell division)
  4. maturation (EPS produced)
  5. dispersion
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5
Q

differentiate planktonic & sessile microbial cells

A
  1. planktonic = free-floating
  2. sessile = communities –> more properties than planktonic:
    sessile can up/downregulate gene function–> can save significant amounts of energy
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6
Q

describe how biofilm multicellularity protects against antimicrobial agents

A
  1. less susceptible to antimicrobial agents

2. microorganisms protected by multicellular biofilm construct

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7
Q

quorum-sensing (communication)

A
  1. auto-inducer concentrations amongst cells in tight-knit biofilm are used as communication
    - ->synchronise activities of large microbe group
    - -> biofilm microbes can alter behaviour on a population-wide scale in response to change in number and/or species present in the community
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8
Q

autoinducers

A
  • small, hormone-like molecules
    1. synthesized intracellularly by microbes
    2. actively secreted/ passively released from microbes
    3. [extracellular AI] increases with increase in number of microbes in population
    4. population-wide changes triggered by signal transduction cascade when AIs accumulate above threshold level required for detection & receptors bind the AIs
    5. sessile microbial cells => EPS –> cells in close proximity => [signal molecule] builds up => changes cell behaviour
    6. some bacterial pathogens do not produce toxins until they have large enough population to survive host’s defence mechanisms
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9
Q

discuss the importance of biofilms in infectious diseases

A
  1. Device-related biofilm infections
    - Biofilms occur on or within indwelling medical devices
  2. Non-device related biofilm infections
    - Biofilms that form directly on host tissues
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10
Q

Main nosocomial infections associated with biofilms

A
  1. Bacteraemia
    - 87% of bacteraemias have an indwelling vascular device
  2. Urinary tract infections
    - 95% of UTIs are catheter-related
    - Risk of UTI increases by 5% for each day the catheter is in situ
  3. Pneumonia
    - Incidence of ventilator-associated pneumonia ranges from 7% to > 40%
  4. Surgical wound infections
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11
Q

current approaches to management of biofilm-related infections

A
  • Rigorous antisepsis
  • Early detection and treatment
  • Removal/replacement of foreign bodies/catheters
  • Antibiotics
  • Anti-quorum-sensing drugs (e.g. Macrolide antibiotics)
  • Antimicrobial impregnated devices
  • Antimicrobial lock therapy
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12
Q

novel & future approaches to management of biofilm-related infections

A
  • Sonication of indwelling devices (implants or prostheses or catheters) from patients with suspected infection to improve the detection rate of bacteria
  • Substances able to destroy biofilm EPS matrix (e.g. dispersin B)
  • Substances which destroy persister cells
  • Quorum-quenching enzymes
  • Substances which cause biofilm self-destruction (e.g. phage therapy)
  • Strategies to enhance the activity of conventional antimicrobial agents (e.g., electrical current, radiofrequency, electromagnetic fields, ultrasound)
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