1.8. Microbes and biofilm concept Flashcards
1
Q
describe the composition and structure of a biofilm
A
- enclosed by self-produced EPSs matrix
- irreversibly associated to each other and/or to a surface
- may form on biotic/ abiotic surfaces –> present in all settings
2
Q
what is a biofilm?
A
aggregates of micro-organisms
3
Q
what is EPS?
A
EPS are slime produced for protection
- extracellular polysaccharides
- structural proteins
- lipids
- nucleic acids (DNA & RNA)
4
Q
list in sequence and describe each step in biofilm formation
A
- initial reversible attachment (weak van der Waal forces & hydrophobic effect)
- irreversible attachment (pili, fimbriae)
- micro-colony (growth & cell division)
- maturation (EPS produced)
- dispersion
5
Q
differentiate planktonic & sessile microbial cells
A
- planktonic = free-floating
- sessile = communities –> more properties than planktonic:
sessile can up/downregulate gene function–> can save significant amounts of energy
6
Q
describe how biofilm multicellularity protects against antimicrobial agents
A
- less susceptible to antimicrobial agents
2. microorganisms protected by multicellular biofilm construct
7
Q
quorum-sensing (communication)
A
- 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
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
9
Q
discuss the importance of biofilms in infectious diseases
A
- Device-related biofilm infections
- Biofilms occur on or within indwelling medical devices - Non-device related biofilm infections
- Biofilms that form directly on host tissues
10
Q
Main nosocomial infections associated with biofilms
A
- Bacteraemia
- 87% of bacteraemias have an indwelling vascular device - Urinary tract infections
- 95% of UTIs are catheter-related
- Risk of UTI increases by 5% for each day the catheter is in situ - Pneumonia
- Incidence of ventilator-associated pneumonia ranges from 7% to > 40% - Surgical wound infections
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
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)