Chapter 10: Community Lifestyle of a Biofilm
Learning Objectives
Describe biofilm characteristics and formation
Differentiate biofilms from planktonic cultures
Explain features contributing to persistence and antimicrobial resistance in biofilms
Understand quorum sensing and chemotaxis in E. coli
Apply knowledge of E. coli systems to other bacteria
Interpret data on biofilms, quorum sensing, and chemotaxis
Bacteria and Biofilms
Biofilms are organized bacterial communities adhered to surfaces, surrounded by extracellular polymeric substances (EPS).
EPS consists of polysaccharides, proteins, and nucleic acids; biofilms can contain one or multiple species of bacteria.
Biofilm formation involves quorum sensing mediated by autoinducers leading to coordinated growth, maturation, and dispersion.
Planktonic bacteria are free-floating and can join or be part of a biofilm.
Prevalence of Biofilms
Biofilms account for 65-80% of bacterial infections; they can be benign or pathogenic.
Benign examples: environmental biofilms on surfaces (e.g., rocks, ships).
Pathogenic examples: biofilms on medical devices cause significant infections (e.g., urinary catheters, dental implants).
Chronic infections (e.g., cystic fibrosis) are often biofilm-associated.
Treating Biofilms
Antimicrobial Resistance
Biofilms exhibit >10,000 times more resistance to antibiotics compared to planktonic bacteria.
Key resistance factors: EPS matrix, nutrient/O2 gradients, presence of persister cells.
New Pharmaceutical Approaches
Strategies include interfering with EPS, inhibiting adherence, and targeting autoinducers.
Quorum Sensing
Quorum sensing allows bacteria to respond to population density using autoinducers to regulate gene expression.
In E. coli, the Lsr system regulates AI2 signaling, influencing community behaviors.
LsrR acts as a global regulator and is crucial for responding to AI2 concentration changes.
Bacterial Motility and Chemotaxis
Chemotaxis allows bacteria to navigate towards attractants or away from repellents.
Spatial and temporal sensing mechanisms enable bacteria to detect chemical concentration gradients.
E. coli motility involves runs and tumbles, with flagellar rotation directing movement.
Chemotaxis in E. coli
Involves chemoreceptors that, when activated by signals, alter flagellar rotation by phosphorylating response regulators like CheY.
Chemotactic responses include adjusting movement based on environmental cues, impacting interactions with chemicals.
Conclusion
Understanding biofilms, quorum sensing, and chemotaxis is crucial for addressing bacterial behavior in clinical and environmental contexts.