Target intelligence / Profile preview

Biofilm-forming bacteria

Molecular classification
Other
01

Overview

Biofilm-forming bacteria are microorganisms that transition from a planktonic state to a sessile community encased within a self-produced extracellular polymeric substance (EPS) matrix (StatPearls, 2023). This matrix, composed of polysaccharides, proteins, and extracellular DNA, provides a robust physical barrier that protects the bacteria from environmental stressors, host immune cells, and antibiotic penetration (Nature Reviews Microbiology, 2022). Biofilms are a primary driver of chronic and healthcare-associated infections, particularly those involving prosthetic joints, catheters, and the respiratory tracts of patients with cystic fibrosis (NIH, 2021). Pharmacological strategies to combat these bacteria include the use of matrix-degrading enzymes, quorum-sensing inhibitors to disrupt communication, and high-concentration antibiotic regimens (Frontiers in Microbiology, 2018). Because biofilm-forming bacteria refers to a complex multicellular phenotype across various species rather than a single molecular entity, it is considered a therapeutic category rather than a specific molecular target.

Other names
Biofilm-producing bacteriaSessile bacteriaMicrobial biofilmsSlime-producing bacteria
02

Mechanism of action

Drugs targeting biofilm-forming bacteria act by inhibiting initial surface attachment, disrupting quorum-sensing communication (cell-to-cell signaling), degrading the extracellular polymeric substance (EPS) matrix, or penetrating the metabolic dormancy of sessile cells (Journal of Antimicrobial Chemotherapy, 2015).

03

Biological functions

AdhesionQuorum sensingExtracellular polymeric substance (EPS) productionAntimicrobial resistanceMetabolic dormancyHorizontal gene transfer
04

Disease associations

InfectionCystic fibrosisEndocarditisPeriodontitisChronic wound infectionCatheter-associated urinary tract infection (CAUTI)
05

Safety considerations

Potential for systemic dissemination of bacteria (sepsis) during therapeutic biofilm dispersal (Nature Reviews Drug Discovery, 2013)Increased risk of antibiotic toxicity due to high dosing requirements (Journal of Antimicrobial Chemotherapy, 2015)Selection of highly resistant persister cellsDisruption of commensal microbiota
06

Interacting drugs

Tobramycin

5 more in the full profile.

07

Biomarkers

Acyl-homoserine lactones (AHLs) (Clinical Microbiology Reviews, 2010)Extracellular DNA (eDNA) levels (Frontiers in Microbiology, 2018)Biofilm-specific antibodies (e.g., anti-alginate antibodies) (Journal of Clinical Microbiology, 2014)Procalcitonin (StatPearls, 2023)C-reactive protein (CRP) (StatPearls, 2023)

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