Antimicrobial Tolerance in Biofilms

• Published in: Microbiology spectrum Vol. 3; no. 3
• Main Author: Stewart, Philip S
• Format: Journal Article
• Language: English
• Published: United States ASM Press 01.06.2015
• Subjects: Anti-Bacterial Agents; Anti-Bacterial Agents - pharmacology; Bacteria; Bacteria - drug effects; Bacteria - pathogenicity; Biofilms; Biofilms - drug effects; Biofilms - growth & development; Disinfectants; Disinfectants - pharmacology; Drug Resistance, Bacterial; Drug Resistance, Bacterial - physiology; Microbial Sensitivity Tests; Review Article
• ISSN: 2165-0497; 2165-0497
• DOI: 10.1128/microbiolspec.mb-0010-2014

The tolerance of microorganisms in biofilms to antimicrobial agents is examined through a meta-analysis of literature data. A numerical tolerance factor comparing the rates of killing in the planktonic and biofilm states is defined to provide a quantitative basis for the analysis. Tolerance factors for biocides and antibiotics range over three orders of magnitude. This variation is not explained by taking into account the molecular weight of the agent, the chemistry of the agent, the substratum material, or the speciation of the microorganisms. Tolerance factors do depend on the areal cell density of the biofilm at the time of treatment and on the age of the biofilm as grown in a particular experimental system. This suggests that there is something that happens during biofilm maturation, either physical or physiological, that is essential for full biofilm tolerance. Experimental measurements of antimicrobial penetration times in biofilms range over orders of magnitude, with slower penetration (>12 min) observed for reactive oxidants and cationic molecules. These agents are retarded through the interaction of reaction, sorption, and diffusion. The specific physiological status of microbial cells in a biofilm contributes to antimicrobial tolerance. A conceptual framework for categorizing physiological cell states is discussed in the context of antimicrobial susceptibility. It is likely that biofilms harbor cells in multiple states simultaneously (e.g., growing, stress-adapted, dormant, inactive) and that this physiological heterogeneity is an important factor in the tolerance of the biofilm state.