Biofilm Antimicrobial Susceptibility Testing: Bridging the Gap Between In Vitro Models and Clinical Practice
This review highlights the fundamental disconnect between standard planktonic AST and the biofilm lifestyle that dominates most clinical infections. Despite decades of biofilm biology research, standardised tools for biofilm-based susceptibility testing remain absent from clinical microbiology laboratories. The author identifies key bottlenecks and proposes pathways toward clinically implementable biofilm AST methods.
The original study
Biofilm antimicrobial susceptibility testing: where are we and where could we be going?
- Authors
- Coenye T
- Journal
- Clinical microbiology reviews
- Type
- Journal Article, Review, Research Support, Non-U.S. Gov't
- PMID
- 37812003
Original abstract
Our knowledge about the fundamental aspects of biofilm biology, including the mechanisms behind the reduced antimicrobial susceptibility of biofilms, has increased drastically over the last decades. However, this knowledge has so far not been translated into major changes in clinical practice. While the biofilm concept is increasingly on the radar of clinical microbiologists, physicians, and healthcare professionals in general, the standardized tools to study biofilms in the clinical microbiology laboratory are still lacking; one area in which this is particularly obvious is that of antimicrobial susceptibility testing (AST). It is generally accepted that the biofilm lifestyle has a tremendous impact on antibiotic susceptibility, yet AST is typically still carried out with planktonic cells. On top of that, the microenvironment at the site of infection is an important driver for microbial physiology and hence susceptibility; but this is poorly reflected in current AST methods. The goal of this review is to provide an overview of the state of the art concerning biofilm AST and highlight the knowledge gaps in this area. Subsequently, potential ways to improve biofilm-based AST will be discussed. Finally, bottlenecks currently preventing the use of biofilm AST in clinical practice, as well as the steps needed to get past these bottlenecks, will be discussed.