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Updated: Feb 17, 2026

Isolation and Identification of Waterborne Antibiotic-Resistant Bacteria and Molecular Characterization of their Antibiotic Resistance Genes
Published on: March 3, 2023
Rapid disc diffusion antibiotic susceptibility testing for Pseudomonas aeruginosa, Acinetobacter baumannii and
Michael Hombach1, Marion Jetter1, Nicolas Blöchliger1
1Institut für Medizinische Mikrobiologie, Universität Zürich, 8006 Zürich, Schweiz.
Rapid antibiotic susceptibility testing (rAST) shows feasibility for Acinetobacter baumannii and enterococci within 6-8 hours. This method accurately identifies resistant strains, but requires breakpoint adaptations for reliable clinical interpretation.
Area of Science:
- Clinical Microbiology
- Antimicrobial Resistance
- Diagnostic Technology
Background:
- Antibiotic susceptibility testing (AST) is crucial for guiding antimicrobial therapy.
- Current AST methods, like disc diffusion, often require 18-24 hours for results.
- Faster AST methods are needed to combat rising antimicrobial resistance.
Purpose of the Study:
- To evaluate the feasibility of rapid disc diffusion antibiotic susceptibility testing (rAST) for key Gram-negative and Gram-positive bacteria.
- To assess the early discrimination of resistant bacterial populations from wild-type (WT) populations.
- To determine the need for clinical breakpoint adaptations for accurate rAST interpretation.
Main Methods:
- Tested rAST with 6-8 hour incubation for Enterococcus faecalis, Enterococcus faecium, Pseudomonas aeruginosa, and Acinetobacter baumannii.
- Utilized the WASPLab automation system for incubation and imaging of disc diffusion plates.
- Defined WT and non-WT populations using epidemiological cut-offs.
Main Results:
- rAST achieved >90% readability for A. baumannii and enterococci at 6-8 hours.
- High categorical agreement (95.3-97.4%) was observed between 6-hour rAST and 18-hour AST for these species.
- Vancomycin-resistant E. faecium were clearly separated from WT at 6 hours.
- P. aeruginosa showed lower readability (68.9% at 8 hours) but good agreement (94.8%).
Conclusions:
- Rapid AST is feasible for A. baumannii and enterococci, enabling faster clinical decisions.
- Early discrimination of resistant strains is possible with rAST.
- Adaptation of clinical breakpoints and/or buffer zones is necessary for accurate rAST interpretation, especially for P. aeruginosa.
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