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. 2025 Sep 11:S1198-743X(25)00451-3.
doi: 10.1016/j.cmi.2025.09.001. Online ahead of print.

Defining epidemiological cut-off (ECOFF) values for Brucella melitensis: An European multi-centre study

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Free article

Defining epidemiological cut-off (ECOFF) values for Brucella melitensis: An European multi-centre study

Flavia Dematheis et al. Clin Microbiol Infect. .
Free article

Abstract

Objectives: Brucellosis in humans is mainly caused by B. melitensis and is associated with a risk of chronic infections and relapses. For appropriate patient treatment decisions and outcomes, clinical breakpoints are needed as well as standard antimicrobial susceptibility testing (AST) procedures. In this study a Europe-wide network of Brucella reference laboratories aimed, in close collaboration with EUCAST (the European Committee on Antimicrobial Susceptibility Testing), at establishing standardized AST methods, wild-type (WT) MIC and zone diameter distributions and to set epidemiological cut-off (ECOFF) values for nine therapeutically relevant antimicrobial agents.

Methods: A total of 499 B. melitensis strains were tested at six study centres by broth microdilution (BMD) and disc diffusion (DD). Minimum inhibitory concentrations (MIC) and inhibition zone diameters were curated according to EUCAST SOP 10.2 and the results were submitted to EUCAST for ECOFFs and clinical breakpoint determination.

Results: BMD and DD data distributions revealed putative WT distributions for the tested antimicrobial agents. MIC ECOFFs were determined for all agents based on five to six distributions, encompassing 249-499 observations. Six isolates showed MIC values slightly above the ECOFFs, indicating the presence of potential resistance mechanism to rifampicin, streptomycin and trimethoprim-sulfamethoxazole. Zone diameter ECOFFs were established for rifampicin and ceftriaxone, while tentative (t)ECOFFs were determined for ciprofloxacin, levofloxacin, gentamicin and streptomycin.

Conclusions: Standardized BMD and DD methodologies for B. melitensis were validated and AST results were used by EUCAST to set ECOFFs. Based on these, clinical breakpoints were released in v14.0 of the EUCAST clinical breakpoints table, enabling sensitive detection of resistance mechanisms and monitoring of resistance development. Genetic changes in isolates with slightly elevated MICs remain to be investigated.

Keywords: Antimicrobial susceptibility testing; Brucella melitensis; Epidemiological cut-off value; Wild-type MIC distributions; clinical breakpoints.

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Conflict of interest statement

Conflicts of Interest The authors have no relevant financial or non-financial interests to disclose.

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