Bundeswehr Institute of Microbiology, Central Diagnostic Unit, Munich, Germany.
Istituto Zooprofilattico Sperimentale della Puglia e della Basilicata, Anthrax Reference Institute, Foggia, Italy.
Clin Microbiol Infect. 2024 Sep;30(9):1170-1175. doi: 10.1016/j.cmi.2024.05.019. Epub 2024 Jun 7.
Bacillus anthracis clinical breakpoints, representing a systematic approach to guide clinicians in selecting the most appropriate antimicrobial treatments, are not part of the guidance from the European Committee on Antimicrobial Susceptibility Testing (EUCAST). This is because defined distributions of MIC values and of epidemiological cut-off values (ECOFFs) have been lacking. In this study, a Europe-wide network of laboratories in collaboration with EUCAST, aimed at establishing standardized antimicrobial susceptibility testing methods, wild-type MIC distributions, and ECOFFs for ten therapeutically relevant antimicrobials.
About 335 B. anthracis isolates were tested by broth microdilution and disc diffusion methodologies. 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.
Broth microdilution and disc diffusion data distributions revealed putative wild-type distributions for the tested agents. For each antimicrobial agent, ECOFFs were defined. Three highly resistant strains with MIC values of 32 mg/L benzylpenicillin were found. MIC values slightly above the defined ECOFFs were observed in a few isolates, indicating the presence of resistance mechanisms to doxycycline, tetracycline, and amoxicillin.
B. anthracis antimicrobial susceptibility testing results were used by EUCAST to determine ECOFFs for ten antimicrobial agents. The MIC distributions were used in the process of determining clinical breakpoints. The ECOFFs can be used for the sensitive detection of isolates with resistance mechanisms, and for monitoring resistance development. Genetic changes causing phenotypic shifts in isolates displaying slightly elevated MICs remain to be investigated.
炭疽杆菌临床折点代表了一种系统的方法,旨在指导临床医生选择最合适的抗菌治疗方法,但它不是欧洲抗菌药物敏感性测试委员会(EUCAST)指南的一部分。这是因为缺乏已定义的 MIC 值分布和流行病学折点(ECOFF)。在这项研究中,一个由实验室组成的欧洲网络与 EUCAST 合作,旨在建立标准化的抗菌药物敏感性测试方法、野生型 MIC 分布和十种治疗相关抗菌药物的 ECOFF。
采用肉汤微量稀释法和纸片扩散法对约 335 株炭疽杆菌进行了检测。MIC 和抑菌圈直径根据 EUCAST SOP 10.2 进行了整理,结果提交给 EUCAST 以确定 ECOFF 和临床折点。
肉汤微量稀释和纸片扩散数据分布显示出所测试药物的野生型分布。为每种抗菌药物定义了 ECOFF。发现了 3 株 MIC 值为 32mg/L 苯唑西林的高度耐药菌株。在少数分离株中观察到略高于定义的 ECOFF 的 MIC 值,表明存在对强力霉素、四环素和阿莫西林的耐药机制。
EUCAST 使用炭疽杆菌抗菌药物敏感性测试结果来确定十种抗菌药物的 ECOFF。MIC 分布用于确定临床折点的过程中。ECOFF 可用于敏感检测具有耐药机制的分离株,并用于监测耐药性的发展。导致分离株表型变化的遗传变化导致 MIC 值略升高,仍需进一步研究。