Maynard Richard, Manuel Carmila, Simpkins Synthia, Haro Michelle, Ledeboer Nathan, Simner Patricia J, Fisher Mark, Humphries Romney
Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J Clin Microbiol. 2025 Jun 11;63(6):e0011525. doi: 10.1128/jcm.00115-25. Epub 2025 May 14.
spp. are uropathogenic gram-positive bacteria that occasionally cause invasive infections. Minimal inhibitory concentration (MIC) breakpoints published by the Clinical and Laboratory Standards Institute (CLSI) were evaluated, and disk diffusion criteria developed, by testing 174 isolates of spp., by the CLSI M45 fourth edition workgroup. growth was found to be significantly impacted by the brand of reference Mueller-Hinton broth base, and 14.6% of 117 . tested did not grow in cation-adjusted Mueller-Hinton broth supplemented with 5% lysed horse blood after 44 h incubation at 35°C in 5% CO in any brand. Ampicillin and nitrofurantoin MIC breakpoints were established, and penicillin MIC breakpoints were adjusted, based largely on MIC distributions and pharmacokinetic data. Disk criteria were established for penicillin, ampicillin, vancomycin, nitrofurantoin, ciprofloxacin, levofloxacin, and tetracycline. Disk breakpoints could not be established for cefotaxime, ceftriaxone, or meropenem using standard CLSI disk masses due to large zones of growth inhibition that did not differentiate between MIC values and error rates that far exceeded CLSI standards. Trimethoprim-sulfamethoxazole breakpoints were also not possible to establish due to differences in thymidine content between MIC and disk diffusion testing media, which led to no correlation between MIC values and zones of growth inhibition for this antibiotic. The data summarized herein are the basis for proposed changes to the M45 guideline for spp., which will be published in the fourth edition.
species are an increasingly recognized cause of urinary tract infections and may cause serious infections, including endocarditis. Antimicrobial susceptibility testing (AST) is required for the management of these infections, as species within the genus display resistance to various antimicrobial agents. This study describes the data that informed updates to the Clinical and Laboratory Standards Institute M45 guideline for AST of fastidious or infrequently isolated bacteria. We describe the introduction of new ampicillin and nitrofurantoin breakpoints, updated MIC breakpoints for penicillin, and disk diffusion correlates for penicillin, ampicillin, ciprofloxacin, levofloxacin, nitrofurantoin, and tetracycline.
[细菌名称]属是引起尿道感染的革兰氏阳性菌,偶尔也会引发侵袭性感染。临床和实验室标准协会(CLSI)发布的最低抑菌浓度(MIC)断点值得到了评估,CLSI M45第四版工作组通过检测174株[细菌名称]菌株制定了纸片扩散法标准。发现[细菌名称]的生长受参考Mueller-Hinton肉汤基础培养基品牌的显著影响,在任何品牌的添加5%溶解马血的阳离子调整Mueller-Hinton肉汤中,于35°C、5%二氧化碳环境下孵育44小时后,117株受试菌株中有14.6%未生长。基于MIC分布和药代动力学数据,确定了氨苄西林和呋喃妥因的MIC断点值,并调整了青霉素的MIC断点值。确定了青霉素、氨苄西林、万古霉素、呋喃妥因、环丙沙星、左氧氟沙星和四环素的纸片扩散法标准。由于生长抑制圈过大,无法区分MIC值,且错误率远超CLSI标准,因此使用标准CLSI纸片质量无法确定头孢噻肟、头孢曲松或美罗培南的纸片断点值。由于MIC和纸片扩散法检测培养基中胸苷含量不同,导致该抗生素的MIC值与生长抑制圈之间无相关性,因此也无法确定甲氧苄啶-磺胺甲恶唑的断点值。本文总结的数据是对[细菌名称]属M45指南进行修订的依据,该修订版将在第四版中发布。
[细菌名称]属是越来越被认可的尿路感染病因,可能导致严重感染,包括心内膜炎。由于该属内的细菌对多种抗菌药物耐药,因此这些感染的治疗需要进行抗菌药物敏感性试验(AST)。本研究描述了为更新CLSI M45指南中针对苛养菌或不常分离细菌的AST数据。我们描述了新的氨苄西林和呋喃妥因断点值的引入、青霉素MIC断点值的更新,以及青霉素、氨苄西林、环丙沙星、左氧氟沙星、呋喃妥因和四环素的纸片扩散法相关性。