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市售培养基对头孢地尔肉汤微量稀释法药敏试验的影响。

The impact of commercially available media on cefiderocol susceptibility testing by broth microdilution method.

作者信息

DeJonge Boudewijn L M, Slover Christine, Nguyen Sean T, Longshaw Christopher, Takemura Miki, Anan Naomi, Yamashiro Hidenori, Yamano Yoshinori

机构信息

Shionogi IncFlorham Park, New Jersey, USA.

Shionogi B.V.London, United Kingdom.

出版信息

J Clin Microbiol. 2025 Sep 10;63(9):e0047125. doi: 10.1128/jcm.00471-25. Epub 2025 Aug 20.

Abstract

The reference method for determining cefiderocol MIC is broth microdilution (BMD) using iron-depleted cation-adjusted Mueller-Hinton broth (ID-CAMHB). However, laboratories have reported variable MIC findings and difficulties in determining MIC endpoints. To investigate this, the BMD method was re-evaluated by examining the chelation time for iron depletion of the media and by testing reproducibility using four MHB sources (BD-BBL, BD-Difco, Oxoid, and Merck) and 85 Gram-negative isolates (, , , and ), of which 63 were previously evaluated . Extending chelation time to 6 h provided optimal iron reduction to ≤0.03 µg/mL for all media. MIC reproducibility was high for each medium source and varied by species (93.3%-99.0% of MIC values within one dilution of modal MIC values); however, different sources of ID-CAMHB produced (reproducible) different modal MIC values for isolates. ID-CAMHB from BD-BBL and BD-Difco showed the best correlation with 96.5% of isolates showing modal MIC values within one dilution between media. MIC values generated with these two media were the most predictive of efficacy . When trailing was observed, it was seen across all media, and refined reading guidelines were applied to enhance reproducibility of determining the MIC endpoint. The 6-h chelation and the refined reading guidelines for trailing are now incorporated into the Clinical and Laboratory Standards Institute M100 document. When using the BMD method to determine cefiderocol susceptibility, the impact of media should be considered, and based on these results, ID-CAMHB prepared with BD-BBL or BD-Difco is recommended.IMPORTANCEThe reference antibiotic susceptibility testing method for cefiderocol is the broth microdilution method approved by the Clinical and Laboratory Standards Institute in 2016, using iron-depleted cation-adjusted Mueller-Hinton broth. A few manual devices have come to the market replicating this method, but inconsistent results with these devices have been reported. The current study identified the source of Mueller-Hinton broth as a variable in cefiderocol MIC determinations and provides detailed description of the preparation of iron-depleted cation-adjusted Mueller-Hinton broth, and revised reading guidance to improve reproducibility of cefiderocol MIC determinations for , , , and . The recommendations made in this study should enhance the reproducibility of cefiderocol broth microdilution susceptibility testing.

摘要

测定头孢地尔最低抑菌浓度(MIC)的参考方法是使用缺铁阳离子调整的穆勒-欣顿肉汤(ID-CAMHB)进行肉汤微量稀释(BMD)。然而,各实验室报告的MIC结果存在差异,且在确定MIC终点时存在困难。为了对此进行研究,通过检查培养基中铁耗尽的螯合时间,并使用四种MHB来源(BD-BBL、BD-Difco、Oxoid和默克)以及85株革兰氏阴性分离株(、、和)测试重现性,对BMD方法进行了重新评估,其中63株先前已评估过。将螯合时间延长至6小时可使所有培养基中的铁最佳还原至≤0.03µg/mL。每种培养基来源的MIC重现性都很高,且因菌种而异(在模式MIC值的一个稀释度内,93.3%-99.0%的MIC值);然而,不同来源的ID-CAMHB对分离株产生了(可重现的)不同模式MIC值。来自BD-BBL和BD-Difco的ID-CAMHB显示出最佳相关性,96.5%的分离株在两种培养基之间的一个稀释度内显示出模式MIC值。用这两种培养基产生的MIC值对疗效的预测性最强。当观察到拖尾现象时,在所有培养基中均可见,并且应用了改进的读数指南以提高确定MIC终点的重现性。6小时螯合和拖尾的改进读数指南现已纳入临床和实验室标准协会M100文件。使用BMD方法测定头孢地尔敏感性时,应考虑培养基的影响,基于这些结果,建议使用BD-BBL或BD-Difco制备的ID-CAMHB。重要性头孢地尔的参考抗生素敏感性测试方法是临床和实验室标准协会于2016年批准的肉汤微量稀释法,使用缺铁阳离子调整的穆勒-欣顿肉汤。一些手动设备已投放市场,可复制此方法,但已报告这些设备的结果不一致。当前研究确定了穆勒-欣顿肉汤的来源是头孢地尔MIC测定中的一个变量,并详细描述了缺铁阳离子调整的穆勒-欣顿肉汤的制备方法,以及改进的读数指南,以提高对、、和的头孢地尔MIC测定的重现性。本研究提出的建议应可提高头孢地尔肉汤微量稀释敏感性测试的重现性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1fc/12421808/7f66703221af/jcm.00471-25.f001.jpg

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