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不同产毒艰难梭菌 PCR 核糖体分型中甲硝唑药敏分析。

Analysis of metronidazole susceptibility in different Clostridium difficile PCR ribotypes.

机构信息

Department of Infectious, Parasitic and Immune-mediated Diseases, Istituto Superiore di Sanità, Rome, Italy.

出版信息

J Antimicrob Chemother. 2013 Feb;68(2):362-5. doi: 10.1093/jac/dks420. Epub 2012 Oct 26.

DOI:10.1093/jac/dks420
PMID:23104495
Abstract

OBJECTIVES

Susceptibility to metronidazole was investigated in 81 Clostridium difficile strains, belonging to nine different PCR ribotypes, by three different laboratory methods.

METHODS

MICs for 81 C. difficile clinical isolates were determined by Etest, the agar dilution method (ADM) and the agar incorporation method (AIM). Twenty selected strains were also subjected to subinhibitory concentrations of metronidazole and the MIC heterogeneity was analysed in colonies from each strain that showed increased values before and after exposure to the antibiotic, using ADM and AIM.

RESULTS

Overall, the MICs obtained by Etest were lower compared with those obtained by ADM and AIM, causing discrepancies in the categorization (as susceptible or having reduced susceptibility) of some strains. Reduced susceptibility to metronidazole was observed using both ADM and AIM, with higher MIC values by AIM in isolates belonging to PCR ribotypes 001 and 010. An increase in MICs after exposure to metronidazole was observed for strains belonging to these PCR ribotypes (by Etest and ADM, but not by AIM). In particular, MICs for colonies from strains belonging to either PCR ribotype 001 or 010 were less heterogeneous by AIM compared with by ADM, suggesting a better ability of AIM to detect strains with reduced susceptibility.

CONCLUSIONS

These results suggest that the presence of C. difficile subpopulations with reduced susceptibility to metronidazole in the human intestine may be one of the factors responsible for reduced antibiotic efficacy in vivo. The possibility that higher MICs may have often gone unnoticed underlines the importance of choosing the best method for MIC determination and the necessity to monitor C. difficile susceptibility to metronidazole.

摘要

目的

通过三种不同的实验室方法,研究了 81 株属于 9 种不同 PCR 核糖体分型的艰难梭菌对甲硝唑的敏感性。

方法

采用 Etest、琼脂稀释法(ADM)和琼脂掺入法(AIM)测定 81 株艰难梭菌临床分离株的 MIC。还对 20 株选定的菌株进行了亚抑菌浓度的甲硝唑处理,并在暴露于抗生素前后,通过 ADM 和 AIM 分析每个菌株中增加值的菌落,分析 MIC 异质性。

结果

总的来说,Etest 获得的 MICs 低于 ADM 和 AIM 获得的 MICs,导致一些菌株的分类(敏感或敏感性降低)出现差异。ADM 和 AIM 均观察到甲硝唑的敏感性降低,PCR 核糖体分型 001 和 010 的分离株 MIC 值较高。暴露于甲硝唑后,观察到一些菌株的 MIC 值增加(Etest 和 ADM,但 AIM 则没有)。特别是,PCR 核糖体分型 001 或 010 菌株的菌落的 MIC 值通过 AIM 比 ADM 更具有异质性,表明 AIM 更能检测出敏感性降低的菌株。

结论

这些结果表明,人类肠道中存在甲硝唑敏感性降低的艰难梭菌亚群可能是体内抗生素疗效降低的原因之一。较高的 MICs 可能经常被忽视,这突显了选择最佳 MIC 测定方法的重要性,以及监测艰难梭菌对甲硝唑敏感性的必要性。

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