日本利奈唑胺耐药菌临床分离株的耐药机制及药敏。

IF 3.3 Q2 INFECTIOUS DISEASES
JAC-Antimicrobial Resistance Pub Date : 2025-06-03 eCollection Date: 2025-06-01 DOI:10.1093/jacamr/dlaf097
Ryosuke Shoji, Masayuki Maeda, Kozue Yamaguchi, Takahiro Takuma, Rintaro On, Kazuhisa Ugajin, Daisuke Okatomi, Kunihiko Fukuchi, Issei Tokimatsu, Keiko Ishino
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引用次数: 0

摘要

目的:结合利奈唑胺耐药机制和临床耐药菌株对泰地唑胺敏感性的研究很少。本研究对日本临床分离的利奈唑胺耐药菌株的耐药机制和药敏性进行了研究。方法:对2015 - 2021年日本医院分离的25株耐利奈唑胺的屎肠球菌和粪肠球菌进行分析。采用琼脂平板稀释法测定利奈唑胺和泰地唑胺的mic。每个23S rRNA拷贝通过PCR扩增,测序并分析突变。PCR法检测利奈唑胺耐药基因cfr、poxtA、optrA、fexA和fexB。结果:5株耐利奈唑胺粪肠球菌药敏试验结果显示耐利奈唑胺粪肠球菌药敏浓度低(≤1 mg/L)。耐药机制包括23S rRNA中的G2576T突变、T2504A突变以及耐药基因optrA、fexA和fexB。在一株粪肠杆菌分离株中鉴定出T2504A突变,该菌株的利奈唑胺和泰地唑胺的mic分别为64和32 mg/L。结论:一些耐利奈唑胺的分离株表现出低(≤1 mg/L)的耐利奈唑胺mic。为确定是否应对耐利奈唑胺的分离株进行替地唑胺药敏试验,应收集更多的耐利奈唑胺分离株并进行替地唑胺中等浓度检测。替地唑胺类药物比利奈唑胺类药物低2-3倍稀释度。本研究结果表明,未来的研究应进一步探讨T2504A突变是否有助于抗甾类药物的耐药性。据我们所知,这是首次报道携带T2504A突变的粪肠杆菌和携带该突变的分离株对二唑类药物敏感的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resistance mechanisms and tedizolid susceptibility in clinical isolates of linezolid-resistant bacteria in Japan.

Objectives: Studies combining linezolid resistance mechanisms and tedizolid susceptibility in linezolid-resistant clinical isolates are scarce. This study investigated the linezolid resistance mechanisms and tedizolid susceptibility of linezolid-resistant strains isolated clinically in Japan.

Methods: We analysed 25 linezolid-resistant strains of Enterococcus faecium and Enterococcus faecalis isolated from Japanese hospitals between 2015 and 2021. MICs of linezolid and tedizolid were determined using the agar plate dilution method. Each 23S rRNA copy was amplified by PCR, sequenced and analysed for mutations. The linezolid resistance genes cfr, poxtA, optrA, fexA and fexB were also detected by PCR.

Results: Drug susceptibility tests revealed that five linezolid-resistant E. faecium isolates had low (≤1 mg/L) tedizolid MICs. Resistance mechanisms included the G2576T mutation in 23S rRNA, the T2504A mutation and the resistance genes optrA, fexA and fexB. The T2504A mutation was identified in one E. faecium isolate, which exhibited linezolid and tedizolid MICs of 64 and 32 mg/L, respectively.

Conclusions: Some linezolid-resistant isolates demonstrated low (≤1 mg/L) tedizolid MICs. To determine whether tedizolid susceptibility testing should be performed on linezolid-resistant isolates, more linezolid-resistant isolates should be collected and tested for tedizolid MICs. Tedizolid MICs were 2-3 doubling dilutions lower than linezolid MICs. The results of this study suggest that future research should investigate whether the T2504A mutation contributes to tedizolid resistance. To our knowledge, this is the first study to report tedizolid susceptibility in E. faecium with the T2504A mutation and in isolate harbouring this mutation.

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