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替加环素对 43 种诺卡氏菌属种属的体外活性。

In vitro activity of tedizolid against 43 species of Nocardia species.

机构信息

Department of Clinical Laboratory Sciences, School of Health Sciences, Fukushima Medical University, Fukushima, 10-6, Sakaemachi, Fukushima City, Fukushima, 960-8516, Japan.

Department of Laboratory Medicine, Fukushima Medical University, 1 Hikariga-Oka, Fukushima City, Fukushima, 960-1295, Japan.

出版信息

Sci Rep. 2024 Mar 4;14(1):5342. doi: 10.1038/s41598-024-55916-7.

Abstract

The purpose of the present study was to evaluate the in vitro activity of tedizolid against several clinically significant species of Nocardia by comparing with that of linezolid. A total of 286 isolates of Nocardia species, including 236 clinical isolates recovered from patients in Japan and 50 strains (43 species) purchased from NITE Biological Resource Center, were studied. Antimicrobial susceptibility testing was performed using the broth microdilution method. For the 286 Nocardia isolates, the minimal inhibitory concentration (MIC) and MIC values of tedizolid were 0.25 and 0.5 μg/ml, and those of linezolid were 2 and 2 μg/ml, respectively. The distribution of the linezolid/tedizolid ratios (MICs of linezolid/MICs of tedizolid) showed that tedizolid had four- to eight-fold higher activity than linezolid in 96.1% (275/286) of Nocardia isolates. Both the tedizolid and linezolid MIC values for Nocardia brasiliensis were two-fold higher than those for the other Nocardia species. Both tedizolid and linezolid had low MIC values, 0.25-1 μg/ml and 0.5-4 μg/ml, respectively, even against nine isolates (five species) that were resistant to trimethoprim/sulfamethoxazole. One Nocardia sputorum isolate showed reduced susceptibility to tedizolid (4 μg/ml). Bioinformatics analysis suggests different resistance mechanisms than the oxazolidinone resistance seen in enterococci and staphylococci.

摘要

本研究旨在通过比较替加环素与利奈唑胺,评估替加环素对几种临床重要的诺卡氏菌属的体外活性。共研究了 286 株诺卡氏菌属分离株,包括从日本患者中分离的 236 株临床分离株和从 NITE 生物资源中心购买的 50 株(43 种)菌株。采用肉汤微量稀释法进行药敏试验。对于 286 株诺卡氏菌分离株,替加环素的最小抑菌浓度(MIC)和 MIC 值分别为 0.25 和 0.5μg/ml,利奈唑胺的 MIC 值为 2 和 2μg/ml。利奈唑胺/替加环素(利奈唑胺 MIC 值/替加环素 MIC 值)比值的分布表明,替加环素对 96.1%(275/286)的诺卡氏菌分离株的活性比利奈唑胺高 4 至 8 倍。替加环素和利奈唑胺对巴西诺卡氏菌的 MIC 值均比其他诺卡氏菌属的 MIC 值高两倍。替加环素和利奈唑胺的 MIC 值均较低,分别为 0.25-1μg/ml 和 0.5-4μg/ml,即使对 9 株(5 种)对甲氧苄啶/磺胺甲恶唑耐药的分离株也是如此。一株游动放线菌对替加环素的敏感性降低(4μg/ml)。生物信息学分析表明,其耐药机制与肠球菌和葡萄球菌中的唑烷酮类耐药机制不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6000/10912709/618bc77148b6/41598_2024_55916_Fig1_HTML.jpg

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