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美国和巴基斯坦屎肠球菌中利奈唑胺耐药表型和基因型特征。

Phenotypic and genotypic characterization of linezolid-resistant Enterococcus faecium from the USA and Pakistan.

机构信息

The Edison Family Center for Genome Sciences & Systems Biology, Washington University in St Louis School of Medicine, St Louis, MO, USA.

Atta ur Rahman School of Applied Biosciences, National University of Sciences and Technology, Islamabad, Pakistan.

出版信息

J Antimicrob Chemother. 2019 Dec 1;74(12):3445-3452. doi: 10.1093/jac/dkz367.

Abstract

OBJECTIVES

Linezolid is an important therapeutic option for the treatment of infections caused by VRE. Linezolid is a synthetic antimicrobial and resistance to this antimicrobial agent remains relatively rare. As a result, data on the comparative genomics of linezolid resistance determinants in Enterococcus faecium are relatively sparse.

METHODS

To address this knowledge gap in E. faecium, we deployed phenotypic antibiotic susceptibility testing and Illumina WGS on hospital surface (environmental) and clinical isolates from the USA and Pakistan.

RESULTS

We found complete concordance between isolate source country and mechanism of linezolid resistance, with all the US isolates possessing a 23S rRNA gene mutation and the Pakistan isolates harbouring two to three acquired antibiotic resistance genes. These resistance genes include the recently elucidated efflux-pump genes optrA and poxtA and a novel cfr-like variant. Although there was no difference in the linezolid MIC between the US and Pakistan isolates, there was a significant difference in the geometric mean of the MIC between the Pakistan isolates that had two versus three of the acquired antibiotic resistance genes. In five of the Pakistan E. faecium that possessed all three of the resistance genes, we found no difference in the local genetic context of poxtA and the cfr-like gene, but we identified different genetic contexts surrounding optrA.

CONCLUSIONS

These results demonstrate that E. faecium from different geographical regions employ alternative strategies to counter selective pressure of increasing clinical linezolid use.

摘要

目的

利奈唑胺是治疗 VRE 感染的重要治疗选择。利奈唑胺是一种合成抗菌药物,对这种抗菌药物的耐药性相对较少。因此,关于粪肠球菌中利奈唑胺耐药决定因素的比较基因组学数据相对较少。

方法

为了填补粪肠球菌中这一知识空白,我们对来自美国和巴基斯坦的医院表面(环境)和临床分离株进行了表型抗生素药敏试验和 Illumina WGS。

结果

我们发现分离株来源国和利奈唑胺耐药机制之间完全一致,所有美国分离株均携带 23S rRNA 基因突变,而巴基斯坦分离株则携带 2 到 3 个获得性抗生素耐药基因。这些耐药基因包括最近阐明的外排泵基因 optrA 和 poxtA 以及一种新型 cfr 样变体。尽管美国和巴基斯坦分离株的利奈唑胺 MIC 之间没有差异,但具有 2 个和 3 个获得性抗生素耐药基因的巴基斯坦分离株的 MIC 几何平均值有显著差异。在携带所有 3 个耐药基因的 5 株巴基斯坦粪肠球菌中,我们发现 poxtA 和 cfr 样基因的局部遗传背景没有差异,但我们发现 optrA 周围的遗传背景不同。

结论

这些结果表明,来自不同地理区域的粪肠球菌采用替代策略来应对临床利奈唑胺使用不断增加的选择压力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b0a/6857194/e943f19449fb/dkz367f1.jpg

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