Molecular Epidemiology and Horizontal Transfer Mechanism of optrA-Carrying Linezolid-Resistant Enterococcus faecalis.

Polish journal of microbiology Pub Date : 2024-09-13 eCollection Date: 2024-09-01 DOI:10.33073/pjm-2024-031
Peini Yang, Jiang Li, Mei Lv, Pingan He, Guibo Song, Bin Shan, Xu Yang
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Abstract

The aim of this work was to provide a theoretical and scientific basis for the treatment, prevention, and control of clinical drug-resistant bacterial infections by studying the molecular epidemiology and horizontal transfer mechanism of optrA-carrying linezolid-resistant Enterococcus faecalis strains (LREfs) that were clinically isolated in a tertiary hospital in Kunming, China. Non-repetitive LREfs retained in a tertiary A hospital in Kunming, China. The strains were identified by Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The transferability and horizontal transfer mechanism of optrA gene were analyzed using polymerase chain reaction (PCR), whole-genome sequencing (WGS), and conjugation experiments. A total of 39 LREfs strains were collected, and all of them were multi-drug resistant. There were 30 LREfs strains (76.9%) carrying the optrA gene, The cfr, poxtA genes and mutations in the 23S rRNA gene were not detected. The conjugation experiments showed that only three of 10 randomly selected optrA-carrying LREfs were successfully conjugated with JH2-2. Further analysis of one successfully conjugated strain revealed that the optrA gene, located in the donor bacterium, formed the IS1216E-erm(A)-optrA-fexA-IS1216E transferable fragment under the mediation of the mobile genetic element (MGE) IS1216E, which was then transferred to the recipient bacterium via horizontal plasmid transfer. Carrying the optrA gene is the primary resistance mechanism of LREfs strains. The optrA gene could carry the erm(A) and fexA genes to co-transfer among E. faecalis. MGEs such as insertion sequence IS1216E play an important role in the horizontal transfer of the optrA gene.

携带 optrA 的耐利奈唑胺肠球菌的分子流行病学和水平转移机制。
本研究旨在通过研究中国昆明某三级甲等医院临床分离的携带 optrA 的耐利奈唑胺肠球菌菌株(LREfs)的分子流行病学和水平转移机制,为临床耐药细菌感染的治疗、预防和控制提供理论和科学依据。中国昆明一家三级甲等医院保留的非重复性 LREfs。这些菌株通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)进行鉴定。利用聚合酶链式反应(PCR)、全基因组测序(WGS)和连接实验分析了 optrA 基因的转移性和水平转移机制。共收集到 39 株 LREfs 菌株,它们都具有多重耐药性。其中 30 株 LREfs(76.9%)携带 optrA 基因,未检测到 cfr、poxtA 基因和 23S rRNA 基因突变。共轭实验表明,在随机抽取的 10 株携带 optrA 基因的 LREfs 菌株中,只有 3 株成功与 JH2-2 共轭。对一株成功连接的菌株的进一步分析表明,位于供体细菌中的 optrA 基因在移动遗传因子(MGE)IS1216E 的介导下形成了 IS1216E-erm(A)-optrA-fexA-IS1216E 可转移片段,然后通过水平质粒转移转移到受体细菌中。携带 optrA 基因是 LREfs 菌株的主要抗性机制。optrA 基因可携带 erm(A) 和 fexA 基因,在粪肠球菌中共同转移。插入序列 IS1216E 等 MGE 在 optrA 基因的水平转移中发挥了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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