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万古霉素耐药金黄色葡萄球菌基因组中 vanA 操纵子获得的机制:冰山一角?

Mechanisms of acquisition of the vanA operon among vancomycin-resistant Staphylococcus aureus genomes: The tip of the iceberg?

机构信息

Aix Marseille University, MEPHI, Marseille, France; Institut Hospitalo-Universitaire (IHU) Méditerranée Infection, Marseille, France.

Aix Marseille University, MEPHI, Marseille, France; Institut Hospitalo-Universitaire (IHU) Méditerranée Infection, Marseille, France; Centre National de la Recherche Scientifique (CNRS)-SNC5039, Marseille, France.

出版信息

Int J Antimicrob Agents. 2024 Jun;63(6):107154. doi: 10.1016/j.ijantimicag.2024.107154. Epub 2024 Apr 9.

Abstract

BACKGROUND

Vancomycin is frequently used as a last line of defence against infections due to multidrug-resistant Staphylococcus aureus (S. aureus). A recent finding described the acquisition of vancomycin-resistant S. aureus strains by the integration of an enterococcal plasmid containing the vanA operon into the S. aureus chromosome via homologous recombination involving a specific integration site called locus L2.

METHODS

To characterise all mechanisms of acquisition of vanA, this study analysed the 15 706 S. aureus genomes to look for vanA and described its genetic environment.

RESULTS

A complete vanA operon was found in 25 S. aureus strains isolated from 12 patients, including nine co-isolated with vancomycin-resistant Enterococcus strains. VanA was found within transposon Tn1546-like elements on 17 plasmids and eight chromosomes. VanA might be acquired through conjugation of enterococcal and staphylococcal plasmids, transposition of Tn1546 carrying vanA and plasmid integration into the chromosome. Further, L2 was detected in 2087 genomes (13.3%) of S. aureus strains across different continents. Six potential chromosomal hotspots for integration of the entire vanA-containing enterococcal plasmid were identified by homologous recombination via L2.

CONCLUSIONS

These findings suggest that the recently described scenario in a New York patient could be reproduced anywhere. Surveillance of this possibility is mandatory, especially in patients with vancomycin-resistant Enterococcus infection or colonisation.

摘要

背景

由于耐多药金黄色葡萄球菌 (S. aureus) 的感染,万古霉素经常被用作最后的防御手段。最近的一项发现描述了通过同源重组将含有 vanA 操纵子的肠球菌质粒整合到 S. aureus 染色体中,涉及特定的整合位点称为 locus L2,从而获得耐万古霉素的 S. aureus 菌株。

方法

为了描述获得 vanA 的所有机制,本研究分析了 15706 株金黄色葡萄球菌基因组,寻找 vanA 并描述其遗传环境。

结果

在 12 名患者分离的 25 株金黄色葡萄球菌中发现了完整的 vanA 操纵子,其中 9 株与耐万古霉素肠球菌同时分离。VanA 位于 17 个质粒和 8 个染色体上的转座子 Tn1546 样元件内。VanA 可能通过肠球菌和葡萄球菌质粒的接合、携带 vanA 的 Tn1546 的转位以及质粒整合到染色体中获得。此外,在来自不同大陆的 2087 株金黄色葡萄球菌基因组(占 13.3%)中检测到 L2。通过 L2 同源重组鉴定了 6 个整合整个含 vanA 肠球菌质粒的潜在染色体热点。

结论

这些发现表明,最近在纽约患者中描述的情况可能在任何地方重现。必须对这种可能性进行监测,尤其是在耐万古霉素肠球菌感染或定植的患者中。

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