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耐甲氧西林金黄色葡萄球菌向耐药性增强方向的演变。

Evolution of methicillin-resistant Staphylococcus aureus towards increasing resistance.

作者信息

Strommenger Birgit, Bartels Mette Damkjær, Kurt Kevin, Layer Franziska, Rohde Susanne Mie, Boye Kit, Westh Henrik, Witte Wolfgang, De Lencastre Herminia, Nübel Ulrich

机构信息

National Reference Centre for Staphylococci and Enterococci, Robert Koch Institute, Wernigerode Branch, Wernigerode, Germany.

出版信息

J Antimicrob Chemother. 2014 Mar;69(3):616-22. doi: 10.1093/jac/dkt413. Epub 2013 Oct 22.

Abstract

OBJECTIVES

To elucidate the evolutionary history of Staphylococcus aureus clonal complex (CC) 8, which encompasses several globally distributed epidemic lineages, including hospital-associated methicillin-resistant S. aureus (MRSA) and the highly prevalent community-associated MRSA clone USA300.

METHODS

We reconstructed the phylogeny of S. aureus CC8 by mutation discovery at 112 genetic housekeeping loci from each of 174 isolates, sampled on five continents between 1957 and 2008. The distribution of antimicrobial resistance traits and of diverse mobile genetic elements was investigated in relation to the isolates' phylogeny.

RESULTS

Our analyses revealed the existence of nine phylogenetic clades within CC8. We identified at least eight independent events of methicillin resistance acquisition in CC8 and dated the origin of a methicillin-resistant progenitor of the notorious USA300 clone to the mid-1970s. Of the S. aureus isolates in our collection, 88% carried plasmidic rep gene sequences, with up to five different rep genes in individual isolates and a total of eight rep families. Mapping the plasmid content onto the isolates' phylogeny illustrated the stable carriage over decades of some plasmids and the more volatile nature of others. Strikingly, we observed trends of increasing antibiotic resistance during the evolution of several lineages, including USA300.

CONCLUSIONS

We propose a model for the evolution of S. aureus CC8, involving a split into at least nine phylogenetic lineages and a subsequent series of acquisitions and losses of mobile genetic elements that carry diverse virulence and antimicrobial resistance traits. The evolution of MRSA USA300 towards resistance to additional antibiotic classes is of major concern.

摘要

目的

阐明金黄色葡萄球菌克隆复合体(CC)8的进化史,该复合体包含多个全球分布的流行谱系,包括医院相关的耐甲氧西林金黄色葡萄球菌(MRSA)和高度流行的社区相关MRSA克隆USA300。

方法

我们通过对1957年至2008年间在五大洲采集的174株分离株的112个管家基因座进行突变发现,重建了金黄色葡萄球菌CC8的系统发育。研究了抗菌药物耐药性特征和多种移动遗传元件的分布与分离株系统发育的关系。

结果

我们的分析揭示了CC8内存在九个系统发育分支。我们在CC8中确定了至少八次独立的获得甲氧西林耐药性的事件,并将臭名昭著的USA300克隆的耐甲氧西林祖细胞的起源追溯到20世纪70年代中期。在我们收集的金黄色葡萄球菌分离株中,88%携带质粒rep基因序列,单个分离株中多达五个不同的rep基因,总共八个rep家族。将质粒含量映射到分离株的系统发育上,说明了一些质粒在几十年中的稳定携带以及其他质粒的更易变性质。引人注目的是,我们在包括USA300在内的几个谱系的进化过程中观察到了抗生素耐药性增加的趋势。

结论

我们提出了一个金黄色葡萄球菌CC8的进化模型,包括分裂为至少九个系统发育谱系,以及随后一系列携带不同毒力和抗菌耐药性特征的移动遗传元件的获得和丢失。MRSA USA300对其他抗生素类别的耐药性进化是一个主要问题。

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