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粪肠球菌致病岛编码的毒力基因的水平转移。

Horizontal transfer of virulence genes encoded on the Enterococcus faecalis pathogenicity island.

作者信息

Coburn Phillip S, Baghdayan Arto S, Dolan G T, Shankar Nathan

机构信息

Department of Pharmaceutical Sciences, The University of Oklahoma Health Sciences, Center, PO Box 26901, Oklahoma City, OK 73190, USA.

出版信息

Mol Microbiol. 2007 Jan;63(2):530-44. doi: 10.1111/j.1365-2958.2006.05520.x. Epub 2006 Dec 5.

DOI:10.1111/j.1365-2958.2006.05520.x
PMID:17163979
Abstract

Enterococcus faecalis, a leading cause of nosocomial antibiotic resistant infections, frequently possesses a 150 kb pathogenicity island (PAI) that carries virulence determinants. The presence of excisionase and integrase genes, conjugative functions and multiple insertion sequence elements suggests that the PAI, or segments thereof, might be capable of horizontal transfer. In this report, the transfer of the E. faecalis PAI is demonstrated and a mechanism for transfer elucidated. In filter matings, chloramphenicol resistance was observed to transfer from strain MMH594b, a clinical isolate possessing the PAI tagged with a cat marker, to OG1RF (pCGC) with a frequency of 3.2 x 10(-10) per donor. Secondary transfer from primary transconjugant TCRFB1 to strain JH2SS in filter and broth matings occurred with a frequency of 1 and 2 x 10(-1) per donor respectively. Analysis of the transconjugants demonstrated that a 27,744 bp internal PAI segment was capable of excision and circularization in the donor, and is mobilized as a cointegrate with a pTEF1-like plasmid. High-frequency transfer also occurred from TCRFB1 to JH2SS during transient colonization of the mouse gastrointestinal tract. This is the first demonstration of the horizontal transfer of PAI-encoded virulence determinants in E. faecalis and has implications for genome evolution and diversity.

摘要

粪肠球菌是医院获得性抗生素耐药感染的主要原因,通常拥有一个携带毒力决定簇的150 kb致病岛(PAI)。切除酶和整合酶基因的存在、接合功能以及多个插入序列元件表明,PAI或其片段可能能够进行水平转移。在本报告中,证明了粪肠球菌PAI的转移并阐明了转移机制。在滤膜交配实验中,观察到氯霉素抗性从携带用cat标记的PAI的临床分离株MMH594b转移到OG1RF(pCGC),转移频率为每供体3.2×10⁻¹⁰。在滤膜和肉汤交配中,从初级转接合子TCRFB1到菌株JH2SS的二次转移频率分别为每供体1和2×10⁻¹。对转接合子的分析表明,一个27,744 bp的内部PAI片段能够在供体中切除和环化,并作为与pTEF1样质粒的共整合体被转移。在小鼠胃肠道短暂定殖期间,TCRFB1到JH2SS也发生了高频转移。这是首次证明粪肠球菌中PAI编码的毒力决定簇的水平转移,对基因组进化和多样性具有重要意义。

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