Comparative Analysis of the First Complete Enterococcus faecium Genome

被引:111
|
作者
Lam, Margaret M. C. [1 ,6 ]
Seemann, Torsten [2 ]
Bulach, Dieter M. [2 ]
Gladman, Simon L. [3 ]
Chen, Honglei [4 ]
Haring, Volker [4 ]
Moore, Robert J. [4 ,5 ]
Ballard, Susan [6 ]
Grayson, M. Lindsay [6 ,7 ]
Johnson, Paul D. R. [1 ,6 ]
Howden, Benjamin P. [1 ,6 ,8 ,9 ]
Stinear, Timothy P. [1 ,9 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Vic 3010, Australia
[2] Monash Univ, Victorian Bioinformat Consortium, Clayton, Vic, Australia
[3] CSIRO Food & Nutr Sci, Werribee, Vic, Australia
[4] CSIRO, Australian Anim Hlth Lab, Geelong, Vic, Australia
[5] ARC Ctr Excellence Struct & Funct Microbial Genom, Clayton, Vic, Australia
[6] Austin Hlth, Dept Infect Dis, ACIR, Heidelberg, Vic, Australia
[7] Univ Melbourne, Dept Med, Heidelberg, Vic, Australia
[8] Austin Hlth, Dept Microbiol, Heidelberg, Vic, Australia
[9] Monash Univ, Dept Microbiol, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
VANCOMYCIN-RESISTANT ENTEROCOCCI; PROVIDES ACQUIRED-RESISTANCE; SURFACE PROTEIN ESP; INTESTINAL COLONIZATION; PATHOGENICITY ISLAND; GENE; VIRULENCE; EMERGENCE; FAECALIS; MICE;
D O I
10.1128/JB.00259-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vancomycin-resistant enterococci (VRE) are one of the leading causes of nosocomial infections in health care facilities around the globe. In particular, infections caused by vancomycin-resistant Enterococcus faecium are becoming increasingly common. Comparative and functional genomic studies of E. faecium isolates have so far been limited owing to the lack of a fully assembled E. faecium genome sequence. Here we address this issue and report the complete 3.0-Mb genome sequence of the multilocus sequence type 17 vancomycin-resistant Enterococcus faecium strain Aus0004, isolated from the bloodstream of a patient in Melbourne, Australia, in 1998. The genome comprises a 2.9-Mb circular chromosome and three circular plasmids. The chromosome harbors putative E. faecium virulence factors such as enterococcal surface protein, hemolysin, and collagen-binding adhesin. Aus0004 has a very large accessory genome (38%) that includes three prophage and two genomic islands absent among 22 other E. faecium genomes. One of the prophage was present as inverted 50-kb repeats that appear to have facilitated a 683-kb chromosomal inversion across the replication terminus, resulting in a striking replichore imbalance. Other distinctive features include 76 insertion sequence elements and a single chromosomal copy of Tn1549 containing the vanB vancomycin resistance element. A complete E. faecium genome will be a useful resource to assist our understanding of this emerging nosocomial pathogen.
引用
收藏
页码:2334 / 2341
页数:8
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