Genome sequence of enterohaemorrhagic Escherichia coli O157:H7

被引:1554
作者
Perna, NT [1 ]
Plunkett, G
Burland, V
Mau, B
Glasner, JD
Rose, DJ
Mayhew, GF
Evans, PS
Gregor, J
Kirkpatrick, HA
Pósfai, G
Hackett, J
Klink, S
Boutin, A
Shao, Y
Miller, L
Grotbeck, EJ
Davis, NW
Limk, A
Dimalanta, ET
Potamousis, KD
Apodaca, J
Anantharaman, TS
Lin, JY
Yen, G
Schwartz, DC
Welch, RA
Blattner, FR
机构
[1] Univ Wisconsin, Genome Ctr Wisconsin, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Anim Hlth & Biomed Sci, Madison, WI 53706 USA
[3] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[5] Univ Wisconsin, Dept Biostat, Madison, WI 53706 USA
[6] Univ Wisconsin, Dept Med Microbiol & Immunol, Madison, WI 53706 USA
[7] Cereon Genom LLC, Cambridge, MA 02139 USA
[8] Biol Res Ctr, Inst Biochem, H-6701 Szeged, Hungary
关键词
D O I
10.1038/35054089
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The bacterium Escherichia coli O157:H7 is a worldwide threat to public health and has been implicated in many outbreaks of haemorrhagic colitis, some of which included fatalities caused by haemolytic uraemic syndrome(1,2). Close to 75,000 cases of O157:H7 infection are now estimated to occur annually in the United States(3). The severity of disease, the lack of effective treatment and the potential for large-scale outbreaks from contaminated food supplies have propelled intensive research on the pathogenesis and detection of E. coli O157:H7 (ref. 4). Here we have sequenced the genome of E. coli O157:H7 to identify candidate genes responsible for pathogenesis, to develop better methods of strain detection and to advance our understanding of the evolution of E. coli, through comparison with the genome of the non-pathogenic laboratory strain E. coli K-12 (ref. 5). We rnd that lateral gene transfer is far more extensive than previously anticipated. In fact, 1,387 new genes encoded in strain-specific clusters of diverse sizes were found in O157:H7. These include candidate virulence factors, alternative metabolic capacities, several prophages and other new functions-all of which could be targets for surveillance.
引用
收藏
页码:529 / 533
页数:7
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