Genome sequence of enterohaemorrhagic Escherichia coli O157:H7

被引:0
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作者
Nicole T. Perna
Guy Plunkett
Valerie Burland
Bob Mau
Jeremy D. Glasner
Debra J. Rose
George F. Mayhew
Peter S. Evans
Jason Gregor
Heather A. Kirkpatrick
György Pósfai
Jeremiah Hackett
Sara Klink
Adam Boutin
Ying Shao
Leslie Miller
Erik J. Grotbeck
N. Wayne Davis
Alex Lim
Eileen T. Dimalanta
Konstantinos D. Potamousis
Jennifer Apodaca
Thomas S. Anantharaman
Jieyi Lin
Galex Yen
David C. Schwartz
Rodney A. Welch
Frederick R. Blattner
机构
[1] Genome Center of Wisconsin,Department of Medical Microbiology and Immunology
[2] ,undefined
[3] Department of Animal Health and Biomedical Sciences,undefined
[4] Laboratory of Genetics,undefined
[5] Department of Chemistry,undefined
[6] Department of Biostatistics,undefined
[7] University of Wisconsin,undefined
[8] Institute of Biochemistry,undefined
[9] Biological Research Center,undefined
[10] Cereon Genomics,undefined
[11] LLC,undefined
来源
Nature | 2001年 / 409卷
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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 syndrome1,2. Close to 75,000 cases of O157:H7 infection are now estimated to occur annually in the United States3. 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 find 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.
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页码:529 / 533
页数:4
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