TY - JOUR
T1 - Genome sequence of enterohaemorrhagic Escherichia coli O157:H7
AU - Perna, Nicole T.
AU - Plunkett, Guy
AU - Burland, Valerie
AU - Mau, Bob
AU - Glasner, Jeremy D.
AU - Rose, Debra J.
AU - Mayhew, George F.
AU - Evans, Peter S.
AU - Gregor, Jason
AU - Kirkpatrick, Heather A.
AU - Pósfai, György
AU - Hackett, Jeremiah
AU - Klink, Sara
AU - Boutin, Adam
AU - Shao, Ying
AU - Miller, Leslie
AU - Grotbeck, Erik J.
AU - Davis, N. Wayne
AU - Lim, Alex
AU - Dimalanta, Eileen T.
AU - Potamousis, Konstantinos D.
AU - Apodaca, Jennifer
AU - Anantharaman, Thomas S.
AU - Lin, Jieyi
AU - Yen, Galex
AU - Schwartz, David C.
AU - Welch, Rodney A.
AU - Blattner, Frederick R.
PY - 2001/1/25
Y1 - 2001/1/25
N2 - 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 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.
AB - 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 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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U2 - 10.1038/35054089
DO - 10.1038/35054089
M3 - Article
C2 - 11206551
AN - SCOPUS:0035945586
SN - 0028-0836
VL - 409
SP - 529
EP - 533
JO - Nature
JF - Nature
IS - 6819
ER -