The Pangenome Structure of<i>Escherichia coli</i>: Comparative Genomic Analysis of<i>E. coli</i>Commensal and Pathogenic Isolates
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- David A. Rasko
- Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201
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- M. J. Rosovitz
- J. Craig Venter Institute, 9712 Medical Center Drive, Rockville, Maryland 20850
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- Garry S. A. Myers
- Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201
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- Emmanuel F. Mongodin
- Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201
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- W. Florian Fricke
- Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201
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- Pawel Gajer
- Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201
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- Jonathan Crabtree
- J. Craig Venter Institute, 9712 Medical Center Drive, Rockville, Maryland 20850
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- Mohammed Sebaihia
- The Wellcome Trust Sanger Institute, Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom
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- Nicholas R. Thomson
- The Wellcome Trust Sanger Institute, Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom
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- Roy Chaudhuri
- Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, United Kingdom
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- Ian R. Henderson
- University of Birmingham, Birmingham, B15 2TT, United Kingdom
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- Vanessa Sperandio
- Department of Microbiology, University of Texas Southwestern Medical Center at Dallas, 6000 Harry Hines Blvd., Dallas, Texas 75235
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- Jacques Ravel
- Institute for Genome Sciences, Department of Microbiology & Immunology, University of Maryland School of Medicine, 20 Penn Street, Baltimore, Maryland 21201
書誌事項
- 公開日
- 2008-10-15
- 権利情報
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- https://journals.asm.org/non-commercial-tdm-license
- DOI
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- 10.1128/jb.00619-08
- 公開者
- American Society for Microbiology
この論文をさがす
説明
<jats:title>ABSTRACT</jats:title><jats:p>Whole-genome sequencing has been skewed toward bacterial pathogens as a consequence of the prioritization of medical and veterinary diseases. However, it is becoming clear that in order to accurately measure genetic variation within and between pathogenic groups, multiple isolates, as well as commensal species, must be sequenced. This study examined the pangenomic content of<jats:italic>Escherichia coli</jats:italic>. Six distinct<jats:italic>E. coli</jats:italic>pathovars can be distinguished using molecular or phenotypic markers, but only two of the six pathovars have been subjected to any genome sequencing previously. Thus, this report provides a seminal description of the genomic contents and unique features of three unsequenced pathovars, enterotoxigenic<jats:italic>E. coli</jats:italic>, enteropathogenic<jats:italic>E. coli</jats:italic>, and enteroaggregative<jats:italic>E. coli</jats:italic>. We also determined the first genome sequence of a human commensal<jats:italic>E. coli</jats:italic>isolate,<jats:italic>E. coli</jats:italic>HS, which will undoubtedly provide a new baseline from which workers can examine the evolution of pathogenic<jats:italic>E. coli</jats:italic>. Comparison of 17<jats:italic>E. coli</jats:italic>genomes, 8 of which are new, resulted in identification of ∼2,200 genes conserved in all isolates. We were also able to identify genes that were isolate and pathovar specific. Fewer pathovar-specific genes were identified than anticipated, suggesting that each isolate may have independently developed virulence capabilities. Pangenome calculations indicate that<jats:italic>E. coli</jats:italic>genomic diversity represents an open pangenome model containing a reservoir of more than 13,000 genes, many of which may be uncharacterized but important virulence factors. This comparative study of the species<jats:italic>E. coli</jats:italic>, while descriptive, should provide the basis for future functional work on this important group of pathogens.</jats:p>
収録刊行物
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- Journal of Bacteriology
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Journal of Bacteriology 190 (20), 6881-6893, 2008-10-15
American Society for Microbiology

