Evolutionary dynamics of <i>Clostridium difficile</i> over short and long time scales

Miao He(Wellcome Sanger Institute), Mohammed Sebaihia(Wellcome Sanger Institute), Trevor D. Lawley(Wellcome Sanger Institute), Richard A. Stabler(University of London), Lisa F. Dawson(University of London), Melissa J. Martin(University of London), Kathryn E. Holt(Wellcome Sanger Institute), Helena M. B. Seth-Smith(Wellcome Sanger Institute), Michael A. Quail(Wellcome Sanger Institute), Richard Rance(Wellcome Sanger Institute), Karen Brooks(Wellcome Sanger Institute), Carol Churcher(Wellcome Sanger Institute), David Harris(Wellcome Sanger Institute), Stephen D. Bentley(Wellcome Sanger Institute), Christine Burrows(Wellcome Sanger Institute), Louise Clark(Wellcome Sanger Institute), Craig Corton(Wellcome Sanger Institute), Vicky Murray(Wellcome Sanger Institute), Graham Rose(Wellcome Sanger Institute), Scott Thurston(Wellcome Sanger Institute), Andries J. van Tonder(Wellcome Sanger Institute), Danielle Walker(Wellcome Sanger Institute), Brendan W. Wren(University of London), Gordon Dougan(Wellcome Sanger Institute), Julian Parkhill(Wellcome Sanger Institute)
Proceedings of the National Academy of Sciences
April 5, 2010
Cited by 380Open Access
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Abstract

Clostridium difficile has rapidly emerged as the leading cause of antibiotic-associated diarrheal disease, with the transcontinental spread of various PCR ribotypes, including 001, 017, 027 and 078. However, the genetic basis for the emergence of C. difficile as a human pathogen is unclear. Whole genome sequencing was used to analyze genetic variation and virulence of a diverse collection of thirty C. difficile isolates, to determine both macro and microevolution of the species. Horizontal gene transfer and large-scale recombination of core genes has shaped the C. difficile genome over both short and long time scales. Phylogenetic analysis demonstrates C. difficile is a genetically diverse species, which has evolved within the last 1.1-85 million years. By contrast, the disease-causing isolates have arisen from multiple lineages, suggesting that virulence evolved independently in the highly epidemic lineages.


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