Comparative phylogenomics of Clostridium difficile reveals clade specificity and microevolution of hypervirulent strains

被引:161
作者
Stabler, R. A.
Gerding, D. N.
Songer, J. G.
Drudy, D.
Brazier, J. S.
Trinh, H. T.
Witney, A. A.
Hinds, J.
Wren, B. W.
机构
[1] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
[2] Loyola Univ, Stritch Sch Med, Hines, IL 60141 USA
[3] Vet Affairs Edward Hines Jr Hosp, Dept Med, Infect Dis Sect, Hines, IL 60141 USA
[4] Vet Affairs Edward Hines Jr Hosp, Dept Med, Res Serv, Hines, IL 60141 USA
[5] Univ Arizona, Dept Vet Sci & Microbiol, Tucson, AZ 85721 USA
[6] Univ Coll Dublin, Ctr Food Safety, Dublin 4, Ireland
[7] Univ Wales Hosp, Anaerobe Reference Lab, NPHS Microbiol Cardiff, Cardiff CF14 4XW, Wales
[8] Univ London, Dept Cellular & Mol Med, Bacterial Microarray Grp, London SW17 0RE, England
基金
英国惠康基金;
关键词
TOXIN PRODUCTION; DIARRHEA; EPIDEMIC; OUTBREAK; DISEASE;
D O I
10.1128/JB.00664-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
\Clostridium difficile is the most frequent cause of nosocomial diarrhea worldwide, and recent reports suggested the emergence of a hypervirulent strain in North America and Europe. In this study, we applied comparative phylogenomics (whole-genome comparisons using DNA microarrays combined with Bayesian phylogenies) to model the phylogeny of C difficile, including 75 diverse isolates comprising hypervirullent, toxin-variable, and animal strains. The analysis identified four distinct statistically supported clusters comprising a hypervirulent clade, a toxin A(-) B+ clade, and two clades with human and animal isolates. Genetic differences among clades revealed several genetic islands relating to virulence and niche adaptation, including antibiotic resistance, motility, adhesion, and enteric metabolism. Only 19.7% of genes were shared by all strains, confirming that this enteric species readily undergoes genetic exchange. This study has provided insight into the possible origins of C. difficile and its evolution that may have implications in disease control strategies.
引用
收藏
页码:7297 / 7305
页数:9
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