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Emergence and global spread of epidemic healthcare-associated Clostridium difficile

Authors
 Miao He  ;  Fabio Miyajima  ;  Paul Roberts  ;  Louise Ellison  ;  Derek J Pickard  ;  Melissa J Martin  ;  Thomas R Connor  ;  Simon R Harris  ;  Derek Fairley  ;  Kathleen B Bamford  ;  Stephanie D'Arc  ;  Jon Brazier  ;  Derek Brown  ;  John E Coia  ;  Gill Douce  ;  Dale Gerding  ;  Hee Jung Kim  ;  Tse Hsien Koh  ;  Haru Kato  ;  Mitsutoshi Senoh  ;  Tom Louie  ;  Stephen Michell  ;  Emma Butt  ;  Sharon J Peacock  ;  Nick M Brown  ;  Tom Riley  ;  Glen Songer  ;  Mark Wilcox  ;  Munir Pirmohamed  ;  Ed Kuijper  ;  Peter Hawkey  ;  Brendan W Wren  ;  Gordon Dougan  ;  Julian Parkhill  ;  Trevor D Lawley 
Citation
 NATURE GENETICS, Vol.45(1) : 109-155, 2013 
Journal Title
NATURE GENETICS
ISSN
 1061-4036 
Issue Date
2013
MeSH
Clostridium difficile/classification ; Clostridium difficile/genetics* ; Diarrhea/epidemiology* ; Enterocolitis, Pseudomembranous/epidemiology* ; Epidemics ; Genome, Bacterial ; Genotype ; Humans ; Phylogeny ; Phylogeography ; Polymorphism, Single Nucleotide
Keywords
Clostridium difficile/classification ; Clostridium difficile/genetics* ; Diarrhea/epidemiology* ; Enterocolitis, Pseudomembranous/epidemiology* ; Epidemics ; Genome, Bacterial ; Genotype ; Humans ; Phylogeny ; Phylogeography ; Polymorphism, Single Nucleotide
Abstract
Epidemic C. difficile (027/BI/NAP1) has rapidly emerged in the past decade as the leading cause of antibiotic-associated diarrhea worldwide. However, the key events in evolutionary history leading to its emergence and the subsequent patterns of global spread remain unknown. Here, we define the global population structure of C. difficile 027/BI/NAP1 using whole-genome sequencing and phylogenetic analysis. We show that two distinct epidemic lineages, FQR1 and FQR2, not one as previously thought, emerged in North America within a relatively short period after acquiring the same fluoroquinolone resistance-conferring mutation and a highly related conjugative transposon. The two epidemic lineages showed distinct patterns of global spread, and the FQR2 lineage spread more widely, leading to healthcare-associated outbreaks in the UK, continental Europe and Australia. Our analysis identifies key genetic changes linked to the rapid transcontinental dissemination of epidemic C. difficile 027/BI/NAP1 and highlights the routes by which it spreads through the global healthcare system.
Full Text
http://www.nature.com/ng/journal/v45/n1/full/ng.2478.html
DOI
10.1038/ng.2478
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
Yonsei Authors
Kim, Heejung(김희정) ORCID logo https://orcid.org/0000-0002-0190-703X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/86848
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