4.6 Article

Macro and Micro Diversity of Clostridium difficile Isolates from Diverse Sources and Geographical Locations

Journal

PLOS ONE
Volume 7, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0031559

Keywords

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Funding

  1. Wellcome Trust [086418/Z/]
  2. National Institute for Health Research
  3. Marie Curie Intra-European fellowship [PIEF-GA-2009-252207-CDI]
  4. NIHR Biomedical Research Centre, Oxford, United Kingdom
  5. CSO
  6. Engineering and Physical Sciences Research Council [EP/E500412/1] Funding Source: researchfish
  7. Medical Research Council [G0300020] Funding Source: researchfish
  8. National Institute for Health Research [HCS/D10/020] Funding Source: researchfish
  9. MRC [G0300020] Funding Source: UKRI
  10. National Institutes of Health Research (NIHR) [HCS/D10/020] Funding Source: National Institutes of Health Research (NIHR)

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Clostridium difficile has emerged rapidly as the leading cause of antibiotic-associated diarrheal disease, with the temporal and geographical appearance of dominant PCR ribotypes such as 017, 027 and 078. Despite this continued threat, we have a poor understanding of how or why particular variants emerge and the sources of strains that dominate different human populations. We have undertaken a breadth genotyping study using multilocus sequence typing (MLST) analysis of 385 C. difficile strains from diverse sources by host (human, animal and food), geographical locations (North America, Europe and Australia) and PCR ribotypes. Results identified 18 novel sequence types (STs) and 3 new allele sequences and confirmed the presence of five distinct clonal lineages generally associated with outbreaks of C. difficile infection in humans. Strains of animal and food origin were found of both ST-1 and ST-11 that are frequently associated with human disease. An in depth MLST analysis of the evolutionary distant ST-11/PCR ribotype 078 clonal lineage revealed that ST-11 can be found in alternative but closely related PCR ribotypes and PCR ribotype 078 alleles contain mutations generating novel STs. PCR ribotype 027 and 017 lineages may consist of two divergent subclades. Furthermore evidence of microdiversity was present within the heterogeneous clade 1. This study helps to define the evolutionary origin of dominant C. difficile lineages and demonstrates that C. difficile is continuing to evolve in concert with human activity.

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