Comparative Genome Analysis and Global Phylogeny of the Toxin Variant Clostridium difficile PCR Ribotype 017 Reveals the Evolution of Two Independent Sublineages

Author:

Cairns M. D.123,Preston M. D.4,Hall C. L.1,Gerding D. N.56,Hawkey P. M.78,Kato H.9,Kim H.10,Kuijper E. J.11,Lawley T. D.12,Pituch H.13,Reid S.14,Kullin B.14,Riley T. V.15,Solomon K.1617,Tsai P. J.1819,Weese J. S.20,Stabler R. A.1ORCID,Wren B. W.1

Affiliation:

1. Department of Pathogen Molecular Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom

2. UCL Centre for Clinical Microbiology, University College London, Royal Free Campus, London, United Kingdom

3. Public Health Laboratory London, Division of Infection, The Royal London Hospital, London, United Kingdom

4. National Institute for Biological Standards and Control, South Mimms, United Kingdom

5. Edward Hines, Jr., Veterans Affairs Hospital, Hines, Illinois, USA

6. Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA

7. Institute of Microbiology and Infection, University of Birmingham, Edgbaston Campus, Birmingham, United Kingdom

8. Public Health England (PHE), Public Health Laboratory Birmingham (PHLB), Birmingham Heartlands Hospital, Heart of England NHS Foundation Trust, Bordesley Green East, Birmingham, United Kingdom

9. Department of Bacteriology II, National Institute of Infectious Diseases, Tokyo, Japan

10. Department of Laboratory Medicine and Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, South Korea

11. National Reference Laboratory for Clostridium difficile, Leiden University Medical Centre and RIVM, Bilthoven, The Netherlands

12. Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom

13. Department of Medical Microbiology, Medical University of Warsaw, Warsaw, Poland

14. Department of Molecular and Cell Biology, University of Cape Town, Rondebosch, South Africa

15. The University of Western Australia, School of Pathology and Laboratory Medicine, Crawley, Australia

16. School of Medicine and Medical Science, UCD Veterinary Sciences Centre, University College Dublin, Belfield, Dublin, Ireland

17. University of Exeter, Bioscience, College of Life and Environmental Science, Exeter, United Kingdom

18. Department of Medical Laboratory Science and Biotechnology, National Cheng Kung University, Medical College, Tainan, Taiwan

19. Center of Infectious Disease and Signaling Research, National Cheng Kung University, Tainan, Taiwan

20. Department of Pathobiology, University of Guelph, Guelph, Ontario, Canada

Abstract

ABSTRACT The diarrheal pathogen Clostridium difficile consists of at least six distinct evolutionary lineages. The RT017 lineage is anomalous, as strains only express toxin B, compared to strains from other lineages that produce toxins A and B and, occasionally, binary toxin. Historically, RT017 initially was reported in Asia but now has been reported worldwide. We used whole-genome sequencing and phylogenetic analysis to investigate the patterns of global spread and population structure of 277 RT017 isolates from animal and human origins from six continents, isolated between 1990 and 2013. We reveal two distinct evenly split sublineages (SL1 and SL2) of C. difficile RT017 that contain multiple independent clonal expansions. All 24 animal isolates were contained within SL1 along with human isolates, suggesting potential transmission between animals and humans. Genetic analyses revealed an overrepresentation of antibiotic resistance genes. Phylogeographic analyses show a North American origin for RT017, as has been found for the recently emerged epidemic RT027 lineage. Despite having only one toxin, RT017 strains have evolved in parallel from at least two independent sources and can readily transmit between continents.

Funder

DH | National Institute for Health Research

RCUK | Medical Research Council

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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