TY - JOUR
T1 - A Role for Tetracycline Selection in Recent Evolution of Agriculture-Associated Clostridium difficile PCR Ribotype 078
AU - Dingle, Kate E.
AU - Didelot, Xavier
AU - Quan, T. Phuong
AU - Eyre, David W.
AU - Stoesser, Nicole
AU - Marwick, Charis Ann
AU - Coia, John
AU - Brown, Derek
AU - Buchanan, Sarah
AU - Ijaz, Umer Z.
AU - Goswami, Cosmika
AU - Douce, Gill
AU - Fawley, Warren N.
AU - Wilcox, Mark H.
AU - Peto, Timothy E. A.
AU - Walker, A. Sarah
AU - Crook, Derrick W.
N1 - Funding Information:
We thank the Food Animal Initiative in Oxford for access to animals to sample for C. difficile at the Oxford University Farm, Wytham. This project was funded by the National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare Associated Infections and Antimicrobial Resistance at Oxford University in partnership with Public Health England (PHE) (grant HPRU-2012-10041). This study was also supported by OU UKCRC Modernising Medical Microbiology Consortium funded by Medical Research Council, Biotechnology and Biological Sciences Research Council and The National Institute for Health Research on behalf of the Department of Health (Grant G0800778) and the Wellcome Trust (Grant 087646/Z/08/Z); NIHR Oxford Biomedical Research Centre, NIHR Health on Modelling Methodology (grant HPRU-2012-10080), and the Health Innovation Challenge Fund (a parallel funding partnership between the Wellcome Trust [grant WT098615/Z/12/Z] and the Department of Health [grant HICF-T5-358]). The identification, isolation, and anal-ysis of the Scottish RT078 isolates was funded by a Scottish Infection Research Network (SIRN) grant (ref SIRN/09), awarded to G.D. and C.A.M. (principal investigators [PIs]) and to J.C., D.B., and U.Z.I. (coapplicants). K.E.D. was supported by NIHR Oxford Biomedical Research Centre; D.W.C. and T.E.A.P. are NIHR senior investigators. S.B. was supported as a Daphne Jackson Fellow funded by Medical Research Scotland. U.Z.I. was supported by a NERC independent research fellowship (NE/LO11956/1). We acknowledge the contribution of the Modernising Medical Microbiology Informatics Group, comprising the following members: Carlos Del Ojo Elias, Charles Crichton, Vasiliki Kostiou, and Adam Giess (Nuffield Department of Clinical Medicine, University of Oxford, United Kingdom) and Jim Davies (Department of Computer Science, University of Oxford, United Kingdom). The views expressed in this publication are those of the authors and not necessarily those of the funders. K.E.D., X.D., T.E.A.P., A.S.W., and D.W.C. conceived and designed the study; K.E.D., D.W.E., N.S., C.A.M., J.C., D.B., S.B., U.Z.I., C.G., G.D., W.N.F., M.H.W., T.E.A.P., A.S.W., and D.W.C. contributed isolates and DNA sequence data; X.D. and D.W.E. performed phylogenetic analysis; X.D. and D.W.E. provided bioinformatics support; T.P.Q. and A.S.W. performed evolutionary distinctiveness analysis; K.E.D. analyzed DNA sequence data for antimicrobial resistance determinants; K.E.D., X.D., D.W.E., M.H.W., T.E.A.P., A.S.W., and D.W.C. wrote the manuscript. All of us reviewed the manuscript and approved it for submission. M.H.W. has received consulting fees from Abbott Laboratories, Actelion, Aicuris, Astellas, Astra-Zeneca, Bayer, bioMérieux, Cambimune, Cerexa, Da Volterra, The European Tissue Symposium, The Medicines Company, MedImmune, Menarini, Merck, Meridian, Motif Biosciences, Nabriva, Paratek, Pfizer, Qiagen, Roche, Sanofi-Pasteur, Seres, Summit, Synthetic Biologics, and Valneva; lecture fees from Abbott, Alere, Allergan, Astellas, Astra-Zeneca, Merck, Pfizer, Roche, and Seres; and grant support from Abbott, Actelion, Astellas, bioMérieux, Cubist, Da Volterra, MicroPharm, Morphochem AG, Sanofi-Pasteur, Seres, Summit, The European Tissue Symposium, and Merck. The rest of us declare that we have no competing financial interests.
Publisher Copyright:
© 2019 Dingle et al.
PY - 2019/4
Y1 - 2019/4
N2 - The increasing clinical importance of human infections (frequently severe) caused by Clostridium difficile PCR ribotype 078 (RT078) was first reported in 2008. The severity of symptoms (mortality of ≤30%) and the higher proportion of infections among community and younger patients raised concerns. Farm animals, especially pigs, have been identified as RT078 reservoirs. We aimed to understand the recent changes in RT078 epidemiology by investigating a possible role for antimicrobial selection in its recent evolutionary history. Phylogenetic analysis of international RT078 genomes (isolates from 2006 to 2014, n = 400), using time-scaled, recombination-corrected, maximum likelihood phylogenies, revealed several recent clonal expansions. A common ancestor of each expansion had independently acquired a different allele of the tetracycline resistance gene tetM Consequently, an unusually high proportion (76.5%) of RT078 genomes were tetM positive. Multiple additional tetracycline resistance determinants were also identified (including efflux pump tet40), frequently sharing a high level of nucleotide sequence identity (up to 100%) with sequences found in the pig pathogen Streptococcus suis and in other zoonotic pathogens such as Campylobacter jejuni and Campylobacter coli Each RT078 tetM clonal expansion lacked geographic structure, indicating rapid, recent international spread. Resistance determinants for C. difficile infection-triggering antimicrobials, including fluoroquinolones and clindamycin, were comparatively rare in RT078. Tetracyclines are used intensively in agriculture; this selective pressure, plus rapid, international spread via the food chain, may explain the increased RT078 prevalence in humans. Our work indicates that the use of antimicrobials outside the health care environment has selected for resistant organisms, and in the case of RT078, has contributed to the emergence of a human pathogen.IMPORTANCEClostridium difficile PCR ribotype 078 (RT078) has multiple reservoirs; many are agricultural. Since 2005, this genotype has been increasingly associated with human infections in both clinical settings and the community. Investigations of RT078 whole-genome sequences revealed that tetracycline resistance had been acquired on multiple independent occasions. Phylogenetic analysis revealed a rapid, recent increase in numbers of closely related tetracycline-resistant RT078 (clonal expansions), suggesting that tetracycline selection has strongly influenced its recent evolutionary history. We demonstrate recent international spread of emergent, tetracycline-resistant RT078. A similar tetracycline-positive clonal expansion was also identified in unrelated nontoxigenic C. difficile, suggesting that this process may be widespread and may be independent of disease-causing ability. Resistance to typical C. difficile infection-associated antimicrobials (e.g., fluoroquinolones, clindamycin) occurred only sporadically within RT078. Selective pressure from tetracycline appears to be a key factor in the emergence of this human pathogen and the rapid international dissemination that followed, plausibly via the food chain.
AB - The increasing clinical importance of human infections (frequently severe) caused by Clostridium difficile PCR ribotype 078 (RT078) was first reported in 2008. The severity of symptoms (mortality of ≤30%) and the higher proportion of infections among community and younger patients raised concerns. Farm animals, especially pigs, have been identified as RT078 reservoirs. We aimed to understand the recent changes in RT078 epidemiology by investigating a possible role for antimicrobial selection in its recent evolutionary history. Phylogenetic analysis of international RT078 genomes (isolates from 2006 to 2014, n = 400), using time-scaled, recombination-corrected, maximum likelihood phylogenies, revealed several recent clonal expansions. A common ancestor of each expansion had independently acquired a different allele of the tetracycline resistance gene tetM Consequently, an unusually high proportion (76.5%) of RT078 genomes were tetM positive. Multiple additional tetracycline resistance determinants were also identified (including efflux pump tet40), frequently sharing a high level of nucleotide sequence identity (up to 100%) with sequences found in the pig pathogen Streptococcus suis and in other zoonotic pathogens such as Campylobacter jejuni and Campylobacter coli Each RT078 tetM clonal expansion lacked geographic structure, indicating rapid, recent international spread. Resistance determinants for C. difficile infection-triggering antimicrobials, including fluoroquinolones and clindamycin, were comparatively rare in RT078. Tetracyclines are used intensively in agriculture; this selective pressure, plus rapid, international spread via the food chain, may explain the increased RT078 prevalence in humans. Our work indicates that the use of antimicrobials outside the health care environment has selected for resistant organisms, and in the case of RT078, has contributed to the emergence of a human pathogen.IMPORTANCEClostridium difficile PCR ribotype 078 (RT078) has multiple reservoirs; many are agricultural. Since 2005, this genotype has been increasingly associated with human infections in both clinical settings and the community. Investigations of RT078 whole-genome sequences revealed that tetracycline resistance had been acquired on multiple independent occasions. Phylogenetic analysis revealed a rapid, recent increase in numbers of closely related tetracycline-resistant RT078 (clonal expansions), suggesting that tetracycline selection has strongly influenced its recent evolutionary history. We demonstrate recent international spread of emergent, tetracycline-resistant RT078. A similar tetracycline-positive clonal expansion was also identified in unrelated nontoxigenic C. difficile, suggesting that this process may be widespread and may be independent of disease-causing ability. Resistance to typical C. difficile infection-associated antimicrobials (e.g., fluoroquinolones, clindamycin) occurred only sporadically within RT078. Selective pressure from tetracycline appears to be a key factor in the emergence of this human pathogen and the rapid international dissemination that followed, plausibly via the food chain.
KW - Clostridium difficile
KW - PCR ribotype 078
KW - emerging pathogen
KW - phylogenetic analysis
KW - tetracycline resistance
KW - whole-genome sequencing
KW - Phylogenetic analysis
KW - Tetracycline resistance
KW - Whole-genome sequencing
KW - Emerging pathogen
UR - http://www.scopus.com/inward/record.url?scp=85062827436&partnerID=8YFLogxK
U2 - 10.1128/mBio.02790-18
DO - 10.1128/mBio.02790-18
M3 - Article
C2 - 30862754
SN - 2150-7511
VL - 10
SP - 1
EP - 19
JO - MBio
JF - MBio
IS - 2
M1 - e02790-18
ER -