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Journal of medical microbiology2005; 54(Pt 2); 163-166; doi: 10.1099/jmm.0.45805-0

PCR ribotyping of Clostridium difficile isolates originating from human and animal sources.

Abstract: Molecular typing of Clostridium difficile isolates from animals and humans may be useful for evaluation of the possibility for interspecies transmission. The objective of this study was to evaluate C. difficile isolates from domestic animals and humans using PCR ribotyping. Isolates were also tested using PCR for the presence of genes encoding toxins A and B. One hundred and thirty-three isolates of C. difficile from dogs (n = 92), horses (n = 21) and humans (n = 20), plus one each from a cat and a calf, were evaluated. Overall, 23 ribotypes were identified. Of these, nine were identified from dogs, 12 from horses, seven from humans and one each from the cat and calf. In dogs, humans and horses, one or two different ribotypes predominated. Overall, 25 % of isolates from humans were indistinguishable from isolates from one or more animal species. Genes encoding C. difficile toxins A and B were detected in all human, equine and bovine isolates, and in 69 % of canine isolates. While different ribotypes appear to predominate in different mammalian species, several indistinguishable strains may be found in multiple species. This suggests that there is a potential for interspecies transmission of C. difficile and epidemiological studies are warranted.
Publication Date: 2005-01-28 PubMed ID: 15673511DOI: 10.1099/jmm.0.45805-0Google Scholar: Lookup
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  • Journal Article

Summary

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The research was conducted with the aim to investigate potential interspecies transmission of Clostridium difficile, specifically among domestic animals and humans, using PCR ribotyping. The study identified similarities across species, suggesting potential pathways for infection.

Study Overview

  • The research was focused on evaluating the isolation of Clostridium difficile, a bacteria causing infections and conditions like diarrhea and colitis, in humans and animals using PCR ribotyping, a method of identifying the bacteria’s genetic variations. The study further aimed to establish the possibility of interspecies transmission.
  • The researchers evaluated 133 isolates of C. difficile collected from different species including dogs, horses, humans, a cat and a calf.

Findings

  • Each species had varying numbers of identifiable ribotypes. Dogs had nine, horses had twelve, humans had seven, with the cat and calf each having one.
  • It was observed that one or two ribotypes were present in larger numbers across dogs, horses, and humans.
  • The significant finding was that 25% of the human isolates showed no difference from those found in one or more animal species, which gives weight to the perspective of potential interspecies transmission of C. difficile.
  • All human, equine, and bovine isolates, along with 69% of canine isolates, were discovered to have genes encoding C. difficile’s toxins A and B. These toxins are responsible for the harmful effects of the bacteria.

Conclusion

  • While it is noted that different ribotypes seemed to majorly exist in different species, strain similarities across multiple species cannot be dismissed.
  • The study concludes that the presence of similar strains in multiple species indicates a possible pathway for interspecies transmission of C. difficile.
  • Since such transmission can lead to infections in different species, further epidemiological studies are recommended to explore this possibility.

Cite This Article

APA
Arroyo LG, Kruth SA, Willey BM, Staempfli HR, Low DE, Weese JS. (2005). PCR ribotyping of Clostridium difficile isolates originating from human and animal sources. J Med Microbiol, 54(Pt 2), 163-166. https://doi.org/10.1099/jmm.0.45805-0

Publication

ISSN: 0022-2615
NlmUniqueID: 0224131
Country: England
Language: English
Volume: 54
Issue: Pt 2
Pages: 163-166

Researcher Affiliations

Arroyo, Luis G
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada N1G 2W1 2Department of Microbiology, Mount Sinai Hospital, Toronto, Ontario, Canada.
Kruth, Stephen A
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada N1G 2W1 2Department of Microbiology, Mount Sinai Hospital, Toronto, Ontario, Canada.
Willey, Barbara M
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada N1G 2W1 2Department of Microbiology, Mount Sinai Hospital, Toronto, Ontario, Canada.
Staempfli, Henry R
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada N1G 2W1 2Department of Microbiology, Mount Sinai Hospital, Toronto, Ontario, Canada.
Low, Don E
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada N1G 2W1 2Department of Microbiology, Mount Sinai Hospital, Toronto, Ontario, Canada.
Weese, J Scott
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada N1G 2W1 2Department of Microbiology, Mount Sinai Hospital, Toronto, Ontario, Canada.

MeSH Terms

  • Animals
  • Bacterial Proteins / genetics
  • Bacterial Toxins / genetics
  • Cats
  • Cattle
  • Clostridioides difficile / classification
  • Clostridioides difficile / genetics
  • Clostridioides difficile / isolation & purification
  • Clostridium Infections / diagnosis
  • Clostridium Infections / microbiology
  • Clostridium Infections / transmission
  • DNA, Bacterial / analysis
  • Dogs
  • Enterotoxins / genetics
  • Horses
  • Humans
  • Polymerase Chain Reaction
  • RNA, Ribosomal / analysis
  • RNA, Ribosomal / genetics
  • Ribotyping

Citations

This article has been cited 35 times.
  1. Borges AS, Zakia LS, Yu S, Surette MG, Arroyo LG. Isolation of Clostridioides difficile from a Large Animal Veterinary Teaching Hospital Environment. Animals (Basel) 2025 Sep 15;15(18).
    doi: 10.3390/ani15182703pubmed: 41007948google scholar: lookup
  2. Baghani A, Alimohammadi M, Aliramezani A, Talebi M, Mesdaghinia A, Douraghi M. Isolation and characterization of a multidrug-resistant Clostridioides difficile toxinotype V from municipal wastewater treatment plant. J Environ Health Sci Eng 2020 Dec;18(2):1281-1288.
    doi: 10.1007/s40201-020-00546-0pubmed: 33312642google scholar: lookup
  3. Hernandez BG, Vinithakumari AA, Sponseller B, Tangudu C, Mooyottu S. Prevalence, Colonization, Epidemiology, and Public Health Significance of Clostridioides difficile in Companion Animals. Front Vet Sci 2020;7:512551.
    doi: 10.3389/fvets.2020.512551pubmed: 33062657google scholar: lookup
  4. Thanissery R, McLaren MR, Rivera A, Reed AD, Betrapally NS, Burdette T, Winston JA, Jacob M, Callahan BJ, Theriot CM. Clostridioides difficile carriage in animals and the associated changes in the host fecal microbiota. Anaerobe 2020 Dec;66:102279.
  5. Kachrimanidou M, Tzika E, Filioussis G. Clostridioides (Clostridium) Difficile in Food-Producing Animals, Horses and Household Pets: A Comprehensive Review. Microorganisms 2019 Dec 9;7(12).
    doi: 10.3390/microorganisms7120667pubmed: 31835413google scholar: lookup
  6. Alfayyadh M, Collins DA, Tempone S, McCann R, Armstrong PK, Riley TV, Cook A. Recurrence of Clostridium difficile infection in the Western Australian population. Epidemiol Infect 2019 Jan;147:e153.
    doi: 10.1017/S0950268819000499pubmed: 31063109google scholar: lookup
  7. Aliramezani A, Talebi M, Baghani A, Hajabdolbaghi M, Salehi M, Abdollahi A, Afhami S, Marjani M, Golbabaei F, Boroumand MA, Sarrafnejad A, Yaseri M, Ghourchian S, Douraghi M. Pathogenicity locus determinants and toxinotyping of Clostridioides difficile isolates recovered from Iranian patients. New Microbes New Infect 2018 Sep;25:52-57.
    doi: 10.1016/j.nmni.2018.07.003pubmed: 30094031google scholar: lookup
  8. Andrés-Lasheras S, Martín-Burriel I, Mainar-Jaime RC, Morales M, Kuijper E, Blanco JL, Chirino-Trejo M, Bolea R. Preliminary studies on isolates of Clostridium difficile from dogs and exotic pets. BMC Vet Res 2018 Mar 9;14(1):77.
    doi: 10.1186/s12917-018-1402-7pubmed: 29523201google scholar: lookup
  9. Rabold D, Espelage W, Abu Sin M, Eckmanns T, Schneeberg A, Neubauer H, Möbius N, Hille K, Wieler LH, Seyboldt C, Lübke-Becker A. The zoonotic potential of Clostridium difficile from small companion animals and their owners. PLoS One 2018;13(2):e0193411.
    doi: 10.1371/journal.pone.0193411pubmed: 29474439google scholar: lookup
  10. Ngernsombat C, Sreesai S, Harnvoravongchai P, Chankhamhaengdecha S, Janvilisri T. CD2068 potentially mediates multidrug efflux in Clostridium difficile. Sci Rep 2017 Aug 30;7(1):9982.
    doi: 10.1038/s41598-017-10155-xpubmed: 28855575google scholar: lookup
  11. Nicholson MR, Crews JD, Starke JR, Jiang ZD, DuPont H, Edwards K. Recurrent Clostridium difficile Infection in Children: Patient Risk Factors and Markers of Intestinal Inflammation. Pediatr Infect Dis J 2017 Apr;36(4):379-383.
    doi: 10.1097/INF.0000000000001450pubmed: 27977555google scholar: lookup
  12. Stone NE, Sidak-Loftis LC, Sahl JW, Vazquez AJ, Wiggins KB, Gillece JD, Hicks ND, Schupp JM, Busch JD, Keim P, Wagner DM. More than 50% of Clostridium difficile Isolates from Pet Dogs in Flagstaff, USA, Carry Toxigenic Genotypes. PLoS One 2016;11(10):e0164504.
    doi: 10.1371/journal.pone.0164504pubmed: 27723795google scholar: lookup
  13. Bloomfield LE, Riley TV. Epidemiology and Risk Factors for Community-Associated Clostridium difficile Infection: A Narrative Review. Infect Dis Ther 2016 Sep;5(3):231-51.
    doi: 10.1007/s40121-016-0117-ypubmed: 27370914google scholar: lookup
  14. Zhu S, Zhang H, Zhang X, Wang C, Fan G, Zhang W, Sun G, Chen H, Zhang L, Li Z. Investigation of toxin gene diversity and antimicrobial resistance of Clostridium difficile strains. Biomed Rep 2014 Sep;2(5):743-748.
    doi: 10.3892/br.2014.311pubmed: 25054021google scholar: lookup
  15. Doosti A, Mokhtari-Farsani A. Study of the frequency of Clostridium difficile tcdA, tcdB, cdtA and cdtB genes in feces of Calves in south west of Iran. Ann Clin Microbiol Antimicrob 2014 Jun 5;13:21.
    doi: 10.1186/1476-0711-13-21pubmed: 24903619google scholar: lookup
  16. Gupta A, Khanna S. Community-acquired Clostridium difficile infection: an increasing public health threat. Infect Drug Resist 2014;7:63-72.
    doi: 10.2147/IDR.S46780pubmed: 24669194google scholar: lookup
  17. Sekulovic O, Garneau JR, Néron A, Fortier LC. Characterization of temperate phages infecting Clostridium difficile isolates of human and animal origins. Appl Environ Microbiol 2014 Apr;80(8):2555-63.
    doi: 10.1128/AEM.00237-14pubmed: 24532062google scholar: lookup
  18. Bandelj P, Trilar T, Blagus R, Ocepek M, Rousseau J, Weese JS, Vengust M. Prevalence and molecular characterization of Clostridium difficile isolated from European Barn Swallows (Hirundo rustica) during migration. BMC Vet Res 2014 Feb 8;10:40.
    doi: 10.1186/1746-6148-10-40pubmed: 24507706google scholar: lookup
  19. Janvilisri T, Scaria J, Teng CH, McDonough SP, Gleed RD, Fubini SL, Zhang S, Akey B, Chang YF. Temporal differential proteomes of Clostridium difficile in the pig ileal-ligated loop model. PLoS One 2012;7(9):e45608.
    doi: 10.1371/journal.pone.0045608pubmed: 23029131google scholar: lookup
  20. Schoster A, Arroyo LG, Staempfli HR, Shewen PE, Weese JS. Presence and molecular characterization of Clostridium difficile and Clostridium perfringens in intestinal compartments of healthy horses. BMC Vet Res 2012 Jun 29;8:94.
    doi: 10.1186/1746-6148-8-94pubmed: 22748233google scholar: lookup
  21. Norman KN, Scott HM, Harvey RB, Norby B, Hume ME, Andrews K. Prevalence and genotypic characteristics of Clostridium difficile in a closed and integrated human and swine population. Appl Environ Microbiol 2011 Aug 15;77(16):5755-60.
    doi: 10.1128/AEM.05007-11pubmed: 21724899google scholar: lookup
  22. Scaria J, Ponnala L, Janvilisri T, Yan W, Mueller LA, Chang YF. Analysis of ultra low genome conservation in Clostridium difficile. PLoS One 2010 Dec 8;5(12):e15147.
    doi: 10.1371/journal.pone.0015147pubmed: 21170335google scholar: lookup
  23. Metcalf D, Reid-Smith RJ, Avery BP, Weese JS. Prevalence of Clostridium difficile in retail pork. Can Vet J 2010 Aug;51(8):873-6.
    pubmed: 21037888
  24. Freeman J, Bauer MP, Baines SD, Corver J, Fawley WN, Goorhuis B, Kuijper EJ, Wilcox MH. The changing epidemiology of Clostridium difficile infections. Clin Microbiol Rev 2010 Jul;23(3):529-49.
    doi: 10.1128/CMR.00082-09pubmed: 20610822google scholar: lookup
  25. Janvilisri T, Scaria J, Chang YF. Transcriptional profiling of Clostridium difficile and Caco-2 cells during infection. J Infect Dis 2010 Jul 15;202(2):282-90.
    doi: 10.1086/653484pubmed: 20521945google scholar: lookup
  26. Clements AC, Magalhães RJ, Tatem AJ, Paterson DL, Riley TV. Clostridium difficile PCR ribotype 027: assessing the risks of further worldwide spread. Lancet Infect Dis 2010 Jun;10(6):395-404.
    doi: 10.1016/S1473-3099(10)70080-3pubmed: 20510280google scholar: lookup
  27. Baker AA, Davis E, Rehberger T, Rosener D. Prevalence and diversity of toxigenic Clostridium perfringens and Clostridium difficile among swine herds in the midwest. Appl Environ Microbiol 2010 May;76(9):2961-7.
    doi: 10.1128/AEM.02459-09pubmed: 20208029google scholar: lookup
  28. Janvilisri T, Scaria J, Thompson AD, Nicholson A, Limbago BM, Arroyo LG, Songer JG, Gröhn YT, Chang YF. Microarray identification of Clostridium difficile core components and divergent regions associated with host origin. J Bacteriol 2009 Jun;191(12):3881-91.
    doi: 10.1128/JB.00222-09pubmed: 19376880google scholar: lookup
  29. Indra A, Lassnig H, Baliko N, Much P, Fiedler A, Huhulescu S, Allerberger F. Clostridium difficile: a new zoonotic agent?. Wien Klin Wochenschr 2009;121(3-4):91-5.
    doi: 10.1007/s00508-008-1127-xpubmed: 19280132google scholar: lookup
  30. Jhung MA, Thompson AD, Killgore GE, Zukowski WE, Songer G, Warny M, Johnson S, Gerding DN, McDonald LC, Limbago BM. Toxinotype V Clostridium difficile in humans and food animals. Emerg Infect Dis 2008 Jul;14(7):1039-45.
    doi: 10.3201/eid1407.071641pubmed: 18598622google scholar: lookup
  31. Rodriguez-Palacios A, Staempfli HR, Duffield T, Weese JS. Clostridium difficile in retail ground meat, Canada. Emerg Infect Dis 2007 Mar;13(3):485-7.
    doi: 10.3201/eid1303.060988pubmed: 17552108google scholar: lookup
  32. Keel K, Brazier JS, Post KW, Weese S, Songer JG. Prevalence of PCR ribotypes among Clostridium difficile isolates from pigs, calves, and other species. J Clin Microbiol 2007 Jun;45(6):1963-4.
    doi: 10.1128/JCM.00224-07pubmed: 17428945google scholar: lookup
  33. Rodriguez-Palacios A, Stämpfli HR, Duffield T, Peregrine AS, Trotz-Williams LA, Arroyo LG, Brazier JS, Weese JS. Clostridium difficile PCR ribotypes in calves, Canada. Emerg Infect Dis 2006 Nov;12(11):1730-6.
    doi: 10.3201/eid1211.051581pubmed: 17283624google scholar: lookup
  34. Lefebvre SL, Arroyo LG, Weese JS. Epidemic Clostridium difficile strain in hospital visitation dog. Emerg Infect Dis 2006 Jun;12(6):1036-7.
    doi: 10.3201/eid1206.060115pubmed: 16752477google scholar: lookup
  35. Arroyo LG, Rousseau JD, Staempfli HR, Weese JS. Suspected Clostridium difficile-associated hemorrhagic diarrhea in a 1-week-old elk calf. Can Vet J 2005 Dec;46(12):1130-1.
    pubmed: 16422066