Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • What's Your Diagnosis
  • Published:

Diagnosis | Clostridium difficile–induced typhlitis and colitis

This is a preview of subscription content, access via your institution

Access options

Figure 2: Section of cecum from a hamster that died suddenly (Fig. 1) stained with hematoxylin and eosin.
Figure 3: PCR gel analysis of cecal tissue from a hamster that died suddenly using two primers specific for C. difficile toxins A (a) and B (b).

References

  1. Ryan, K.J. Pathogenic bacteria. in Sherris Medical Microbiology 4th edn. (eds. Ryan, K.J. & Ray, C.G.) 322–324 (McGraw-Hill, Columbus, OH, 2004).

    Google Scholar 

  2. Taylor, N.S., Thorne, G.M. & Bartlett, J.G. Comparison of two toxins produced by Clostridium difficile. Infect. Immun. 34, 1036–1043 (1981).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Lyerly, D.M., Saum, K.E., MacDonald, D.K. & Wilkins, T.D. Effects of Clostridium difficile toxins given intragastrically to animals. Infect. Immun. 47, 349–352 (1985).

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Kamaras, J. & Murrell, W.G. Intestinal epithelial damage in SIDS babies and its similarity to that caused by bacterial toxins in the rabbit. Pathology 33, 197–203 (2001).

    Article  CAS  Google Scholar 

  5. Lima, A.A., Lyerly, D.M., Wilkins, T.D., Innes, D.J. & Guerrant, R.L. Effects of Clostridium difficile toxins A and B in rabbit small and large intestine in vivo and on cultured cells in vitro. Infect. Immun. 56, 582–588 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  6. van den Berg, R.J. et al. Characterization of toxin A-negative, toxin B-positive Clostridium difficile isolates from outbreaks in different countries by amplified fragment length polymorphism and PCR ribotyping. J. Clin. Microbiol. 42, 1035–1041 (2004).

    Article  CAS  Google Scholar 

  7. Ryden, E.B., Lipman, N.S., Taylor, N.S., Rose, R. & Fox, J.G. Clostridium difficile typhlitis associated with cecal mucosal hyperplasia in Syrian hamsters. Lab. Anim. Sci. 41, 553–558 (1991).

    CAS  PubMed  Google Scholar 

  8. Larson, H.E., Price, A.B., Honour, P. & Borriello, S.P. Clostridium difficile and the aetiology of pseudomembranous colitis. Lancet 1, 1063–1066 (1978).

    Article  CAS  Google Scholar 

  9. Small, J.D. Fatal enterocolitis in hamsters given lincomycin hydrochloride. Lab. Anim. Care 18, 411–420 (1968).

    CAS  PubMed  Google Scholar 

  10. Lowe, B.R., Fox, J.G. & Bartlett JG. Clostridium difficile–associated cecitis in guinea pigs exposed to penicillin. Am. J. Vet. Res. 41, 1277–1279 (1980).

    CAS  PubMed  Google Scholar 

  11. Naaber, P. & Mikelsaar, M. Antibiotic-compromised murine model of Clostridium difficile infection. Microecol. Ther. 25, 201–205 (1995).

    Google Scholar 

  12. Czuprynski, C.J., Johnson, W.J., Balish, E. & Wilkins, T. Pseudomembranous colitis in Clostridium difficile-monoassociated rats. Infect. Immun. 39, 1368–1376 (1983).

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Carman, R.J. & Evans, R.H. Experimental and spontaneous clostridial enteropathies of laboratory and free living lagomorphs. Lab. Anim. Sci. 34, 443–452 (1984).

    CAS  PubMed  Google Scholar 

  14. Rolland, R.M., Chalifoux, L.V., Snook, S.S., Ausman, L.M. & Johnson, L.D. Five spontaneous deaths associated with Clostridium difficile in a colony of cotton-top tamarins (Saguinus oedipus). Lab. Anim. Sci. 47, 472–476 (1997).

    CAS  PubMed  Google Scholar 

  15. Peeters, J.E., Geeroms, R., Carman, R.J. & Wilkins, T.D. Significance of Clostridium spiroforme in the enteritis-complex of commercial rabbits. Vet. Microbiol. 12, 25–31 (1986).

    Article  CAS  Google Scholar 

  16. Perkins, S.E., Fox, J.G., Taylor, N.S., Green, D.L. & Lipman, N.S. Detection of Clostridium difficile toxins from the small intestine and cecum of rabbits with naturally acquired enterotoxemia. Lab. Anim. Sci. 45, 379–384 (1995).

    CAS  PubMed  Google Scholar 

  17. Bartlett, J.G., Chang, T.W., Moon, N. & Onderdonk, A.B. Antibiotic-induced lethal enterocolitis in hamsters: studies with eleven agents and evidence to support the pathogenic role of toxin-producing Clostridia. Am. J. Vet. Res. 39, 1525–1530 (1978).

    CAS  PubMed  Google Scholar 

  18. Lusk, R.H. et al. Clindamycin-induced enterocolitis in hamsters. J. Infect. Dis. 137, 464–475 (1978).

    Article  CAS  Google Scholar 

  19. Rehg, J.E. & Lu, Y.S. Clostridium difficile typhlitis in hamsters not associated with antibiotic therapy. J. Am. Vet. Med. Assoc. 181, 1422–1423 (1982).

    CAS  PubMed  Google Scholar 

  20. Blankenship-Paris, T.L., Walton, B.J., Hayes, Y.O. & Chang, J. Clostridium difficile infection in hamsters fed an atherogenic diet. Vet. Pathol. 32, 269–273 (1995).

    Article  CAS  Google Scholar 

  21. Sambol, S.P., Tang, J.K., Merrigan, M.M., Johnson, S. & Gerding, D.N. Infection of hamsters with epidemiologically important strains of Clostridium difficile. J. Infect. Dis. 183, 1760–1766 (2001).

    Article  CAS  Google Scholar 

  22. Nambiar, P.R. et al. Progressive proliferative and dysplastic typhlocolitis in aging Syrian hamsters naturally infected with Helicobacter spp.: a spontaneous model of inflammatory bowel disease. Vet. Pathol. 43, 2–14 (2006).

    Article  CAS  Google Scholar 

  23. Bolton, R.P., Tait, S.K., Dear, P.R. & Losowsky, M.S. Asymptomatic neonatal colonisation by Clostridium difficile. Arch. Dis. Child. 59, 466–472 (1984).

    Article  CAS  Google Scholar 

  24. Borriello, S.P. & Wilcox, M.H. Clostridium difficile infections of the gut: the unanswered questions. J. Antimicrob. Chemother. 41 (Suppl. C), 67–69 (1998).

    Article  CAS  Google Scholar 

  25. Johnson, S. et al. Nosocomial Clostridium difficile colonisation and disease. Lancet. 336, 97–100 (1990).

    Article  CAS  Google Scholar 

  26. McFarland, L.V., Mulligan, M.E., Kwok, R.Y. & Stamm, W.E. Nosocomial acquisition of Clostridium difficile infection. N. Engl. J. Med. 320, 204–210 (1989).

    Article  CAS  Google Scholar 

  27. Bignardi, G.E. Risk factors for Clostridium difficile infection. J. Hosp. Infect. 40, 1–15 (1998).

    Article  CAS  Google Scholar 

  28. Clabots, C.R., Johnson, S., Olson, M.M., Peterson, L.R. & Gerding, D.N. Acquisition of Clostridium difficile by hospitalized patients: evidence for colonized new admissions as a source of infection. J. Infect. Dis. 166, 561–567 (1992).

    Article  CAS  Google Scholar 

  29. Viscidi, R., Willey, S. & Bartlett, J.G. Isolation rates and toxigenic potential of Clostridium difficile isolates from various patient populations. Gastroenterology 81, 5–9 (1981).

    Article  CAS  Google Scholar 

  30. Borriello, S.P., Honour, P., Turner, T. & Barclay, F. Household pets as a potential reservoir for Clostridium difficile infection. J. Clin. Pathol. 36, 84–87 (1983).

    Article  CAS  Google Scholar 

  31. Madewell, B.R. et al. Clostridium difficile: a survey of fecal carriage in cats in a veterinary medical teaching hospital. J. Vet. Diagn. Invest. 11, 50–54 (1999).

    Article  CAS  Google Scholar 

  32. Riley, T.V., Adams, J.E., O'Neill, G.L. & Bowman, R.A. Gastrointestinal carriage of Clostridium difficile in cats and dogs attending veterinary clinics. Epidemiol. Infect. 107, 659–665 (1991).

    Article  CAS  Google Scholar 

  33. Struble, A.L. et al. Fecal shedding of Clostridium difficile in dogs: a period prevalence survey in a veterinary medical teaching hospital. J. Vet. Diagn. Invest. 6, 342–347 (1994).

    Article  CAS  Google Scholar 

  34. Ratnaike, R.N. & Jones, T.E. Mechanisms of drug-induced diarrhoea in the elderly. Drugs Aging 13, 245–253 (1998).

    Article  CAS  Google Scholar 

  35. Wilson, K.H. & Perini, F. Role of competition for nutrients in suppression of Clostridium difficile by the colonic microflora. Infect. Immun. 56, 2610–2614 (1988).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Baverud, V., Gustafsson, A., Franklin, A., Lindholm, A. & Gunnarsson, A. Clostridium difficile associated with acute colitis in mature horses treated with antibiotics. Equine Vet. J. 29, 279–284 (1997).

    Article  CAS  Google Scholar 

  37. Johnson, S. et al. Prospective, controlled study of vinyl glove use to interrupt Clostridium difficile nosocomial transmission. Am. J. Med. 88, 37–140 (1990).

    Article  Google Scholar 

  38. Madewell, B.R. et al. Apparent outbreaks of Clostridium difficile–associated diarrhea in horses in a veterinary medical teaching hospital. J. Vet. Diagn. Invest. 7, 343–346 (1995).

    Article  CAS  Google Scholar 

  39. Delmee, M. Laboratory diagnosis of Clostridium difficile disease. Clin. Microbiol. Infect. 7, 411–416 (2001).

    Article  CAS  Google Scholar 

  40. Weese, J.S., Staempfli, H.R. & Prescott, J.F. Survival of Clostridium difficile and its toxins in equine feces: implications for diagnostic test selection and interpretation. J. Vet. Diagn. Invest. 12, 332–336 (2000).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank Howard Wilson (University of Missouri-Columbia) for the histology and PCR figures. Erin O'Connor was supported by a Mission Enhancement grant from the University of Missouri.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Diagnosis | Clostridium difficile–induced typhlitis and colitis. Lab Anim 39, 100–102 (2010). https://doi.org/10.1038/laban0410-100

Download citation

  • Issue date:

  • DOI: https://doi.org/10.1038/laban0410-100

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing