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Comparative immunology, microbiology and infectious diseases2007; 30(3); 163-174; doi: 10.1016/j.cimid.2006.11.006

Toxin production by and adhesive properties of Clostridium difficile isolated from humans and horses with antibiotic-associated diarrhea.

Abstract: Clostridium difficile is a common nosocomial pathogen in humans and animals that causes diarrhea and colitis following antibiotic therapy. Isolates of C. difficile obtained from faecal material from 20 human patients and 6 equine subjects with antibiotic-associated diarrhea were investigated regarding production of toxins A and B, their capacity to adhere to the human intestinal Caco-2 cell line and equine intestinal cells, and for the presence of fimbriae. The results showed that most (17/20) of the human clinical isolates produced both toxins A and B. One of the human isolates proved toxin A-negative/toxin B-positive. All (6/6) horse isolates were positive for both toxins A and B. Both the human and horse isolates possessed the capacity to adhere, to varying degree, to human and equine intestinal cells. It appeared that human isolates produced greater amounts of toxin B, and that there was a host-species dependency on ability to attach to intestinal epithelial cells. No fimbriae were found in any of the investigated isolates.
Publication Date: 2007-01-19 PubMed ID: 17239950DOI: 10.1016/j.cimid.2006.11.006Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research studies the production of toxins and adhesive properties of Clostridium difficile, a bacterium causing diarrhea and colitis in both humans and horses following antibiotic treatment. The study examines bacteria from 20 human patients and 6 horses, focusing on toxins, adherence to intestinal cells, and the presence of fimbriae.

Background on Clostridium difficile

  • In hospitals and animal clinics, Clostridium difficile (C. difficile) is a common bacterium that leads to diarrhea and colitis, inflammation of the colon, after antibiotic therapy. Antibiotics can disturb the balance of bacteria in the gut, allowing C. difficile to grow and release toxins.

Toxin Production of C. difficile

  • The bacteria produce toxins A and B, both of which are responsible for the conditions mentioned. Accordingly, the study assesses these toxins from bacteria in humans and horses treated with antibiotics.
  • Results revealed that a large portion (17 out of 20) of the human bacterial isolates released both toxins. Meanwhile, one isolate produced only toxin B, and all 6 horse isolates produced both toxins.
  • The research observed more production of toxin B in human isolates, implying a potential difference in the bacteria’s impact between species.

Adhesive Properties of C. difficile

  • Part of the study looked into the bacterium’s ability to adhere to the lining of the intestinal cells—specifically the human cell line called Caco-2 and horse intestinal cells.
  • The data indicated that both human and equine bacterial isolates have varying degrees of adherence ability to the cells of their respective species. This signifies that there might be a host-species influence on the attachment ability of the bacterium to intestinal cells.

Presence of Fimbriae

  • The research also investigated the presence of fimbriae, thin appendages on the surface of some bacteria that enable them to stick to surfaces or cells.
  • However, the study did not find fimbriae in any of the analyzed isolates, both human and equine. This is a significant finding, as fimbriae are often linked to the ability of bacteria to cause disease.

Overall, the research offers important insights into the behavior of C. difficile, particularly its toxin production and adherence property. The lack of fimbriae in the bacteria offers new avenues for understanding the mechanisms this bacterium uses to cause disease.

Cite This Article

APA
Taha S, Johansson O, Rivera Jonsson S, Heimer D, Krovacek K. (2007). Toxin production by and adhesive properties of Clostridium difficile isolated from humans and horses with antibiotic-associated diarrhea. Comp Immunol Microbiol Infect Dis, 30(3), 163-174. https://doi.org/10.1016/j.cimid.2006.11.006

Publication

ISSN: 0147-9571
NlmUniqueID: 7808924
Country: England
Language: English
Volume: 30
Issue: 3
Pages: 163-174

Researcher Affiliations

Taha, Sawsan
  • Department of Biomedical Sciences and Veterinary Public Health, Faculty of Veterinary Medicine and Animal Science, SLU, Box 7036, 750 07 Uppsala, Sweden.
Johansson, Orjan
    Rivera Jonsson, Stephan
      Heimer, Daniel
        Krovacek, Karel

          MeSH Terms

          • Animals
          • Bacterial Adhesion
          • Bacterial Toxins / metabolism
          • Caco-2 Cells
          • Clostridioides difficile / cytology
          • Clostridioides difficile / metabolism
          • Clostridioides difficile / pathogenicity
          • Clostridium Infections / microbiology
          • Clostridium Infections / pathology
          • Clostridium Infections / veterinary
          • Diarrhea / microbiology
          • Diarrhea / pathology
          • Diarrhea / veterinary
          • Enterocolitis, Pseudomembranous / microbiology
          • Enterocolitis, Pseudomembranous / pathology
          • Enterocolitis, Pseudomembranous / veterinary
          • Enterotoxins / metabolism
          • Feces / microbiology
          • Fimbriae, Bacterial / metabolism
          • Horse Diseases / microbiology
          • Horse Diseases / pathology
          • Horses
          • Humans
          • Intestines / cytology

          Citations

          This article has been cited 3 times.
          1. Awad MM, Johanesen PA, Carter GP, Rose E, Lyras D. Clostridium difficile virulence factors: Insights into an anaerobic spore-forming pathogen. Gut Microbes 2014;5(5):579-93.
            doi: 10.4161/19490976.2014.969632pubmed: 25483328google scholar: lookup
          2. Wetterwik KJ, Trowald-Wigh G, Fernström LL, Krovacek K. Clostridium difficile in faeces from healthy dogs and dogs with diarrhea. Acta Vet Scand 2013 Mar 12;55(1):23.
            doi: 10.1186/1751-0147-55-23pubmed: 23497714google scholar: lookup
          3. Roberts CL, Keita AV, Parsons BN, Prorok-Hamon M, Knight P, Winstanley C, O' Kennedy N, Söderholm JD, Rhodes JM, Campbell BJ. Soluble plantain fibre blocks adhesion and M-cell translocation of intestinal pathogens. J Nutr Biochem 2013 Jan;24(1):97-103.
            doi: 10.1016/j.jnutbio.2012.02.013pubmed: 22818716google scholar: lookup