Toxicity assessment of Clostridium difficile toxins in rodent models and protection of vaccination

Vaccine. 2016 Mar 4;34(10):1319-23. doi: 10.1016/j.vaccine.2015.11.026. Epub 2015 Nov 21.

Abstract

Clostridium difficile is the leading cause of hospital-acquired diarrhea, also known as C. difficile associated diarrhea. The two major toxins, toxin A and toxin B are produced by most C. difficile bacteria, but some strains, such as BI/NAP1/027 isolates, produce a third toxin called binary toxin. The precise biological role of binary toxin is not clear but it has been shown to be a cytotoxin for Vero cells. We evaluated the toxicity of these toxins in mice and hamsters and found that binary toxin causes death in both animals similar to toxins A and B. Furthermore, immunization of mice with mutant toxoids of all three toxins provided protection upon challenge with native toxins. These results support the concept that binary toxin contributes to the pathogenicity of C. difficile and provide a method for monitoring the toxicity of binary toxin components in vaccines.

Keywords: Binary toxin; Clostridium difficile toxins; LD(50); Mice model; Protection; Vaccine.

MeSH terms

  • ADP Ribose Transferases / toxicity
  • Animals
  • Bacterial Proteins / toxicity
  • Bacterial Toxins / toxicity*
  • Clostridioides difficile / pathogenicity*
  • Cricetinae
  • Enterotoxins / toxicity
  • Female
  • Lethal Dose 50
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Toxoids / toxicity*

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • Enterotoxins
  • Toxoids
  • tcdA protein, Clostridium difficile
  • toxB protein, Clostridium difficile
  • ADP Ribose Transferases
  • actin-specific ADP-ribosyltransferase, Clostridium