Cellular Uptake and Mode-of-Action of Clostridium difficile Toxins

Adv Exp Med Biol. 2018:1050:77-96. doi: 10.1007/978-3-319-72799-8_6.

Abstract

Research on the human gut pathogen Clostridium difficile and its toxins has gained much attention, particularly as a consequence of the increasing threat to human health presented by emerging hypervirulent strains. Toxin A (TcdA) and B (TcdB) are the two major virulence determinants of C. difficile. Both are single-chain proteins with a similar multidomain architecture. Certain hypervirulent C. difficile strains also produce a third toxin, namely binary toxin CDT (Clostridium difficile transferase). As C. difficile toxins are the causative agents of C. difficile-associated diseases (CDAD), such as antibiotics-associated diarrhea and pseudomembranous colitis, considerable efforts have been expended to unravel their molecular mode-of-action and the cellular mechanisms responsible for their uptake. Notably, a high proportion of studies on C. difficile toxins were performed in European laboratories. In this chapter we will highlight important recent advances in C. difficile toxins research.

Keywords: Bacterial disease; Bacterial toxins; Clostridium difficile; Toxin receptor; Toxin uptake.

Publication types

  • Review

MeSH terms

  • Animals
  • Bacterial Toxins / chemistry
  • Bacterial Toxins / metabolism*
  • Bacterial Toxins / toxicity*
  • Clostridioides difficile
  • Clostridium Infections / microbiology
  • Endocytosis / drug effects
  • Humans

Substances

  • Bacterial Toxins