Clostridium difficile toxin B induces apoptosis in intestinal cultured cells

Infect Immun. 1998 Jun;66(6):2660-5. doi: 10.1128/IAI.66.6.2660-2665.1998.

Abstract

Toxigenic strains of the anaerobic bacterium Clostridium difficile produce at least two large, single-chain protein exotoxins involved in the pathogenesis of antibiotic-associated diarrhea and colitis. Toxin A (CdA) is a cytotoxic enterotoxin, while toxin B (CdB) is a more potent cytotoxin lacking enterotoxic activity. This study dealt with CdB, providing the first evidence that intestinal cells exposed to this toxin exhibit typical features of apoptosis in that a significant proportion of the treated cells displayed nuclear fragmentation and chromatin condensation. In keeping with ultrastructural data, CdB-treated cells showed the typical flow cytometric hallmark of apoptosis consisting of a distinct sub-G1 peak. The CdB-induced apoptotic response was dose and time dependent and not simply due to the actin-disrupting effect of the toxin or to the subsequent impairment of cell anchorage. Rather, the inhibition of proteins belonging to the Rho family due to CdB seems to play a role in the induction of apoptosis in intestinal cells. The origin of cells and the growth rate may also be cofactors relevant to such a response.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / drug effects
  • Animals
  • Apoptosis*
  • Bacterial Proteins*
  • Bacterial Toxins / pharmacology*
  • Cell Size / drug effects
  • Cells, Cultured
  • Clostridioides difficile*
  • Dose-Response Relationship, Drug
  • GTP Phosphohydrolases / metabolism
  • GTP-Binding Proteins / metabolism
  • Humans
  • Intestines / cytology
  • Intestines / drug effects*
  • Protein Biosynthesis
  • Rats
  • rho GTP-Binding Proteins

Substances

  • Actins
  • Bacterial Proteins
  • Bacterial Toxins
  • toxB protein, Clostridium difficile
  • GTP Phosphohydrolases
  • GTP-Binding Proteins
  • rho GTP-Binding Proteins