Prosurvival Pathway Protects From Clostridioides difficile Toxin-Mediated Cell Death

J Infect Dis. 2024 May 15;229(5):1519-1522. doi: 10.1093/infdis/jiad481.

Abstract

There is an urgent need for new nonantibiotic-based treatment strategies for Clostridioides difficile infection. C. difficile toxin B (TcdB) is a virulent factor that is essential for causing disease. Here, we investigated whether a survival-signaling pathway could protect against TcdB. We found significant increase in caspase-3 apoptotic activity in intestinal epithelial cells of mice exposed to TcdB. Subsequently, activation of the MIF-CD74-Akt prosurvival signaling pathway blocked TcdB-induced caspase-3 activity and intestinal epithelial cell death. This brief report provides proof-of-concept that targeting prosurvival pathways may represent a unique antibiotic-independent strategy for protecting against C. difficile toxin-mediated cell death.

Keywords: C difficile; Akt; apoptosis; caspase; cell death; cell survival; toxin.

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Bacterial Proteins* / metabolism
  • Bacterial Toxins* / metabolism
  • Bacterial Toxins* / toxicity
  • Caspase 3 / metabolism
  • Cell Death / drug effects
  • Clostridioides difficile*
  • Clostridium Infections / microbiology
  • Clostridium Infections / prevention & control
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Epithelial Cells / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction* / drug effects

Substances

  • Bacterial Toxins
  • Bacterial Proteins
  • Caspase 3
  • Proto-Oncogene Proteins c-akt