Post-infectious ibs following Clostridioides difficile infection; role of microbiota and implications for treatment

Dana Taghaddos1, Zarwa Saqib1, Xiaopeng Bai2

  • 1Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Insights

Up to 25% of patients recovering from antibiotic-treated Clostridioides difficile infection (CDI) develop symptoms similar to Post-Infectious Irritable Bowel Syndrome (PI-IBS). Microbiota-directed therapies, like fecal microbial transplant, may prevent PI-IBS by restoring gut health after primary CDI.

Area of Science:

  • Gastroenterology
  • Microbiology
  • Immunology

Background:

  • Clostridioides difficile infection (CDI) can lead to persistent functional gut symptoms resembling Post-Infectious Irritable Bowel Syndrome (PI-IBS) in up to 25% of patients.
  • Current management for persistent symptoms after CDI involves a dilemma between further antibiotic use or conservative symptom management.

Purpose of the Study:

  • To review the literature on CDI-related PI-IBS and compare it with general PI-IBS.
  • To explore proposed mechanisms underlying CDI-related PI-IBS, including the roles of C. difficile toxins and gut microbiota dysbiosis.
  • To discuss therapeutic implications, particularly microbiota-directed therapies for primary CDI.

Main Methods:

  • Literature review of studies on CDI-related PI-IBS and PI-IBS.
  • Analysis of proposed pathogenic mechanisms involving C. difficile toxins and gut microbiota.
  • Discussion of current and potential therapeutic strategies.

Main Results:

  • Gut dysfunction post-CDI may be initiated by toxin-induced damage to enteroglial cells.
  • A dysbiotic gut microbiota is implicated in maintaining the chronic PI-IBS phenotype after CDI.
  • Fecal Microbial Transplant (FMT) is currently used for recurrent CDI (rCDI) but its potential in primary CDI is explored.

Conclusions:

  • Microbiota-directed therapies, including novel microbial transfer strategies, warrant consideration for primary CDI to prevent or mitigate PI-IBS.
  • Preventing further antibiotic disruption of the microbiota may be key to avoiding long-term functional symptoms.
  • Clinical trials are recommended to evaluate microbial transfer therapy for primary CDI to prevent both rCDI and CDI-related PI-IBS.

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