Clostridioides difficile stimulates CCL20 expression in human colonoid monolayers in a transwell-based co-culture system that supports its anaerobic growth

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Authors: Paola Zucchi, Adrianne D. Gladden, Andrew W. Day, Jules Dressler, Revathi Govind, Mohammad Almeqdadi, Jatin Roper, A.T. Tai, Rebecca Batorsky, Carol A. Kumamoto
Cited by: 1
References: 56

Abstract

ABSTRACT The pathogenic bacterium Clostridioides difficile is a major cause of antibiotic-associated diarrheal disease. Treatment of the disease is challenging because antibiotics used for treatment may also perpetuate the conditions that contributed to initial susceptibility. Elucidating the mechanisms of C. difficile /intestinal epithelium interaction is needed to facilitate the development of new therapeutic options. The studies described in this communication demonstrate the development of a tissue culture system that supported the growth of C. difficile in co-culture with a model of the human intestinal epithelium produced from colonoids, organoids derived from human colonic biopsies. Epithelial cell responses to C. difficile included upregulation of CCL20 , encoding a chemokine that was previously shown to be upregulated in response to C. difficile challenge. Additionally, bacteria associated with the monolayer in a non-toxin dependent manner. This system will support future investigation of epithelium/ C. difficile interactions during CDI and identification of mechanisms that drive pathogenesis by C. difficile in the human intestine.

Fields of Study & Subjects

Clostridium difficile and Clostridium perfringens research Gastrointestinal motility and disorders Helicobacter pylori-related gastroenterology studies

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
29 April 2026
Language
EN
Document type
Preprint