Abstract
Crohn’s disease (CD) is a chronic inflammatory bowel disease (IBD). Mycobacterium avium, which causes Johne’s disease in ruminants, has been suggested as a potential CD trigger due to shared pathology, but early epithelial responses remain unclear. This study established a mouse small intestinal organoid (mSIO) model of M. avium infection to assess CD-related inflammation. Infected mSIOs were examined by confocal microscopy, block-face scanning electron microscopy, and macrophage co-culture to track bacterial localization and immune cell behavior. The data give unprecedent dynamic and super high resolution insights in the responses of gut cells to mycobacterial infection. RNA-seq with GSEA revealed strong induction of inflammatory genes and enrichment of pro-inflammatory pathways. Comparative analysis with CD-humanized mouse data showed overlapping gene expression and enrichment of the IBD signaling pathway. Notably, Mmp7, which can be linked to epithelial remodeling and inflammation, was a common marker in both models. This study presents a robust mSIO model of M. avium infection that recapitulates features of CD-associated inflammation both with high-resolution imaging and transcriptomics and identifies Mmp7 as a potential molecular link between infection and CD-like pathology.
| Original language | English |
|---|---|
| Article number | 2630483 |
| Journal | Gut Microbes |
| Volume | 18 |
| Issue number | 1 |
| Early online date | 13 Feb 2026 |
| DOIs | |
| Publication status | Published - 2026 |
Keywords
- Crohn’s disease
- MMP7
- Mycobacterium avium
- serial block-face scanning electron microscopy
- small intestinal organoids
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