| Summary: | Anastomotic leakage is a major complication following colorectal surgery leading to peritonitis, complications, and mortality. <i>Akkermansia muciniphila</i> has shown beneficial effects on the gut barrier function. Whether <i>A. muciniphila</i> reduces peritonitis and mortality during colonic leakage is unknown. Whether <i>A. muciniphila</i> can directly modulate the expression of genes in the colonic mucosa in humans has never been studied. We investigated the effects of a pretreatment (14 days) with live <i>A. muciniphila</i> prior to surgical colonic perforation on peritonitis, mortality, and wound healing. We used mice with an inducible intestinal-epithelial-cell-specific deletion of MyD88 (IEC-MyD88 KO) to investigate the role of the innate immune system in this context. In a proof-of-concept pilot study, healthy humans were exposed to <i>A. muciniphila</i> for 2 h and colonic biopsies taken before and after colonic instillation for transcriptomic analysis. Seven days after colonic perforation, <i>A.-muciniphila</i>-treated mice had significantly lower mortality and severity of peritonitis. This effect was associated with significant improvements of wound histological healing scores, higher production of IL22, but no changes in the mucus layer thickness or genes involved in cell renewal, proliferation, or differentiation. All these effects were abolished in IEC-MyD88 KO mice. Finally, human subjects exposed to <i>A. muciniphila</i> exhibited an increased level of the bacterium at the mucus level 2 h after instillation and significant changes in the expression of different genes involved in the regulation of cell cycling, gene transcription, immunity, and inflammation in their colonic mucosa. <i>A. muciniphila</i> improves wound healing during transmural colonic wall defect through mechanisms possibly involving IL22 signaling and requiring MyD88 in the intestinal cells. In healthy humans, colonic administration of <i>A. muciniphila</i> is well tolerated and changes the expression of genes involved in the immune pathways.
|
|---|