Cellular and Molecular Gastroenterology and HepatologyMicrobiologyPeer-reviewed journal article
Dietary protein source mediates colitis pathogenesis through bacterial modulation of bile acids
Simon M. GrayiD, Michael C. Wood, Samantha C. MulkeeniD, Sunjida Ahmed, Shrey D ThakeriD, Bo Chen, William R. SanderiD, Vladimira BibevaiD, Xiaoyue Zhang, Jie YangiD, Jeremy HerzogiD, Anh D. Moss, Shiying ZhangiD, Belgin DoganiD, Kenneth W. Simpson, Ryan Balfour SartoriD, David C. MontroseiD
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Abstract
Introductory paragraphEvidence-based dietary recommendations for individuals with inflammatory bowel diseases (IBD) are limited. Red meat consumption is associated with increased IBD incidence and relapse in patients, suggesting that switching to a plant-based diet may limit gut inflammation. However, the mechanisms underlying the differential effects of these diets remain poorly understood. Feeding diets containing plant- or animal-derived proteins to murine colitis models revealed that mice given a beef protein (BP) diet exhibited the most severe colitis, while mice fed pea protein (PP) developed mild inflammation. The colitis-promoting effects of BP were microbially-mediated as determined by bacterial elimination or depletion and microbiota transplant studies. In the absence of colitis, BP-feeding reduced abundance of Lactobacillus johnsonii and Turicibacter sanguinis and expanded Akkermansia muciniphila, which localized to the mucus in association with decreased mucus thickness and quality. BP-fed mice had elevated primary and conjugated fecal bile acids (BAs), and taurocholic acid administration to PP-fed mice worsened colitis. Dietary psyllium protected against BP-mediated inflammation, restored BA-modulating commensals and normalized BA ratios. Collectively, these data suggest that the protein component of red meat may be responsible, in part, for the colitis-promoting effects of this food source and provide insight into dietary factors that may influence IBD severity.
- organism: mouse
- assay: bulk RNA-seq
- research focus: host-pathogen & immune response
- approach: experimental assay
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