| Literature DB >> 32668218 |
Jee-Yon Lee1, Stephanie A Cevallos2, Mariana X Byndloss2, Connor R Tiffany2, Erin E Olsan2, Brian P Butler3, Briana M Young2, Andrew W L Rogers2, Henry Nguyen2, Kyongchol Kim4, Sang-Woon Choi4, Eunsoo Bae4, Je Hee Lee5, Ui-Gi Min5, Duk-Chul Lee6, Andreas J Bäumler7.
Abstract
The clinical spectra of irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD) intersect to form a scantily defined overlap syndrome, termed pre-IBD. We show that increased Enterobacteriaceae and reduced Clostridia abundance distinguish the fecal microbiota of pre-IBD patients from IBS patients. A history of antibiotics in individuals consuming a high-fat diet was associated with the greatest risk for pre-IBD. Exposing mice to these risk factors resulted in conditions resembling pre-IBD and impaired mitochondrial bioenergetics in the colonic epithelium, which triggered dysbiosis. Restoring mitochondrial bioenergetics in the colonic epithelium with 5-amino salicylic acid, a PPAR-γ (peroxisome proliferator-activated receptor gamma) agonist that stimulates mitochondrial activity, ameliorated pre-IBD symptoms. As with patients, mice with pre-IBD exhibited notable expansions of Enterobacteriaceae that exacerbated low-grade mucosal inflammation, suggesting that remediating dysbiosis can alleviate inflammation. Thus, environmental risk factors cooperate to impair epithelial mitochondrial bioenergetics, thereby triggering microbiota disruptions that exacerbate inflammation and distinguish pre-IBD from IBS.Entities:
Keywords: antibiotics; dysbiosis; high-fat diet; inflammatory bowel disease; irritable bowel syndrome; microbiota
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Year: 2020 PMID: 32668218 PMCID: PMC7429289 DOI: 10.1016/j.chom.2020.06.001
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023