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High-fat diet–induced colonocyte dysfunction escalates microbiota-derived trimethylamine N-oxide.
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- Author(s): Yoo, Woongjae; Zieba, Jacob K.; Foegeding, Nora J.; Torres, Teresa P.; Shelton, Catherine D.; Shealy, Nicolas G.; Byndloss, Austin J.; Cevallos, Stephanie A.; Gertz, Erik; Tiffany, Connor R.; Thomas, Julia D.; Litvak, Yael; Nguyen, Henry; Olsan, Erin E.; Bennett, Brian J.; Rathmell, Jeffrey C.; Major, Amy S.; Bäumler, Andreas J.; Byndloss, Mariana X.
- Source:
Science. 8/13/2021, Vol. 373 Issue 6556, p813-818. 6p. 1 Color Photograph, 1 Diagram, 2 Graphs.
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- Abstract:
A Western-style, high-fat diet promotes cardiovascular disease, in part because it is rich in choline, which is converted to trimethylamine (TMA) by the gut microbiota. However, whether diet-induced changes in intestinal physiology can alter the metabolic capacity of the microbiota remains unknown. Using a mouse model of diet-induced obesity, we show that chronic exposure to a high-fat diet escalates Escherichia coli choline catabolism by altering intestinal epithelial physiology. A high-fat diet impaired the bioenergetics of mitochondria in the colonic epithelium to increase the luminal bioavailability of oxygen and nitrate, thereby intensifying respiration-dependent choline catabolism of E. coli. In turn, E. coli choline catabolism increased levels of circulating trimethlamine N-oxide, which is a potentially harmful metabolite generated by gut microbiota. [ABSTRACT FROM AUTHOR]
- Abstract:
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