4.8 Article

High-fat diet-induced colonocyte dysfunction escalates microbiota-derived trimethylamine N-oxide

Journal

SCIENCE
Volume 373, Issue 6556, Pages 813-+

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aba3683

Keywords

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Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) by the Ministry of Education [2020R1A6A3A03037326]
  2. Vaadia-BARD Postdoctoral Fellowship [FI-5052014]
  3. Public Health Service Grant [AI044170, AI096528, AI112445, AI112949, AI146432, AI153069, TR001861]
  4. Dorothy Beryl and Theodore Roe Austin Pathology Research Fund [T32AI112541, T32DK007673-07, T32ES007028-46]
  5. U.S. Department of Agriculture (USDA) [2032-51530-025-00D]
  6. USDA/NIFA [2015-67015-22930]
  7. Crohn's and Colitis Foundation of America Senior Investigator Award [650976]
  8. V Foundation for Cancer Research [V2020-013]
  9. Vanderbilt Digestive Disease Pilot and Feasibility grant [P30 058404]
  10. ACS Institutional Research Grant [IRG-19-139-59]
  11. VICC GI SPORE grant [P50CA236733]
  12. United States-Israel Binational Science Foundation [2019136]
  13. Vanderbilt Institute for Clinical and Translational Research Grant [VR53102, VR54267]
  14. National Research Foundation of Korea [2020R1A6A3A03037326] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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It was found that chronic exposure to a high-fat diet can increase levels of circulating trimethlamine N-oxide, a potentially harmful metabolite generated by gut microbiota.
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.

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