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

Science. 2021 Aug 13;373(6556):813-818. doi: 10.1126/science.aba3683.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Hypoxia
  • Choline / administration & dosage
  • Choline / metabolism
  • Colon / cytology
  • Colon / physiology*
  • Diet, High-Fat*
  • Energy Metabolism
  • Epithelial Cells / physiology
  • Escherichia coli / genetics
  • Escherichia coli / growth & development
  • Escherichia coli / metabolism*
  • Feces / microbiology
  • Gastrointestinal Microbiome
  • Inflammation
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / physiology*
  • Male
  • Methylamines / blood
  • Methylamines / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism
  • Nitrates / metabolism
  • Obesity
  • Oxygen Consumption

Substances

  • Methylamines
  • Nitrates
  • trimethyloxamine
  • Choline