High-fat diet-induced colonocyte dysfunction escalates microbiota-derived trimethylamine N-oxide.
Woongjae YooJacob K ZiebaNora J FoegedingTeresa P TorresCatherine D SheltonNicolas G ShealyAustin J ByndlossStephanie A CevallosErik GertzConnor R TiffanyJulia D ThomasYael LitvakHenry NguyenErin E OlsanBrian J BennettJeffrey C RathmellAmy S MajorAndreas J BäumlerMariana X ByndlossPublished in: Science (New York, N.Y.) (2021)
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.
Keyphrases
- high fat diet
- insulin resistance
- high fat diet induced
- escherichia coli
- adipose tissue
- cardiovascular disease
- metabolic syndrome
- mouse model
- type diabetes
- skeletal muscle
- weight loss
- cell death
- nitric oxide
- south africa
- drinking water
- body mass index
- oxidative stress
- sensitive detection
- pseudomonas aeruginosa
- weight gain
- ulcerative colitis