Feeding diversified protein sources exacerbates hepatic insulin resistance via increased gut microbial branched-chain fatty acids and mTORC1 signaling in obese mice

Research output: Contribution to journalJournal articleResearchpeer-review

  • Choi, Beatrice
  • Noemie Daniel
  • Vanessa P. Houde
  • Adia Ouellette
  • Bruno Marcotte
  • Thibault V. Varin
  • Cecile Vors
  • Perrine Feutry
  • Olga Ilkayeva
  • Marcus Stahlman
  • Philippe St-Pierre
  • Fredrik Bäckhed
  • Angelo Tremblay
  • Phillip J. White
  • Andre Marette

Animal models of human diseases are classically fed purified diets that contain casein as the unique protein source. We show that provision of a mixed protein source mirroring that found in the western diet exacerbates diet-induced obesity and insulin resistance by potentiating hepatic mTORC1/S6K1 signaling as compared to casein alone. These effects involve alterations in gut microbiota as shown by fecal microbiota transplantation studies. The detrimental impact of the mixed protein source is also linked with early changes in microbial production of branched-chain fatty acids (BCFA) and elevated plasma and hepatic acylcarnitines, indicative of aberrant mitochondrial fatty acid oxidation. We further show that the BCFA, isobutyric and isovaleric acid, increase glucose production and activate mTORC1/S6K1 in hepatocytes. Our findings demonstrate that alteration of dietary protein source exerts a rapid and robust impact on gut microbiota and BCFA with significant consequences for the development of obesity and insulin resistance. Diet-induced changes in the microbiome have been associated with obesity. Here, using a mouse model, the authors show that a mixed protein source found in western diets exacerbates diet-induced obesity and insulin resistance by potentiating hepatic mTORC1/S6K1 signaling via microbial production of branched-chain fatty acids (BCFA).

Original languageEnglish
Article number3377
JournalNature Communications
Volume12
Number of pages16
ISSN2041-1723
DOIs
Publication statusPublished - 2021

    Research areas

  • PLASMA ACYLCARNITINES, METABOLISM, DIET, IDENTIFICATION, INFLAMMATION, ISOBUTYRATE, POPULATION, OXIDATION, GLUCOSE, THETA

ID: 274620338