作者
Ken Liu,Joshua A. Owens,Bejan Saeedi,Catherine E. Cohen,Moriah P. Bellissimo,Crystal Naudin,Trevor Darby,Samuel Druzak,Kristal Maner-Smith,Michael C. Orr,Xin Hu,Jolyn Fernandes,Mary Catherine Camacho,Sarah Hunter-Chang,David VanInsberghe,Chunyu Ma,Thota Ganesh,Samantha M. Yeligar,Karan Uppal,Young‐Mi Go,Jessica A. Alvarez,Miriam B. Vos,Thomas R. Ziegler,Michael H. Woodworth,Colleen S. Kraft,Rheinallt M. Jones,Eric A. Ortlund,Andrew S. Neish,Dean P. Jones
摘要
Obesity and obesity-related metabolic disorders are linked to the intestinal microbiome. However, the causality of changes in the microbiome–host interaction affecting energy metabolism remains controversial. Here, we show the microbiome-derived metabolite δ-valerobetaine (VB) is a diet-dependent obesogen that is increased with phenotypic obesity and is correlated with visceral adipose tissue mass in humans. VB is absent in germ-free mice and their mitochondria but present in ex-germ-free conventionalized mice and their mitochondria. Mechanistic studies in vivo and in vitro show VB is produced by diverse bacterial species and inhibits mitochondrial fatty acid oxidation through decreasing cellular carnitine and mitochondrial long-chain acyl-coenzyme As. VB administration to germ-free and conventional mice increases visceral fat mass and exacerbates hepatic steatosis with a western diet but not control diet. Thus, VB provides a molecular target to understand and potentially manage microbiome–host symbiosis or dysbiosis in diet-dependent obesity. Delta-valerobetaine is a microbiome-derived metabolite that correlates with obesity-related phenotypes in humans, and exacerbates diet-induced obesity in mice.