Bifidobacterial carbohydrate/nucleoside metabolism enhances oxidative phosphorylation in white adipose tissue to protect against diet-induced obesity
Gihyeon Kim,
Youngmin Yoon,
Jin Ho Park,
Jae Won Park,
Myung-guin Noh,
Hyun Kim,
Changho Park,
Hyuktae Kwon,
Jeong-hyeon Park,
Yena Kim,
Jinyoung Sohn,
Shinyoung Park,
Hyeonhui Kim,
Sun-Kyoung Im,
Yeongmin Kim,
Ha Yung Chung,
Myung Hee Nam,
Jee Young Kwon,
Il Yong Kim,
Yong Jae Kim,
Ji Hyeon Baek,
Hak Su Kim,
George M. Weinstock,
Belong Cho,
Charles Lee,
Sungsoon Fang,
Hansoo Park,
Je Kyung Seong
Affiliations
Gihyeon Kim
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST)
Youngmin Yoon
Division of Nephrology, Department of Medicine, Chosun University Hospital, Chosun University School of Medicine
Jin Ho Park
Department of Family Medicine, Seoul National University Hospital, Seoul National University College of Medicine
Jae Won Park
Genome and Company
Myung-guin Noh
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST)
Hyun Kim
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST)
Changho Park
Genome and Company
Hyuktae Kwon
Department of Family Medicine, Seoul National University Hospital, Seoul National University College of Medicine
Jeong-hyeon Park
Genome and Company
Yena Kim
Genome and Company
Jinyoung Sohn
Genome and Company
Shinyoung Park
Genome and Company
Hyeonhui Kim
Graduate school of Medical Science, Brain Korea 21 Project, Severance Biomedical Science Institute, Gangnam Severance Hospital, Yonsei University College of Medicine
Sun-Kyoung Im
Graduate school of Medical Science, Brain Korea 21 Project, Severance Biomedical Science Institute, Gangnam Severance Hospital, Yonsei University College of Medicine
Yeongmin Kim
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST)
Ha Yung Chung
Korea Basic Science Institute, Seoul Center
Myung Hee Nam
Korea Basic Science Institute, Seoul Center
Jee Young Kwon
The Jackson Laboratory for Genomic Medicine
Il Yong Kim
Laboratory of Developmental Biology and Genomics, BK21 Plus Program for Advanced Veterinary Science and Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University
Yong Jae Kim
Korea Mouse Phenotyping Center, Seoul National University
Ji Hyeon Baek
Korea Mouse Phenotyping Center, Seoul National University
Hak Su Kim
Korea Mouse Phenotyping Center, Seoul National University
George M. Weinstock
The Jackson Laboratory for Genomic Medicine
Belong Cho
Department of Family Medicine, Seoul National University Hospital, Seoul National University College of Medicine
Charles Lee
The Jackson Laboratory for Genomic Medicine
Sungsoon Fang
Graduate school of Medical Science, Brain Korea 21 Project, Severance Biomedical Science Institute, Gangnam Severance Hospital, Yonsei University College of Medicine
Hansoo Park
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST)
Je Kyung Seong
Laboratory of Developmental Biology and Genomics, BK21 Plus Program for Advanced Veterinary Science and Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University
Abstract Background Comparisons of the gut microbiome of lean and obese humans have revealed that obesity is associated with the gut microbiome plus changes in numerous environmental factors, including high-fat diet (HFD). Here, we report that two species of Bifidobacterium are crucial to controlling metabolic parameters in the Korean population. Results Based on gut microbial analysis from 99 Korean individuals, we observed the abundance of Bifidobacterium longum and Bifidobacterium bifidum was markedly reduced in individuals with increased visceral adipose tissue (VAT), body mass index (BMI), blood triglyceride (TG), and fatty liver. Bacterial transcriptomic analysis revealed that carbohydrate/nucleoside metabolic processes of Bifidobacterium longum and Bifidobacterium bifidum were associated with protecting against diet-induced obesity. Oral treatment of specific commercial Bifidobacterium longum and Bifidobacterium bifidum enhanced bile acid signaling contributing to potentiate oxidative phosphorylation (OXPHOS) in adipose tissues, leading to reduction of body weight gain and improvement in hepatic steatosis and glucose homeostasis. Bifidobacterium longum or Bifidobacterium bifidum manipulated intestinal sterol biosynthetic processes to protect against diet-induced obesity in germ-free mice. Conclusions Our findings support the notion that treatment of carbohydrate/nucleoside metabolic processes-enriched Bifidobacterium longum and Bifidobacterium bifidum would be a novel therapeutic strategy for reprograming the host metabolic homeostasis to protect against metabolic syndromes, including diet-induced obesity. Video Abstract