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Bifidobacterial carbohydrate/nucleoside metabolism enhances oxidative phosphorylation in white adipose tissue to protect against diet-induced obesity

DC Field Value Language
dc.contributor.authorKim, Gihyeon-
dc.contributor.authorYoon, Youngmin-
dc.contributor.authorPark, Jin Ho-
dc.contributor.authorPark, Jae Won-
dc.contributor.authorNoh, Myung-guin-
dc.contributor.authorKim, Hyun-
dc.contributor.authorPark, Changho-
dc.contributor.authorKwon, Hyuktae-
dc.contributor.authorPark, Jeong-hyeon-
dc.contributor.authorKim, Yena-
dc.contributor.authorSohn, Jinyoung-
dc.contributor.authorPark, Shinyoung-
dc.contributor.authorKim, Hyeonhui-
dc.contributor.authorIm, Sun-Kyoung-
dc.contributor.authorKim, Yeongmin-
dc.contributor.authorChung, Ha Yung-
dc.contributor.authorNam, Myung Hee-
dc.contributor.authorKwon, Jee Young-
dc.contributor.authorKim, Il Yong-
dc.contributor.authorKim, Yong Jae-
dc.contributor.authorBaek, Ji Hyeon-
dc.contributor.authorKim, Hak Su-
dc.contributor.authorWeinstock, George M.-
dc.contributor.authorCho, Belong-
dc.contributor.authorLee, Charles-
dc.contributor.authorFang, Sungsoon-
dc.contributor.authorPark, Hansoo-
dc.contributor.authorSeong, Je Kyung-
dc.date.accessioned2022-12-23T08:33:04Z-
dc.date.available2022-12-23T17:35:22Z-
dc.date.issued2022-11-04-
dc.identifier.citationMicrobiome, 10(1):188ko_KR
dc.identifier.issn2049-2618-
dc.identifier.urihttps://doi.org/10.1186/s40168-022-01374-0-
dc.identifier.urihttps://hdl.handle.net/10371/187337-
dc.description.abstractBackground
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.
ko_KR
dc.description.sponsorshipThis work was supported by the Korea Mouse Phenotyping Project (2013M3A9D5072550 and 2016M3A9D5A01952417) to J.K.S.; National Research Foundation of Korea (NRF) grant funded by the Korea government (NRF-2022M3H9A1080455) in 2022, and Bio and Medical Technology Development Program(NRF-2017M3A9F3046536) from the Ministry of Science and ICT, Korean Government, a GIST Research Institute (GRI) grand, funded by the GIST in 2021 and 2022 to H.P.; Bio and Medical Technology Development Program (NRF-2017M3A9F3046538), Korea Health Technology R&D Project (HI18C0012) from the Ministry of Health & Welfare and a faculty research grant from the Yonsei University College of Medicine (6-2018-0098) to S.F.ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.titleBifidobacterial carbohydrate/nucleoside metabolism enhances oxidative phosphorylation in white adipose tissue to protect against diet-induced obesityko_KR
dc.typeArticleko_KR
dc.identifier.doi10.1186/s40168-022-01374-0ko_KR
dc.citation.journaltitleMicrobiomeko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2022-11-06T04:14:57Z-
dc.citation.number1ko_KR
dc.citation.startpage188ko_KR
dc.citation.volume10ko_KR
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