Gut microbial carbohydrate metabolism contributes to insulin resistance

Tadashi Takeuchi(RIKEN Center for Integrative Medical Sciences), Tetsuya Kubota(Toho University), Yumiko Nakanishi(RIKEN Center for Integrative Medical Sciences), Hiroshi Tsugawa(RIKEN Center for Sustainable Resource Science), Wataru Suda(RIKEN Center for Integrative Medical Sciences), Andrew Tae-Jun Kwon(RIKEN Center for Integrative Medical Sciences), Junshi Yazaki(RIKEN Center for Integrative Medical Sciences), Kazutaka Ikeda(Kazusa DNA Research Institute), Shino Nemoto(RIKEN Center for Integrative Medical Sciences), Yoshiki Mochizuki(RIKEN Center for Integrative Medical Sciences), Toshimori Kitami(RIKEN Center for Integrative Medical Sciences), Katsuyuki Yugi(Keio University Shonan Fujisawa), Yoshiko Mizuno(Development Bank of Japan), Nobutake Yamamichi(University of Tokyo Hospital), Tsutomu Yamazaki(International University of Health and Welfare), Iseki Takamoto(Tokyo Medical University Ibaraki Medical Center), Naoto Kubota(The University of Tokyo), Takashi Kadowaki(Toranomon Hospital), Erik Arner(RIKEN Center for Integrative Medical Sciences), Piero Carninci(Human Technopole), Osamu Ohara(Kazusa DNA Research Institute), Makoto Arita(Keio University), Masahira Hattori(RIKEN Center for Integrative Medical Sciences), Shigeo Koyasu(RIKEN Center for Integrative Medical Sciences), Hiroshi Ohno(Yokohama City University Medical Center)
Nature
August 30, 2023
Cited by 401Open Access
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Abstract

Abstract Insulin resistance is the primary pathophysiology underlying metabolic syndrome and type 2 diabetes 1,2 . Previous metagenomic studies have described the characteristics of gut microbiota and their roles in metabolizing major nutrients in insulin resistance 3–9 . In particular, carbohydrate metabolism of commensals has been proposed to contribute up to 10% of the host’s overall energy extraction 10 , thereby playing a role in the pathogenesis of obesity and prediabetes 3,4,6 . Nevertheless, the underlying mechanism remains unclear. Here we investigate this relationship using a comprehensive multi-omics strategy in humans. We combine unbiased faecal metabolomics with metagenomics, host metabolomics and transcriptomics data to profile the involvement of the microbiome in insulin resistance. These data reveal that faecal carbohydrates, particularly host-accessible monosaccharides, are increased in individuals with insulin resistance and are associated with microbial carbohydrate metabolisms and host inflammatory cytokines. We identify gut bacteria associated with insulin resistance and insulin sensitivity that show a distinct pattern of carbohydrate metabolism, and demonstrate that insulin-sensitivity-associated bacteria ameliorate host phenotypes of insulin resistance in a mouse model. Our study, which provides a comprehensive view of the host–microorganism relationships in insulin resistance, reveals the impact of carbohydrate metabolism by microbiota, suggesting a potential therapeutic target for ameliorating insulin resistance.


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