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Gut microbial carbohydrate metabolism contributes to insulin resistance

Author

Listed:
  • Tadashi Takeuchi

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Tetsuya Kubota

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Kanagawa Institute of Industrial Science and Technology
    The University of Tokyo
    The Institute for Medical Science Asahi Life Foundation)

  • Yumiko Nakanishi

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Kanagawa Institute of Industrial Science and Technology)

  • Hiroshi Tsugawa

    (RIKEN Center for Sustainable Resource Science (CSRS)
    RIKEN Center for Integrative Medical Sciences (IMS)
    Yokohama City University
    Tokyo University of Agriculture and Technology)

  • Wataru Suda

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Andrew Tae-Jun Kwon

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Junshi Yazaki

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Kazutaka Ikeda

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Kazusa DNA Research Institute)

  • Shino Nemoto

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Yoshiki Mochizuki

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Toshimori Kitami

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Katsuyuki Yugi

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Keio University
    The University of Tokyo)

  • Yoshiko Mizuno

    (The University of Tokyo
    Development Bank of Japan)

  • Nobutake Yamamichi

    (The University of Tokyo Hospital)

  • Tsutomu Yamazaki

    (International University of Health and Welfare)

  • Iseki Takamoto

    (The University of Tokyo
    Tokyo Medical University Ibaraki Medical Center)

  • Naoto Kubota

    (The University of Tokyo)

  • Takashi Kadowaki

    (The University of Tokyo
    Toranomon Hospital)

  • Erik Arner

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Piero Carninci

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Fondazione Human Technopole)

  • Osamu Ohara

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Kazusa DNA Research Institute)

  • Makoto Arita

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Yokohama City University
    Keio University
    Keio University)

  • Masahira Hattori

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Shigeo Koyasu

    (RIKEN Center for Integrative Medical Sciences (IMS))

  • Hiroshi Ohno

    (RIKEN Center for Integrative Medical Sciences (IMS)
    Kanagawa Institute of Industrial Science and Technology
    Yokohama City University)

Abstract

Insulin resistance is the primary pathophysiology underlying metabolic syndrome and type 2 diabetes1,2. Previous metagenomic studies have described the characteristics of gut microbiota and their roles in metabolizing major nutrients in insulin resistance3–9. In particular, carbohydrate metabolism of commensals has been proposed to contribute up to 10% of the host’s overall energy extraction10, thereby playing a role in the pathogenesis of obesity and prediabetes3,4,6. 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.

Suggested Citation

  • Tadashi Takeuchi & Tetsuya Kubota & Yumiko Nakanishi & Hiroshi Tsugawa & Wataru Suda & Andrew Tae-Jun Kwon & Junshi Yazaki & Kazutaka Ikeda & Shino Nemoto & Yoshiki Mochizuki & Toshimori Kitami & Kats, 2023. "Gut microbial carbohydrate metabolism contributes to insulin resistance," Nature, Nature, vol. 621(7978), pages 389-395, September.
  • Handle: RePEc:nat:nature:v:621:y:2023:i:7978:d:10.1038_s41586-023-06466-x
    DOI: 10.1038/s41586-023-06466-x
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    Cited by:

    1. Diego E. Sastre & Nazneen Sultana & Marcos V. A. S. Navarro & Maros Huliciak & Jonathan Du & Javier O. Cifuente & Maria Flowers & Xu Liu & Pete Lollar & Beatriz Trastoy & Marcelo E. Guerin & Eric J. S, 2024. "Human gut microbes express functionally distinct endoglycosidases to metabolize the same N-glycan substrate," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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