4.8 Article

Human gut microbes impact host serum metabolome and insulin sensitivity

Journal

NATURE
Volume 535, Issue 7612, Pages 376-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/nature18646

Keywords

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Funding

  1. European Community [HEALTH-F4-2007-201052]
  2. Lundbeck Foundation Centre for Applied Medical Genomics in Personalized Disease Prediction, Prevention and Care (LuCamp), Metagenopolis grant [ANR-11-DPBS-0001, HEALTH-F4-2012-305312]
  3. Rega institute for Medical Research, KU Leuven
  4. Agency for Innovation by Science and Technology (IWT) [267139]
  5. Fund for Scientific Research Flanders (FWO)
  6. Academy of Finland (Centre of Excellence in Molecular Systems Immunology and Physiology Research) [250114]
  7. EU FP7 Project TORNADO [222720]
  8. European Union [600375]
  9. Innovative Medicines Initiative Joint Undertaking from the European Union [115317]

Ask authors/readers for more resources

Insulin resistance is a forerunner state of ischaemic cardiovascular disease and type 2 diabetes. Here we show how the human gut microbiome impacts the serum metabolome and associates with insulin resistance in 277 non-diabetic Danish individuals. The serum metabolome of insulin-resistant individuals is characterized by increased levels of branched-chain amino acids (BCAAs), which correlate with a gut microbiome that has an enriched biosynthetic potential for BCAAs and is deprived of genes encoding bacterial inward transporters for these amino acids. Prevotella copri and Bacteroides vulgatus are identified as the main species driving the association between biosynthesis of BCAAs and insulin resistance, and in mice we demonstrate that P. copri can induce insulin resistance, aggravate glucose intolerance and augment circulating levels of BCAAs. Our findings suggest that microbial targets may have the potential to diminish insulin resistance and reduce the incidence of common metabolic and cardiovascular disorders.

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