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Journal article

Human gut microbes impact host serum metabolome and insulin sensitivity

From

Department of Systems Biology, Technical University of Denmark1

Steno Diabetes Centre2

Vrije Universiteit Brussel3

Technical Information Center of Denmark, Technical University of Denmark4

University of Turku5

Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark6

Integrative Systems Biology, Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark7

Örebro University8

University of Copenhagen9

European Molecular Biology Laboratory10

Université Paris-Saclay11

KU Leuven12

VTT Technical Research Centre of Finland Ltd.13

...and 3 more

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.

Language: English
Publisher: Nature Publishing Group
Year: 2016
Pages: 376-381
Journal subtitle: International Weekly Journal of Science
ISSN: 14764687 and 00280836
Types: Journal article
DOI: 10.1038/nature18646
ORCIDs: Nielsen, Henrik Bjørn , Pedersen, Susanne Brix , 0000-0002-2066-7895 , 0000-0001-6991-0828 , 0000-0002-0886-9101 , 0000-0002-6024-0917 , 0000-0001-8748-3831 , 0000-0003-0316-5866 and 0000-0002-3321-3972

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