4.7 Article

Mapping Interactions of Microbial Metabolites with Human G-Protein-Coupled Receptors

Journal

CELL HOST & MICROBE
Volume 26, Issue 2, Pages 273-+

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2019.07.002

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Funding

  1. Bill and Melinda Gates Foundation [OPP1168674]
  2. National Institutes of Health [5R01AT009562-02]
  3. Bill and Melinda Gates Foundation [OPP1168674] Funding Source: Bill and Melinda Gates Foundation

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Despite evidence linking the human microbiome to health and disease, how the microbiota affects human physiology remains largely unknown. Microbiota-encoded metabolites are expected to play an integral role in human health. Therefore, assigning function to these metabolites is critical to understanding these complex interactions and developing microbiota-inspired therapies. Here, we use large-scale functional screening of molecules produced by individual members of a simplified human microbiota to identify bacterial metabolites that agonize G-protein-coupled receptors (GPCRs). Multiple metabolites, including phenylpropanoic acid, cadaverine, 9-10-methylenehexadecanoic acid, and 12-methyltetradecanoic acid, were found to interact with GPCRs associated with diverse functions within the nervous and immune systems, among others. Collectively, these metabolite-receptor pairs indicate that diverse aspects of human health are potentially modulated by structurally simple metabolites arising from primary bacterial metabolism.

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