[PDF][PDF] Mapping interactions of microbial metabolites with human G-protein-coupled receptors

DA Colosimo, JA Kohn, PM Luo, FJ Piscotta, SM Han… - Cell host & …, 2019 - cell.com
DA Colosimo, JA Kohn, PM Luo, FJ Piscotta, SM Han, AJ Pickard, A Rao, JR Cross
Cell host & microbe, 2019cell.com
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 …
Summary
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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