4.8 Article

A gut bacterial pathway metabolizes aromatic amino acids into nine circulating metabolites

Journal

NATURE
Volume 551, Issue 7682, Pages 648-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nature24661

Keywords

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Funding

  1. National Institutes of Health NIDDK [R01-DK101674]
  2. NIH [DP2-OD006515, U19AI057229, U19AI100627, R33CA183654, R33CA0183692, R01GM10983601, R01CA184968, R01CA19665701, R21CA183660, R01NS08953301, 5UH2AR067676, R01HL120724, DP5-OD023056]
  3. FDA [BAA-12-00118]
  4. Department of Defence [OC110674, W81XWH-14-1-0 180]
  5. Gates Foundation [OPP1113682, DP1 DK113598, R01 DK110174]
  6. HHMI-Simons Faculty Scholars Award
  7. Byers Award in Basic Science
  8. David and Lucile Packard Foundation
  9. BASF research grant
  10. Burroughs Wellcome Investigators in the Pathogenesis of Infectious Disease Awards
  11. NIH postdoctoral NRSA [T32-AI007328]
  12. National Science Foundation [DGE-114747]

Ask authors/readers for more resources

The human gut microbiota produces dozens of metabolites that accumulate in the bloodstream(1,2), where they can have systemic effects on the host. Although these small molecules commonly reach concentrations similar to those achieved by pharmaceutical agents, remarkably little is known about the microbial metabolic pathways that produce them. Here we use a combination of genetics and metabolic profiling to characterize a pathway from the gut symbiont Clostridium sporogenes that generates aromatic amino acid metabolites. Our results reveal that this pathway produces twelve compounds, nine of which are known to accumulate in host serum. All three aromatic amino acids (tryptophan, phenylalanine and tyrosine) serve as substrates for the pathway, and it involves branching and alternative reductases for specific intermediates. By genetically manipulating C. sporogenes, we modulate serum levels of these metabolites in gnotobiotic mice, and show that in turn this affects intestinal permeability and systemic immunity. This work has the potential to provide the basis of a systematic effort to engineer the molecular output of the gut bacterial community.

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