Systematic screening of tryptophan metabolism identifies site- and microbial-specific signatures of tryptophan utilization in experimental colitis

Authors:
  • AAAbrar I Alsaadi
    Abrar I Alsaadi
  • DHDanielle Mm Harris
    Danielle Mm Harris
  • MYMeiping Yu
    Meiping Yu
  • TMTaous Mekdoud
    Taous Mekdoud
  • JBJohanna Bornhäuser
    Johanna Bornhäuser
  • ESEva Springer
    Eva Springer
  • CGClara Gilloteau
    Clara Gilloteau
  • APAnant A. Pothakamury
    Anant A. Pothakamury
  • JSJaclyn D. Smith
    Jaclyn D. Smith
  • BJBrenita C. Jenkins
    Brenita C. Jenkins
Preprint
Publisher website
Google Scholar
Abstract
Background: Altered tryptophan (Trp) metabolism and disrupted nicotinamide adenine dinucleotide (NAD⁺) synthesis are hallmarks of IBD, yet how intestinal microbiota contribute to these metabolic shifts during intestinal inflammation remains poorly understood. Methods: We used targeted metabolomics to systematically profile Trp- and NAD⁺-related metabolites across multiple biological compartments – including tissues, luminal contents, stool, and serum – in mice treated with dextran sulfate sodium (DSS) alone or in combination with a broad-spectrum antibiotic (ABX) cocktail. Results: Microbial depletion significantly attenuated colitis and increased host Trp bioavailability, implicating the gut microbiota as a competitive Trp consumer. In DSS colitis, Trp degradation along the kynurenine pathway (KP) was exaggerated but blocked at the key KP enzyme quinolinate phosphoribosyltransferase (QPRT), resulting in mucosal NAD(H) depletion. ABX co-treatment normalized metabolite conversion along the KP and restored mucosal NAD(H) levels, revealing a dual role of the gut microbiota during colitis: while they compete with the host for Trp utilization, they simultaneously shape host KP regulation and NAD⁺ de novo synthesis, supporting host energy homeostasis. Conclusion: Our findings demonstrate that mucosal NAD⁺ de novo synthesis is a microbially regulated metabolic process that alleviates intestinal inflammation and may represent a novel therapeutic target in IBD through modulation of the gut microbiota or their metabolites.

This publication has 66 references indexed in Scilit: