• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

Gut Microbes . Shotgun metagenomics and systemic targeted metabolomics highlight indole-3-propionic acid as a protective gut microbial metabolite ag

tetano

Editor, Senior Moderator
Gut Microbes


. 2024 Jan-Dec;16(1):2325067.
doi: 10.1080/19490976.2024.2325067. Epub 2024 Mar 6. Shotgun metagenomics and systemic targeted metabolomics highlight indole-3-propionic acid as a protective gut microbial metabolite against influenza infection

Séverine Heumel[SUP] 1 [/SUP], Vinícius de Rezende Rodovalho[SUP] 2 [/SUP], Charlotte Urien[SUP] 3 [/SUP], Florian Specque[SUP] 4 [/SUP], Patrícia Brito Rodrigues[SUP] 1 2 [/SUP], Cyril Robil[SUP] 1 [/SUP], Lou Delval[SUP] 1 [/SUP], Valentin Sencio[SUP] 1 [/SUP], Amandine Descat[SUP] 5 [/SUP], Lucie Deruyter[SUP] 1 [/SUP], Stéphanie Ferreira[SUP] 3 [/SUP], Marina Gomes Machado[SUP] 1 [/SUP], Adeline Barthelemy[SUP] 1 [/SUP], Fabiola Silva Angulo[SUP] 1 [/SUP], Joel T Haas[SUP] 6 [/SUP], Jean François Goosens[SUP] 5 [/SUP], Isabelle Wolowczuk[SUP] 1 [/SUP], Corinne Grangette[SUP] 1 [/SUP], Yves Rouillé[SUP] 1 [/SUP], Ghjuvan Grimaud[SUP] 4 [/SUP], Marie Lenski[SUP] 7 [/SUP], Benjamin Hennart[SUP] 7 [/SUP], Marco Aurélio Ramirez Vinolo[SUP] 2 [/SUP], François Trottein[SUP] 1 [/SUP]



Affiliations
Abstract

The gut-to-lung axis is critical during respiratory infections, including influenza A virus (IAV) infection. In the present study, we used high-resolution shotgun metagenomics and targeted metabolomic analysis to characterize influenza-associated changes in the composition and metabolism of the mouse gut microbiota. We observed several taxonomic-level changes on day (D)7 post-infection, including a marked reduction in the abundance of members of the Lactobacillaceae and Bifidobacteriaceae families, and an increase in the abundance of Akkermansia muciniphila. On D14, perturbation persisted in some species. Functional scale analysis of metagenomic data revealed transient changes in several metabolic pathways, particularly those leading to the production of short-chain fatty acids (SCFAs), polyamines, and tryptophan metabolites. Quantitative targeted metabolomics analysis of the serum revealed changes in specific classes of gut microbiota metabolites, including SCFAs, trimethylamine, polyamines, and indole-containing tryptophan metabolites. A marked decrease in indole-3-propionic acid (IPA) blood level was observed on D7. Changes in microbiota-associated metabolites correlated with changes in taxon abundance and disease marker levels. In particular, IPA was positively correlated with some Lactobacillaceae and Bifidobacteriaceae species (Limosilactobacillus reuteri, Lactobacillus animalis) and negatively correlated with Bacteroidales bacterium M7, viral load, and inflammation markers. IPA supplementation in diseased animals reduced viral load and lowered local (lung) and systemic inflammation. Treatment of mice with antibiotics targeting IPA-producing bacteria before infection enhanced viral load and lung inflammation, an effect inhibited by IPA supplementation. The results of this integrated metagenomic-metabolomic analysis highlighted IPA as an important contributor to influenza outcomes and a potential biomarker of disease severity.

Keywords: Influenza; disease severity; gut microbiota; indole-3-propionic acid; metabolomics; shotgun metagenomics.

 
Back
Top Bottom