Integrative metagenomics and metabolomics reveal age-associated gut microbiota and metabolite alterations in a hamster model of COVID-19

Aging is a key contributor of morbidity and mortality during acute viral pneumonia. The potential role of age-associated dysbiosis on disease outcomes is still elusive. In the current study, we used high-resolution shotgun metagenomics and targeted metabolomics to characterize SARS-CoV-2-associated changes in the gut microbiota from young (2-month-old) and aged (22-month-old) hamsters, a valuable model of COVID-19. We show that age-related dysfunctions in the gut microbiota are linked to disease severity and long-term sequelae in older hamsters. Our data also reveal age-specific changes in the composition and metabolic activity of the gut microbiota during both the acute phase (day 7 post-infection, D7) and the recovery phase (D22) of infection. Aged hamsters exhibited the most notable shifts in gut microbiota composition and plasma metabolic profiles. Through an integrative analysis of metagenomics, metabolomics, and clinical data, we identified significant associations between bacterial taxa, metabolites and disease markers in the aged group. On D7 (high viral load and lung epithelial damage) and D22 (body weight loss and fibrosis), numerous amino acids, amino acid-related molecules, and indole derivatives were found to correlate with disease markers. In particular, a persistent decrease in phenylalanine, tryptophan, glutamic acid, and indoleacetic acid in aged animals positively correlated with poor recovery of body weight and/or lung fibrosis by D22. In younger hamsters, several bacterial taxa (<i>Eubacterium</i>, <i>Oscillospiraceae</i>, <i>Lawsonibacter</i>) and plasma metabolites (carnosine and cis-aconitic acid) were associated with mild disease outcomes. These findings support the need for age-specific microbiome-targeting strategies to more effectively manage acute viral pneumonia and long-term disease outcomes.

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Publication Details

Journal
Gut Microbes
Published
2025-04-02
DOI
https://doi.org/10.1080/19490976.2025.2486511
Citations
5
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
4.03

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article

Integrative metagenomics and metabolomics reveal age-associated gut microbiota and metabolite alterations in a hamster model of COVID-19

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5 citations
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article

Integrative metagenomics and metabolomics reveal age-associated gut microbiota and metabolite alterations in a hamster model of COVID-19

Patrícia Brito Rodrigues, Cyril Robil, Arnaud Machelart, Vinícius de Rezende Rodovalho, Nicolás Benech, Florence Maurier, Marco Aurélio Ramirez Vinolo, Amandine Descat, Delphine Beury, Lou Delval, François Trottein, Valentin Sencio, Joel T. Haas, Isabelle Wolowczuk, Philippe Gosset, David Hot, Marybeth Creskey, Fabiola Silva, Harry Sokol, Jean François Goosens, Xu Zhang
article en
5 citations

Abstract

Aging is a key contributor of morbidity and mortality during acute viral pneumonia. The potential role of age-associated dysbiosis on disease outcomes is still elusive. In the current study, we used high-resolution shotgun metagenomics and targeted metabolomics to characterize SARS-CoV-2-associated changes in the gut microbiota from young (2-month-old) and aged (22-month-old) hamsters, a valuable model of COVID-19. We show that age-related dysfunctions in the gut microbiota are linked to disease severity and long-term sequelae in older hamsters. Our data also reveal age-specific changes in the composition and metabolic activity of the gut microbiota during both the acute phase (day 7 post-infection, D7) and the recovery phase (D22) of infection. Aged hamsters exhibited the most notable shifts in gut microbiota composition and plasma metabolic profiles. Through an integrative analysis of metagenomics, metabolomics, and clinical data, we identified significant associations between bacterial taxa, metabolites and disease markers in the aged group. On D7 (high viral load and lung epithelial damage) and D22 (body weight loss and fibrosis), numerous amino acids, amino acid-related molecules, and indole derivatives were found to correlate with disease markers. In particular, a persistent decrease in phenylalanine, tryptophan, glutamic acid, and indoleacetic acid in aged animals positively correlated with poor recovery of body weight and/or lung fibrosis by D22. In younger hamsters, several bacterial taxa (<i>Eubacterium</i>, <i>Oscillospiraceae</i>, <i>Lawsonibacter</i>) and plasma metabolites (carnosine and cis-aconitic acid) were associated with mild disease outcomes. These findings support the need for age-specific microbiome-targeting strategies to more effectively manage acute viral pneumonia and long-term disease outcomes.

Gut MicrobesVol. 17(1)
Health Canada (CA), Centre National de la Recherche Scientifique (FR), University of Ottawa (CA), Inserm (FR), Universidade Estadual de Campinas (UNICAMP) (BR), AgroParisTech (FR), Université de Lille (FR), Université Paris-Saclay (FR), Institut Pasteur de Lille (FR), Microbiologie de l’alimentation au service de la santé (FR), Centre Hospitalier Universitaire de Lille (FR), Sorbonne Université (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Assistance Publique – Hôpitaux de Paris (FR), Center for Infection and Immunity of Lille (FR), Hospices Civils de Lyon (FR), Fédération Hospitalo-Universitaire, Paris Center for Microbiome Medicine (FR), Centre de Recherche Saint-Antoine (FR)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Fundação de Amparo à Pesquisa do Estado de São Paulo, Centre National de la Recherche Scientifique
Good health and well-being
Openalex Percentile: Top 7%
Gut microbiota and health
4.03
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