FB2026_03 , released September 17, 2026
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Castells-Nobau, A., Puig, I., Motger-Albertí, A., de la Vega-Correa, L., Rosell-Díaz, M., Arnoriaga-Rodríguez, M., Escrichs, A., Garre-Olmo, J., Puig, J., Ramos, R., Ramió-Torrentà, L., Pérez-Brocal, V., Moya, A., Pamplona, R., Jové, M., Sol, J., Martin-Garcia, E., Martinez-Garcia, M., Deco, G., Maldonado, R., Fernández-Real, J.M., Mayneris-Perxachs, J. (2024). Microviridae bacteriophages influence behavioural hallmarks of food addiction via tryptophan and tyrosine signalling pathways.  Nat Metab 6(11): 2157--2186.
FlyBase ID
FBrf0261009
Publication Type
Research paper
Abstract
Food addiction contributes to the obesity pandemic, but the connection between how the gut microbiome is linked to food addiction remains largely unclear. Here we show that Microviridae bacteriophages, particularly Gokushovirus WZ-2015a, are associated with food addiction and obesity across multiple human cohorts. Further analyses reveal that food addiction and Gokushovirus are linked to serotonin and dopamine metabolism. Mice receiving faecal microbiota and viral transplantation from human donors with the highest Gokushovirus load exhibit increased food addiction along with changes in tryptophan, serotonin and dopamine metabolism in different regions of the brain, together with alterations in dopamine receptors. Mechanistically, targeted tryptophan analysis shows lower anthranilic acid (AA) concentrations associated with Gokushovirus. AA supplementation in mice decreases food addiction and alters pathways related to the cycle of neurotransmitter synthesis release. In Drosophila, AA regulates feeding behaviour and addiction-like ethanol preference. In summary, this study proposes that bacteriophages in the gut microbiome contribute to regulating food addiction by modulating tryptophan and tyrosine metabolism.
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat Metab
    Title
    Nature metabolism
    ISBN/ISSN
    2522-5812
    Data From Reference
    Chemicals (1)
    Genes (1)
    Human Disease Models (1)