FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Zhao, D., Shiga, R.T., Song, Z., Shu, R., Loo, L., Wong, A.C.N. (2025). Microbiome drives age-dependent shifts in brain transcriptomic programs at the single-cell level in Drosophila.  NPJ Biofilms Microbiomes 11(1): 162.
FlyBase ID
FBrf0263095
Publication Type
Research paper
Abstract
The gut microbiome plays a critical role in brain function and the brain-gut axis, yet its cellular and molecular mechanisms remain unclear. Here, we present the first comprehensive single-cell transcriptomic atlas of brain cells from adult Drosophila melanogaster raised under axenic and microbiome-associated conditions, spanning young and old ages. Profiling 34,427 cells across 101 clusters, we annotated 56 cell types and identified cell type-specific gene signatures influenced by the microbiome. Transcriptional shifts were most pronounced in old flies, with glial cells and dopaminergic neurons among the most microbiome-responsive cell types. Differentially expressed genes (DEGs) were enriched in pathways related to mitochondrial activity, energy metabolism, and Notch signaling. We also quantified age-associated changes in the gut microbiome, observing reduced Acetobacter dominance and increased microbial diversity that corresponded with heightened brain transcriptional responses. These findings illuminate the cell type-specific impacts of the microbiome on brain gene expression and lay the groundwork for understanding the molecular underpinnings of the microbiome-gut-brain axis.
PubMed ID
PubMed Central ID
PMC12344059 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    NPJ Biofilms Microbiomes
    Title
    NPJ biofilms and microbiomes
    ISBN/ISSN
    2055-5008
    Data From Reference