Abstract
The native microbiome influences numerous host processes, including neurological function. However, its impacts on diverse brain cell types remain poorly understood. Here, we performed single-nucleus RNA sequencing on the hippocampus of wild-type, germ-free mice, revealing the microbiome-dependent transcriptional landscape across all major neural cell types. We found conserved impacts on key adaptive immune and neurodegenerative transcriptional pathways. Mono-colonization with select indigenous microbes identified organism-specific effects on brain myeloid cell transcriptional state. Escherichia coli colonization induced a distinct myeloid cell activation state, increased brain-resident CD8(+) T cells, and shaped amyloid phagocytic capacity, suggesting heightened disease susceptibility. Finally, E. coli-exposed 5xFAD mice displayed exacerbated cognitive decline and amyloid pathology, demonstrating the sufficiency of intestinal E. coli to worsen Alzheimer's disease-relevant outcomes. Together, these results emphasize the broad, species-specific, microbiome-dependent consequences on neural cell states and highlight the capacity of specific microbes to modulate disease susceptibility.