Abstract
How virus-host cell interactions and innate immune antagonism shape neurotropic infection dynamics across diverse brain cell types is largely unknown. To "unmask" and study how innate immune inhibition affects cell-type-specific transcriptional regulation of the human and viral genome, we perform single-cell RNA sequencing of human brain cell co-cultures, comparing an isolate of rabies virus (RABV) to its mutant incapable of antagonizing interferon- and nuclear factor (NF)-κB-dependent responses. RABV gene expression is shaped by host cell type. RABV induces small-scale, cell-type-conserved transcriptional programs that likely support infection by (1) hijacking negative transcriptional feedback of pro-viral factors while (2) reducing anti-viral RNAs. Unexpectedly, disinhibited innate immune signaling increases RABV transcription, most strikingly in an infection-independent "pro-viral" astrocyte subpopulation. Further analysis suggests that pro-viral-like astrocytes are a rare subtype in the human brain and are primed to protect the brain during viral infection in concert with interferon-sensitive microglia recalcitrant to infection.