Single-cell analysis of CX3CR1+cells reveal a pathogenic role for BIRC5+myeloid proliferating cells driven byStaphylococcus aureusleukotoxins

Abstract

AbstractOur previous studies identified a population of stem cell-like proliferating myeloid cells within inflamed tissues that could serve as a reservoir for tissue macrophages to adopt different activation states depending on the microenvironment. By lineage tracing cells derived from CX3CR1+precursors in mice during infection and profiling by scRNA-seq, here we identify a cluster of BIRC5+myeloid cells that expanded in the liver during either chronic infection with the parasiteSchistosoma mansonior the bacterial pathogenStaphylococcus aureus. In the absence of tissue damaging toxins,S. aureusinfection does not elicit these BIRC5+cells. Moreover, deletion of BIRC5 from CX3CR1 expressing cells results in improved survival duringS. aureusinfection. Hence, the combination of scRNA-Seq and genetic fate mapping CX3CR1+cells revealed a toxin dependent pathogenic role for BIRC5 in myeloid cells duringS. aureusinfection.