Intracellular persistence of in endothelial cells is promoted by the absence of phenol-soluble modulins.

A large proportion of clinical isolates that carry an inactive Agr system are associated with persistent infection that is difficult to treat. Once is inside the bloodstream, it can cross the endothelial barrier and invade almost every organ in the human body. Endothelial cells can either be lysed by this pathogen or they serve as a niche for its intracellular long-term survival. Following phagocytosis, several vesicles such as phagosomes and autophagosomes, target intracellular for elimination. can escape from these vesicles into the host cytoplasm through the activation of phenol-soluble modulins (PSMs) αβ. Thereafter, it replicates and lyses the host cell to disseminate to adjacent tissues. Herein we demonstrate that staphylococcal strains which lack the expression of PSMs employ an alternative pathway to better persist within endothelial cells. The intracellular survival of is associated with the co-localization of the autophagy marker LC3. In cell culture infection models, we found that the absence of decreased the host cell lysis and increased staphylococcal long-term survival. This study explains the positive selection of -negative strains that lack the expression of in chronic infection due to their advantage in surviving and evading the clearance system of the host.