The secreted proteases suppress the virulence of USA300 by shaping the extracellular proteome.

Surface-located and secreted virulence factors of the Gram-positive bacterial pathogen are key drivers for infection of the human host. Proteolytic enzymes may contribute to virulence by breaking primary barriers and host immune defenses. Therefore, the objective of our study was to chart the contributions of different proteases to virulence, and to assess their roles in shaping the staphylococcal surface proteome (the "surfacome") and extracellular proteome (the "secretome"). To this end, we applied 12 protease mutants of the USA300 lineage. Four mutants lacking the metalloprotease aureolysin (Aur), the cysteine proteases staphopain A (ScpA) and SspB, or the serine protease SspA displayed enhanced cytotoxicity toward human lung epithelial cells, showing that they serve to suppress virulence. Profiling of the surfacomes and secretomes of the four mutants allowed correlation of their increased cytotoxicity to altered virulence factor profiles. Furthermore, enhanced levels of virulence factors were detected in the mutants' surfacomes, which was shown to be relevant as all four mutants displayed enhanced lung epithelial cell invasion. Enhanced levels of cytoplasmic and membrane proteins in the mutant's surfacomes showed that Aur, ScpA, SspA and SspB set limits to autolysis by reducing the levels of peptidoglycan hydrolases. We conclude that Aur, ScpA, SspA and SspB have key roles in shaping the surfacome and secretome of , thereby controlling the virulence of this major pathogen. This implies that novel antimicrobial agents or vaccines should not target these proteases.