In Staphylococcus aureus, rsbU down-regulates agr and stimulates production of staphyloxanthin (STX), an antioxidant that may contribute to intracellular survival after phagocytosis. Using isogenic rsbU(-) and rsbU(+) strains, we show that rsbU causes increased internalization and intracellular growth in both THP-1 macrophages and human umbilical vein endothelial cells (more so for the latter) without change in subcellular localization and that inhibition of STX biosynthesis markedly reduces intracellular growth of the rsbU(+) strain (and of clinical isolates, including USA300; tested with macrophages only) without affecting internalization. Thus, rsbU is important for uptake and for STX biosynthesis and is critical for intracellular multiplication of S. aureus.
Olivier, A. C., Lemaire, S., Van Bambeke, F., Tulkens, P. M., & Oldfield, E. (2009). Role of rsbU and staphyloxanthin in phagocytosis and intracellular growth of staphylococcus aureus in human macrophages and endothelial cells. The Journal of Infectious Diseases, 200(9), 1367-1370. https://doi.org/10.1086/606012 (Original work published 2009)