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. © 2009 by the Infectious Diseases Society of America.
CITATION STYLE
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. Journal of Infectious Diseases, 200(9), 1367–1370. https://doi.org/10.1086/606012
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