TY - JOUR
T1 - Role of rsbU and Staphyloxanthin in phagocytosis and intracellular growth of staphylococcus aureus in human macrophages and endothelial cells
AU - Olivier, Aurélie C.
AU - Lemaire, Sandrine
AU - Van Bambeke, Françoise
AU - Tulkens, Paul M.
AU - Oldfield, Eric
N1 - Funding Information:
Received 24 February 2009; accepted 2 June 2009; electronically published 8 October 2009. Potential conflicts of interest: none reported. Financial support: Belgian Fonds de la Recherche Scientifique Médicale (grant 3.4.597.06); US Public Health Service (National Institutes of Health grant AI074233). Reprints or correspondence: Prof P. M. Tulkens, Université catholique de Louvain, 7370 ave Mounier 73, B-1200 Brussels, Belgium ([email protected]).
PY - 2009/11
Y1 - 2009/11
N2 - 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.
AB - 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.
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U2 - 10.1086/606012
DO - 10.1086/606012
M3 - Article
C2 - 19817587
AN - SCOPUS:72849109457
SN - 0022-1899
VL - 200
SP - 1367
EP - 1370
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 9
ER -