Staphylococcus aureus regulates the expression and production of the staphylococcal superantigen-like secreted proteins in a Rot-dependent manner

被引:47
作者
Benson, Meredith A. [1 ]
Lilo, Sarit [1 ]
Wasserman, Gregory A. [2 ]
Thoendel, Matthew [3 ]
Smith, Amanda [1 ]
Horswill, Alexander R. [3 ]
Fraser, John [4 ,5 ]
Novick, Richard P. [1 ,6 ]
Shopsin, Bo [1 ,2 ]
Torres, Victor J. [1 ]
机构
[1] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Med, Div Infect Dis, New York, NY 10016 USA
[3] Univ Iowa, Dept Microbiol, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
[4] Univ Auckland, Sch Med Sci, Auckland 1, New Zealand
[5] Univ Auckland, Maurice Wilkins Ctr, Auckland 1, New Zealand
[6] NYU, Sch Med, Mol Pathogenesis Program, Skirball Inst Biomol Med, New York, NY 10016 USA
关键词
ACCESSORY GENE REGULATOR; FC-ALPHA-RI; METHICILLIN-RESISTANT; IN-VIVO; DIMINISHED VIRULENCE; BACTERIAL PATHOGENS; SIGNAL-TRANSDUCTION; GLOBAL REGULATION; AGR DYSFUNCTION; IMMUNE EVASION;
D O I
10.1111/j.1365-2958.2011.07720.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Staphylococcus aureus overproduces a subset of immunomodulatory proteins known as the staphylococcal superantigen-like proteins (Ssls) under conditions of pore-mediated membrane stress. In this study we demonstrate that overproduction of Ssls during membrane stress is due to the impaired activation of the two-component module of the quorum-sensing accessory gene regulator (Agr) system. Agr-dependent repression of ssl expression is indirect and mediated by the transcription factor repressor of toxins (Rot). Surprisingly, we observed that Rot directly interacts with and activates the ssl promoters. The role of Agr and Rot as regulators of ssl expression was observed across several clinically relevant strains, suggesting that overproduction of immunomodulatory proteins benefits agr-defective strains. In support of this notion, we demonstrate that Ssls contribute to the residual virulence of S. aureus lacking agr in a murine model of systemic infection. Altogether, these results suggest that S. aureus compensates for the inactivation of Agr by producing immunomodulatory exoproteins that could protect the bacterium from host-mediated clearance.
引用
收藏
页码:659 / 675
页数:17
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