The Sbi Protein Contributes to Staphylococcus aureus Inflammatory Response during Systemic Infection

被引:21
|
作者
Daniela Gonzalez, Cintia [1 ]
Ledo, Camila [2 ]
Giai, Constanza [1 ]
Garofalo, Ailin [1 ]
Gomez, Marisa I. [1 ,2 ]
机构
[1] Univ Buenos Aires, Inst Invest Microbiol & Parasitol Med IMPaM, CONICET, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Med, Dept Microbiol Parasitol & Immunol, Buenos Aires, DF, Argentina
来源
PLOS ONE | 2015年 / 10卷 / 06期
关键词
IMMUNE EVASION; BINDING PROTEIN; INTERLEUKIN-6; RECEPTOR; COMPLEMENT; SEPSIS; IGG; EXPRESSION; BLOCKADE; IL-6;
D O I
10.1371/journal.pone.0131879
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Staphylococcus aureus is an important human pathogen that causes infections that may present high morbidity and mortality. Among its many virulence factors protein A (SpA) and Staphylococcal binding immunoglobulin protein (Sbi) bind the Fc portion of IgG interfering with opsonophagocytosis. We have previously demonstrated that SpA interacts with the TNF-alpha receptor (TNFR) 1 through each of the five IgG binding domains and induces the production of pro-inflammatory cytokines and chemokines. The IgG binding domains of Sbi are homologous to those of SpA, which allow us to hypothesize that Sbi might also have a role in the inflammatory response induced by S. aureus. We demonstrate that Sbi is a novel factor that participates in the induction of the inflammatory response during staphylococcal infections via TNFR1 and EGFR mediated signaling as well as downstream MAPKs. The expression of Sbi significantly contributed to IL-6 production and modulated CXCL-1 expression as well as neutrophil recruitment to the site of infection, thus demonstrating for the first time its relevance as a pro-inflammatory staphylococcal antigen in an in vivo model.
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页数:14
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