The FbaB-type fibronectin-binding protein of Streptococcus pyogenes promotes specific invasion into endothelial cells

被引:48
作者
Amelung, Silva [1 ]
Nerlich, Andreas [1 ]
Rohde, Manfred [1 ]
Spellerberg, Barbara [2 ]
Cole, Jason N. [3 ,4 ]
Nizet, Victor [3 ,4 ]
Chhatwal, Gursharan S. [1 ]
Talay, Susanne R. [1 ]
机构
[1] Helmholtz Ctr Infect Res, Dept Med Microbiol, D-38124 Braunschweig, Germany
[2] Univ Hosp Ulm, Dept Med Microbiol & Hyg, Ulm, Germany
[3] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
基金
英国医学研究理事会;
关键词
GROUP-A STREPTOCOCCI; SHOCK-LIKE SYNDROME; EPITHELIAL-CELLS; LIVING CELLS; DOMAIN; SFBI; INTERNALIZATION; INFECTIONS; ACTIVATION; PHAGOSOME;
D O I
10.1111/j.1462-5822.2011.01610.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Invasive serotype M3 Streptococcus pyogenes are among the most frequently isolated organisms from patients suffering from invasive streptococcal disease and have the potential to invade primary human endothelial cells (EC) via a rapid and efficient mechanism. FbaB protein, the fibronectin-binding protein expressed by M3 S. pyogenes, was herein identified as a potent invasin for EC. By combining heterologous gene expression with allelic replacement, we demonstrate that FbaB is essential and sufficient to trigger EC invasion via a Rac1-dependent phagocytosis-like uptake. FbaB-mediated uptake follows the classical endocytic pathway with lysosomal destination. FbaB is demonstrated to be a streptococcal invasin exhibiting EC tropism. FbaB thus initiates a process that may contribute to the deep tissue tropism and spread of invasive S. pyogenes isolates into the vascular EC lining.
引用
收藏
页码:1200 / 1211
页数:12
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