Tompkins D C, Blackwell L J, Hatcher V B, Elliott D A, O'Hagan-Sotsky C, Lowy F D
Department of Medicine, State University of New York, Stony Brook 11794.
Infect Immun. 1992 Mar;60(3):965-9. doi: 10.1128/iai.60.3.965-969.1992.
The adherence of Staphylococcus aureus to human endothelial cells is saturable in both dose- and time-dependent assays. Staphylococcal surface components which bound to endothelial cells in vitro were identified by using biotin-labeled, solubilized staphylococcal proteins. Four trypsin-sensitive components with molecular sizes of 30, 55 to 57, 70, and 85 kDa were recognized. These proteins did not label with the glycan detection system. When staphylococci were harvested during the exponential phase of growth, staphylococcal adherence to endothelial cells was significantly increased and increased expression of the S. aureus binding proteins was observed. Preincubation of endothelial cells with protein A did not reduce S. aureus adherence in an in vitro infection assay. Four S. aureus surface components whose expression is growth phase dependent adhere to human endothelial cells in vitro.
在剂量和时间依赖性试验中,金黄色葡萄球菌对人内皮细胞的黏附是可饱和的。通过使用生物素标记的、可溶解的葡萄球菌蛋白,鉴定了体外与内皮细胞结合的葡萄球菌表面成分。识别出了四种分子大小分别为30、55至57、70和85 kDa的对胰蛋白酶敏感的成分。这些蛋白质不能用聚糖检测系统标记。当在生长指数期收获葡萄球菌时,葡萄球菌对内皮细胞的黏附显著增加,并且观察到金黄色葡萄球菌结合蛋白的表达增加。在体外感染试验中,用蛋白A预孵育内皮细胞不会降低金黄色葡萄球菌的黏附。四种表达依赖于生长阶段的金黄色葡萄球菌表面成分在体外与人内皮细胞黏附。