Quantification of staphylococcal-collagen binding interactions in whole blood by use of a confocal microscopy shear-adhesion assay.

Quantification of staphylococcal-collagen binding interactions in whole blood by use of a confocal microscopy shear-adhesion assay.
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使用共聚焦显微镜剪切粘附测定对全血中葡萄球菌-胶原蛋白结合相互作用进行定量。

DOI:
10.1086/375826
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发表时间:
2003
期刊:
The Journal of infectious diseases.
影响因子:
--
通讯作者:
Ross,JuliaM
Ross,JuliaM
中科院分区:
--
文献类型:
--
作者:
Mascari,LisaM;Ross,JuliaM

文献摘要

被引文献

相似文献

在血源性葡萄球菌感染中,细菌和血小板经常联合收割机,在暴露胶原的内皮下形成血栓。在这个过程中,胶原蛋白作为金黄色葡萄球菌的潜在结合表面。然而,S.金-胶原结合相互作用在感染血栓形成中的作用尚不确定。我们量化了S.在确定的生理相关流体剪切条件下,在全血悬浮液中,金黄色与胶原的粘附。金黄色葡萄球菌-胶原蛋白结合相互作用,由S.金黄色胶原粘附素(CNA)和蛋白A-血管性血友病因子(vWf),使用突变株和抗体阻断技术进行了评估。使用共聚焦激光显微镜测量粘附细菌的位置(在胶原蛋白表面处或在血小板聚集体中的表面上方)。结果表明在生理剪切条件下显著的CNA-胶原相互作用和蛋白A-vWf-胶原结合相互作用。我们的结论是,胶原蛋白结合的相互作用是重要的感染血栓的发展。
In bloodborne staphylococcal infections, bacteria and platelets often combine, forming thrombi on the subendothelium, where collagen is exposed. In this process, the collagen serves as a potential binding surface forStaphylococcus aureus. However, the extent and importance ofS. aureus-collagen binding interactions in the development of infected thrombi is uncertain. We quantifiedS. aureusadhesion to collagen in a whole-blood suspension under defined physiologically relevant fluid shear conditions.S. aureus-collagen binding interactions, mediated by both theS. aureuscollagen adhesin (CNA) and protein A-von Willebrand factor (vWf), were evaluated using mutant strains and antibody-blocking techniques. The position of adherent bacteria (at the collagen surface or above the surface in the platelet aggregate) was measured using confocal laser microscopy. Results demonstrated significant CNA-collagen interactions and protein A-vWf-collagen binding interactions under physiological shear conditions. We conclude that collagen binding interactions are important in the development of infected thrombi.