Mascari L, Ross J M
Department of Chemical and Biochemical Engineering, University of Maryland Baltimore County, Baltimore 21250, USA.
Ann Biomed Eng. 2001 Nov;29(11):956-62. doi: 10.1114/1.1415527.
Dynamic bacterial adhesion has recently gained significant attention due to its role in the initiation of infectious diseases. Staphylococcus aureus binding to collagen has been shown to be an important event in the pathogenesis of infection. Staphylococcal strains have exhibited wide variability in their level of collagen binding, which may be a result of the collagen receptor expression level. In this study, the dynamic adhesion to collagen for several S. aureus strains was quantified at physiological wall shear rates in a parallel-plate flow chamber. In addition, the collagen receptor density was quantified for each strain. An existing theoretical framework was used to analyze the dependence of adhesion on receptor density. Intrinsic kinetic adhesion parameters were determined and demonstrated to be strong functions of receptor density for all strains. These results suggest that staphylococcal adhesion to collagen is heavily dependent on the receptor density. Using this analytical approach it is possible to predict the dynamic adhesion of S. aureus to collagen in vitro by only measuring the collagen receptor density.
由于动态细菌粘附在传染病的引发中所起的作用,它最近受到了广泛关注。金黄色葡萄球菌与胶原蛋白的结合已被证明是感染发病机制中的一个重要事件。葡萄球菌菌株在胶原蛋白结合水平上表现出很大的变异性,这可能是胶原蛋白受体表达水平的结果。在本研究中,在平行板流动腔中,以生理壁面剪切速率对几种金黄色葡萄球菌菌株与胶原蛋白的动态粘附进行了定量。此外,还对每个菌株的胶原蛋白受体密度进行了定量。使用现有的理论框架来分析粘附对受体密度的依赖性。确定了内在动力学粘附参数,并证明其是所有菌株受体密度的强函数。这些结果表明,葡萄球菌对胶原蛋白的粘附严重依赖于受体密度。使用这种分析方法,仅通过测量胶原蛋白受体密度就有可能预测金黄色葡萄球菌在体外与胶原蛋白的动态粘附。