Dickinson R B, Nagel J A, McDevitt D, Foster T J, Proctor R A, Cooper S L
Department of Chemical Engineering, University of Florida, Gainesville 32611, USA.
Infect Immun. 1995 Aug;63(8):3143-50. doi: 10.1128/iai.63.8.3143-3150.1995.
The contributions of clumping factor and coagulase in mediating Staphylococcus aureus adhesion to surface-adsorbed fibrinogen have been quantified by using a new methodology and analysis. The attachment or detachment kinetics of bacteria were directly observed in a radial flow chamber with a well-defined laminar flow field and a spatially varying shear rate and were quantified by recursively scanning the chamber surface and counting cells via automated video microscopy and image analysis with a motorized stage and focus control. Intrinsic rate constants for attachment or detachment were estimated as functions of shear rate for the wild-type Newman strain of S. aureus and for mutants lacking clumping factor, coagulase, or both proteins on surfaces coated with plasma, fibrinogen, or albumin. Clumping factor, but not coagulase, increased the probability of attachment and decreased the probability of detachment of S. aureus on plasma-coated surfaces; however, both clumping factor and, to a lesser extent, coagulase increased the probability of attachment on the purified-fibrinogen-coated surface. All mutants were resistant to detachment on the purified-fibrinogen-coated surface, suggesting the possibility of an additional adhesion mechanism which was independent of coagulase or clumping factor and effective only for fully attached cells. Together, these results suggest that the presence of clumping factor plays the primary role in enhancing adhesion to surfaces with adsorbed fibrinogen, not only by enhancing the probability of cell attachment but also by increasing the strength of the resulting adhesion.
通过使用一种新的方法和分析手段,已对聚集因子和凝固酶在介导金黄色葡萄球菌黏附于表面吸附的纤维蛋白原过程中的作用进行了定量。在具有明确层流场和空间变化剪切速率的径向流动腔室中直接观察细菌的附着或脱离动力学,并通过自动视频显微镜和图像分析,利用电动载物台和聚焦控制对腔室表面进行递归扫描并计数细胞,从而对其进行定量。对于金黄色葡萄球菌的野生型纽曼菌株以及在涂有血浆、纤维蛋白原或白蛋白的表面上缺乏聚集因子、凝固酶或这两种蛋白质的突变体,估计了附着或脱离的固有速率常数与剪切速率的函数关系。聚集因子而非凝固酶增加了金黄色葡萄球菌在血浆包被表面上的附着概率并降低了脱离概率;然而,聚集因子以及在较小程度上凝固酶均增加了在纯化纤维蛋白原包被表面上的附着概率。所有突变体在纯化纤维蛋白原包被表面上均抗脱离,这表明可能存在一种独立于凝固酶或聚集因子且仅对完全附着细胞有效的额外黏附机制。总之,这些结果表明聚集因子的存在在增强对吸附有纤维蛋白原的表面的黏附中起主要作用,这不仅通过提高细胞附着概率,还通过增加所形成黏附的强度来实现。