Institut für Medizinische Mikrobiologie und Krankenhaushygiene, Klinikum der Goethe Universität, Paul Ehrlich Str. 40, D-60596 Frankfurt am Main, Germany.
Infect Immun. 2011 Jul;79(7):2544-53. doi: 10.1128/IAI.01309-10. Epub 2011 May 2.
Trimeric autotransporter adhesins (TAAs) are important virulence factors of Gram-negative bacteria responsible for adherence to extracellular matrix (ECM) and host cells. Here, we analyzed three different TAAs (Bartonella adhesin A [BadA] of Bartonella henselae, variably expressed outer membrane proteins [Vomps] of Bartonella quintana, and Yersinia adhesin A [YadA] of Yersinia enterocolitica) for mediating bacterial adherence to ECM and endothelial cells. Using static (cell culture vials) and dynamic (capillary flow chambers) experimental settings, adherence of wild-type bacteria and of the respective TAA-negative strains was analyzed. Under static conditions, ECM adherence of B. henselae, B. quintana, and Y. enterocolitica was strongly dependent on the expression of their particular TAAs. YadA of Y. enterocolitica did not mediate bacterial binding to plasma or cellular fibronectin under either static or dynamic conditions. TAA-dependent host cell adherence appeared more significant under dynamic conditions although the total number of bound bacteria was diminished compared to the number under static conditions. Dynamic models expand the methodology to perform bacterial adherence experiments under more realistic, bloodstream-like conditions and allow dissection of the biological role of TAAs in ECM and host cell adherence under static and dynamic conditions.
三聚体自转运黏附素(TAAs)是革兰氏阴性菌的重要毒力因子,负责与细胞外基质(ECM)和宿主细胞黏附。在这里,我们分析了三种不同的 TAAs(亨氏巴尔通体的 Bartonella 黏附素 A [BadA]、巴尔通体 quintana 的可变表达外膜蛋白 [Vomps] 和小肠结肠炎耶尔森菌的 Yersinia 黏附素 A [YadA])介导细菌与 ECM 和内皮细胞黏附的能力。使用静态(细胞培养小瓶)和动态(毛细管流动室)实验设置,分析了野生型细菌和相应 TAA 阴性菌株的黏附情况。在静态条件下,B. henselae、B. quintana 和 Y. enterocolitica 的 ECM 黏附强烈依赖于其特定 TAAs 的表达。Y. enterocolitica 的 YadA 既不能介导细菌与血浆或细胞纤维连接蛋白在静态或动态条件下的结合。尽管与静态条件下的细菌数量相比,动态条件下结合的细菌总数减少,但 TAA 依赖性宿主细胞黏附似乎更为显著。动态模型扩展了在更接近真实血流条件下进行细菌黏附实验的方法,并允许在静态和动态条件下剖析 TAAs 在 ECM 和宿主细胞黏附中的生物学作用。