Division of Infection Medicine, Department of Clinical Sciences, Biomedical Center, Lund University, Lund, Sweden.
J Innate Immun. 2010;2(2):160-6. doi: 10.1159/000232587. Epub 2009 Aug 1.
Bacterial engagement of specific host tissue structures can be a means of targeting a pathogen to a particular niche, establishing persistent infections and inducing invasion. In this context, primary adhesion is often the first crucial colonization step allowing pathogens to withstand the mechanical clearing mechanisms of the host. As a consequence, bacteria have evolved adhesins with the capacity to mediate interaction between microorganism and host. Here we describe collagen VI as a novel target for adherence of Streptococcus pyogenes and Streptococcus pneumoniae. In upper and lower airways this collagen was distributed in the lamina propria underneath the epithelial basement membrane. Both pathogens exhibited strong affinity to collagen VI as shown by light and electron microscopy in combination with immunodetection and in vitro binding assays. For S. pyogenes this interaction was mediated by M1 protein. The presented data provide evidence for a previously unrecognized role for collagen VI in host-pathogen interplay during respiratory tract infection.
细菌与特定宿主组织结构的结合可以作为将病原体靶向特定小生境的一种手段,从而建立持续性感染并诱导入侵。在这种情况下,最初的黏附通常是第一个关键的定植步骤,使病原体能够抵抗宿主的机械清除机制。因此,细菌已经进化出具有介导微生物与宿主之间相互作用能力的黏附素。在这里,我们将胶原 VI 描述为酿脓链球菌和肺炎链球菌黏附的一个新靶点。在上呼吸道和下呼吸道中,这种胶原蛋白分布在位于上皮基底膜下的固有层中。通过光镜和电镜结合免疫检测和体外结合实验,两种病原体都表现出对胶原 VI 的强烈亲和力。对于酿脓链球菌,这种相互作用是由 M1 蛋白介导的。所呈现的数据为呼吸道感染过程中胶原 VI 在宿主-病原体相互作用中发挥的先前未被认识到的作用提供了证据。