Gray-Owen Scott D
Department of Medical Genetics and Microbiology, University of Toronto, Toronto, Ontario, Canada.
Scand J Infect Dis. 2003;35(9):614-8. doi: 10.1080/00365540310016042.
The pathogenic Neisseria sp. encode a family of phase-variable and antigenically distinct Opa proteins that allow bacterial attachment to virtually every cell type encountered during infection. Some Opa variants bind cell surface-expressed heparan sulfate proteoglycans, including members of the syndecan family of receptors, and extracellular matrix proteins such as fibronectin and vitronectin. Other variants bind members of the carcinoembryonic antigen family of cellular adhesion molecules. Depending on the Opa variant(s) expressed, these receptor interactions can allow neisserial entry and transcellular transcytosis across polarized epithelial cell monolayers, entry into endothelial cells, suppression of lymphocyte function and/or bacterial engulfment and killing by neutrophils. Recent advances in our understanding of how these Opa protein-mediated interactions influence the host cellular response are discussed in the context of their impact on various stages of neisserial infection.
致病性奈瑟菌属编码一族相位可变且抗原性不同的Opa蛋白,这些蛋白使细菌能够附着于感染过程中几乎遇到的每一种细胞类型。一些Opa变体结合细胞表面表达的硫酸乙酰肝素蛋白聚糖,包括多配体蛋白聚糖受体家族的成员,以及细胞外基质蛋白,如纤连蛋白和玻连蛋白。其他变体结合细胞粘附分子癌胚抗原家族的成员。根据所表达的Opa变体,这些受体相互作用可使奈瑟菌进入并跨极化上皮细胞单层进行跨细胞转运,进入内皮细胞,抑制淋巴细胞功能和/或被中性粒细胞吞噬和杀伤。本文在这些Opa蛋白介导的相互作用对奈瑟菌感染各个阶段的影响的背景下,讨论了我们对其如何影响宿主细胞反应的最新认识进展。