Kupsch E M, Knepper B, Kuroki T, Heuer I, Meyer T F
Max-Planck-Institut für Biologie, Abteilung Infektionsbiologie, Tübingen, Germany.
EMBO J. 1993 Feb;12(2):641-50. doi: 10.1002/j.1460-2075.1993.tb05697.x.
Opacity proteins (Opa) of Neisseria gonorrhoeae, a family of variant outer membrane proteins implicated in pathogenesis, are subject to phase variation. In strain MS11, 11 different opa gene alleles have been identified, the expression of which can be turned on and off independently. Using a reverse genetic approach, we demonstrate that a single Opa protein variant of strain MS11, Opa50, enables gonococci to invade epithelial cells. The remaining variant Opa proteins show no, or very little, specificity for epithelial cells but instead confer interaction with human polymorphonuclear neutrophils (PMNs). Thus, depending on the opa allele expressed, gonococci are capable of invading epithelial cells or of interacting with human leukocytes. The respective properties of Opa proteins are maintained independent of the gonococcal strain; thus, the specificity for epithelial cells or leukocytes is intrinsic to Opa proteins. Significant homology exists in the surface exposed variable regions of two invasion supporting Opa proteins from independent strains. Efficient epithelial cell invasion is favoured by high level Opa production, however, a 10-fold reduction still allows significant invasion by gonococci. In contrast, recombinant Escherichia coli expressing Opa proteins adhered or invaded poorly under similar experimental conditions, thus indicating that additional factors besides Opa are required in the Opa-mediated interaction with human cells.
淋病奈瑟菌的不透明蛋白(Opa)是一类与发病机制有关的可变外膜蛋白家族,会发生相变。在MS11菌株中,已鉴定出11种不同的opa基因等位基因,其表达可独立开启和关闭。通过反向遗传学方法,我们证明MS11菌株的单个Opa蛋白变体Opa50能使淋球菌侵入上皮细胞。其余的变体Opa蛋白对上皮细胞无特异性或特异性极低,而是与人类多形核中性粒细胞(PMN)相互作用。因此,根据所表达的opa等位基因,淋球菌能够侵入上皮细胞或与人类白细胞相互作用。Opa蛋白的各自特性与淋球菌菌株无关;因此,对上皮细胞或白细胞的特异性是Opa蛋白固有的。来自独立菌株的两种支持侵袭的Opa蛋白在表面暴露的可变区域存在显著同源性。高水平的Opa产生有利于上皮细胞的有效侵袭,然而,减少10倍仍能使淋球菌进行显著侵袭。相比之下,在类似实验条件下,表达Opa蛋白的重组大肠杆菌粘附或侵袭能力较差,因此表明在Opa介导的与人类细胞相互作用中,除Opa外还需要其他因素。