Diaz J L, Heckels J E
J Gen Microbiol. 1982 Mar;128(3):585-91. doi: 10.1099/00221287-128-3-585.
Antibodies were detected by an enzyme-linked immunosorbent assay (ELISA) in sera from rabbits immunized wtih outer membranes from colonial opacity variants in Neisseria gonorrhoeae P9. ELISA-inhibition experiments with purified antigens revealed approximately equal proportions of antibodies directed against each of the three major surface antigens, lipopolysaccharide, the major outer membrane protein (protein I) and protein II, the variable protein associated with colonial opacity. Inhibition experiments with intact gonococci showed considerable antigenic diversity which could be correlated with differences between the protein II species present. Despite their considerable structural homology, different protein II species from colonial variants of the same strain showed little cross-reactivity with specific anti-protein II sera, thus demonstrating the considerable variation in that part of the antigen which is exposed on the surface of the gonococcus and is closely involved in pathogenic mechanisms.
采用酶联免疫吸附测定(ELISA)检测用淋病奈瑟菌P9的菌落不透明变异株外膜免疫的兔血清中的抗体。用纯化抗原进行的ELISA抑制实验表明,针对三种主要表面抗原(脂多糖、主要外膜蛋白(蛋白I)和蛋白II,即与菌落不透明性相关的可变蛋白)的抗体比例大致相等。用完整淋球菌进行的抑制实验显示出相当大的抗原多样性,这可能与存在的蛋白II种类之间的差异有关。尽管同一菌株的菌落变异株的不同蛋白II种类具有相当大的结构同源性,但它们与特异性抗蛋白II血清几乎没有交叉反应,从而证明了在淋球菌表面暴露且密切参与致病机制的那部分抗原存在相当大的变异。