Sugasawara R J, Cannon J G, Black W J, Nachamkin I, Sweet R L, Brooks G F
Infect Immun. 1983 Dec;42(3):980-5. doi: 10.1128/iai.42.3.980-985.1983.
This study showed that a protein II (PII) of Neisseria gonorrhoeae FA1090 appeared to act as a mediator of attachment to HeLa cells. Two colony variants of FA1090 were selected. Both gonococcal variants were nonpiliated, but one contained a PII and the other did not. A monoclonal antibody (1090-10.1), which was directed against the PII, inhibited the apparent PII-mediated attachment to HeLa cells. Antibodies produced from clone 1035-4, which had no PII specificity, did not inhibit the attachment and were used as controls. Inhibition of gonococcal attachment by the 1090-10.1 monoclonal antibodies was demonstrated by fluorescent microscopy analysis. Monoclonal antibody 1090-10.1 appeared to cause agglutination of the PII-containing organism. To block the clumping caused by the PII-specific monoclonal antibodies, Fab fragments of goat anti-mouse IgG were incubated with gonococci and the 1090-10.1 monoclonal antibodies. The results showed that the goat anti-mouse IgG Fab fragments partially blocked the agglutination caused by the PII-specific monoclonal antibody. The effect of the 1090-10.1 antibodies on attachment was also determined by monitoring the HeLa cells with attached iodinated gonococci. The monoclonal antibody appeared to inhibit the PII-mediated attachment.
这项研究表明,淋病奈瑟菌FA1090的蛋白质II(PII)似乎充当了与HeLa细胞附着的介质。选择了FA1090的两个菌落变体。这两种淋球菌变体均无菌毛,但一种含有PII,另一种不含。一种针对PII的单克隆抗体(1090-10.1)抑制了明显的PII介导的与HeLa细胞的附着。由克隆1035-4产生的无PII特异性的抗体不抑制附着,并用作对照。通过荧光显微镜分析证实了1090-10.1单克隆抗体对淋球菌附着的抑制作用。单克隆抗体1090-10.1似乎导致含PII的生物体发生凝集。为了阻断由PII特异性单克隆抗体引起的凝集,将山羊抗小鼠IgG的Fab片段与淋球菌和1090-10.1单克隆抗体一起孵育。结果表明,山羊抗小鼠IgG Fab片段部分阻断了由PII特异性单克隆抗体引起的凝集。还通过监测附着有碘化淋球菌的HeLa细胞来确定1090-10.1抗体对附着的影响。该单克隆抗体似乎抑制了PII介导的附着。