Wenman W M, Meuser R U
J Bacteriol. 1986 Feb;165(2):602-7. doi: 10.1128/jb.165.2.602-607.1986.
Chlamydia trachomatis proteins were electrophoresed and then transferred to nitrocellulose paper to detect chlamydial proteins which bind to eucaryotic cell membranes. Resolved polypeptides of C. trachomatis serovars J and L2 were reacted with iodinated HeLa cell membranes and autoradiographed. Infectious elementary bodies of both serovars possess 31,000- and 18,000-dalton proteins which bind to HeLa cells. In contrast, noninfectious reticulate bodies do not possess eucaryotic cell-binding proteins. Both proteins are antigenic when reacted with hyperimmune rabbit antisera in immunoblots and antisera raised against the 31,000- and 18,000-dalton proteins are inhibitory to chlamydia-host cell association. In addition, these antisera exhibit neutralizing activity. Our data suggest that these putative chlamydial adhesins play a key role in the early steps of chlamydia-host cell interaction and that antibody directed against them may be protective.
沙眼衣原体蛋白经电泳后转移至硝酸纤维素纸上,以检测与真核细胞膜结合的衣原体蛋白。将沙眼衣原体血清型J和L2的分离多肽与碘化的HeLa细胞膜反应并进行放射自显影。两种血清型的感染性原体均具有与HeLa细胞结合的31,000道尔顿和18,000道尔顿的蛋白。相比之下,非感染性网状体不具有真核细胞结合蛋白。在免疫印迹中,当这两种蛋白与超免疫兔抗血清反应时均具有抗原性,并且针对31,000道尔顿和18,000道尔顿蛋白产生的抗血清可抑制衣原体与宿主细胞的结合。此外,这些抗血清具有中和活性。我们的数据表明,这些假定的衣原体粘附素在衣原体与宿主细胞相互作用的早期步骤中起关键作用,并且针对它们的抗体可能具有保护作用。