Schmitz S, Abe C, Moser I, Orskov I, Orskov F, Jann B, Jann K
Infect Immun. 1986 Jan;51(1):54-9. doi: 10.1128/iai.51.1.54-59.1986.
Hybridoma-derived monoclonal antibodies were produced with fimbrial preparations from Escherichia coli 20025 (04:K12:H-) with fimbrial (F) antigens 1C, 13, one related to 12, and one preliminarily termed y and from E. coli 2980 (018ac:K5:H-) with F antigens 1C and 8. Two clones of subclonal hybrid cells were studied which produced monoclonal antibodies (mc-20025-F2b, immunoglobulin G2b [IgG2b]; mc-2980-F2, IgG1) that were reactive with E. coli 20025, 2980, and a number of additional strains which exhibited the F1C antigen. Results of enzyme-linked immunosorbent assay and Western blot analysis indicated that the antibodies had F1C specificity, and competitive enzyme-linked immunosorbent assay with 125I-labeled antibodies showed that they recognized different epitopes on the fimbrial subunit. Neither of the antibodies agglutinated F1C-fimbriated E. coli but bound to the bacteria. There was no binding to E. coli without F1C fimbriae.
利用大肠杆菌20025(04:K12:H-)的菌毛制剂制备杂交瘤衍生的单克隆抗体,该制剂含有菌毛(F)抗原1C、13、一种与12相关的抗原以及一种初步命名为y的抗原;同时利用大肠杆菌2980(018ac:K5:H-)的菌毛制剂制备单克隆抗体,该制剂含有F抗原1C和8。研究了两个亚克隆杂交细胞克隆,它们产生的单克隆抗体(mc-20025-F2b,免疫球蛋白G2b [IgG2b];mc-2980-F2,IgG1)与大肠杆菌20025、2980以及其他一些表达F1C抗原的菌株发生反应。酶联免疫吸附测定和蛋白质印迹分析结果表明,这些抗体具有F1C特异性,用125I标记抗体进行的竞争性酶联免疫吸附测定表明,它们识别菌毛亚基上的不同表位。这两种抗体均未凝集F1C菌毛化的大肠杆菌,但能与细菌结合。对无F1C菌毛的大肠杆菌无结合作用。