Helander A, Grewal H M, Gaastra W, Svennerholm A M
Department of Medical Microbiology and Immunology, Göteborg University, Sweden.
J Clin Microbiol. 1997 Apr;35(4):867-72. doi: 10.1128/jcm.35.4.867-872.1997.
We describe, for the first time, the production of monoclonal antibodies (MAbs) against coli surface antigen 6 (CS6) of enterotoxigenic Escherichia coli (ETEC) and their use for characterization and diagnosis of CS6. Two MAbs, MAbs CS6-20:11:9 and CS6-2A:14, were produced by immunizing mice with purified CS6 or CS6-containing bacterial extracts. The MAb specificity was demonstrated by enzyme-linked immunosorbent assay (ELISA), immunoblotting, and immunoelectron microscopy, which showed that the MAbs bound to CS6-expressing bacteria as well as to purified CS6 and CS6 structural subunits but not to CS6-negative bacteria or other purified ETEC colonization factors. By using bacterial recombinants, i.e., strains with a complete CS6 operon or parts thereof, it was found that both MAbs were specific for CssB, one of the two structural subunits of CS6. Although the MAbs bound specifically to the entire surface of CS6-expressing bacteria, no structure of CS6 could be identified. The usefulness of the MAbs for the detection of CS6 was evaluated in an inhibition ELISA and in a dot blot test. Ninety-two ETEC strains with known colonization factors were analyzed, and all CS6-positive strains were identified by either assay with MAb CS6-2A:14, whereas MAb CS6-20:11:9 failed to identify two CS6-positive strains; in no instance was any CS6-negative strain identified by either of the MAbs. Parallel analyses of 48 strains with a gene probe specific for the other structural subunit of CS6, i.e., CssA, and the MAb-based assays gave identical results, suggesting the simultaneous presence of both subunits.
我们首次描述了抗产肠毒素大肠杆菌(ETEC)菌毛表面抗原6(CS6)单克隆抗体(MAb)的制备及其在CS6鉴定和诊断中的应用。通过用纯化的CS6或含CS6的细菌提取物免疫小鼠,制备了两种单克隆抗体,即单克隆抗体CS6 - 20:11:9和CS6 - 2A:14。酶联免疫吸附测定(ELISA)、免疫印迹和免疫电子显微镜证实了单克隆抗体的特异性,结果表明这些单克隆抗体与表达CS6的细菌以及纯化的CS6和CS6结构亚基结合,但不与CS6阴性细菌或其他纯化的ETEC定植因子结合。利用细菌重组体,即具有完整CS6操纵子或其部分片段的菌株,发现这两种单克隆抗体均对CS6的两个结构亚基之一CssB具有特异性。尽管单克隆抗体特异性结合表达CS6细菌的整个表面,但未鉴定出CS6的结构。通过抑制ELISA和斑点印迹试验评估了单克隆抗体在检测CS6中的实用性。分析了92株已知定植因子的ETEC菌株,所有CS6阳性菌株均通过单克隆抗体CS6 - 2A:14检测到,而单克隆抗体CS6 - 20:11:9未能鉴定出两株CS6阳性菌株;两种单克隆抗体均未鉴定出任何CS6阴性菌株。用针对CS6另一个结构亚基即CssA的基因探针与基于单克隆抗体的检测方法对48株菌株进行平行分析,结果相同,表明两个亚基同时存在。