首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Detection and characterization of the coli surface antigen 6 of enterotoxigenic Escherichia coli strains by using monoclonal antibodies.
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Detection and characterization of the coli surface antigen 6 of enterotoxigenic Escherichia coli strains by using monoclonal antibodies.

机译:使用单克隆抗体检测和鉴定产肠毒素的大肠杆菌菌株的大肠杆菌表面抗原6。

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摘要

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.
机译:我们首次描述了针对产肠毒素性大肠杆菌(ETEC)的大肠杆菌表面抗原6(CS6)的单克隆抗体(MAb)的生产及其在CS6的表征和诊断中的用途。通过用纯化的含CS6或CS6的细菌提取物免疫小鼠,可产生两种单克隆抗体,即单克隆抗体CS6-20:11:9和CS6-2A:14。通过酶联免疫吸附测定(ELISA),免疫印迹和免疫电子显微镜法证明了MAb的特异性,这表明MAb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定居因子。通过使用细菌重组体,即具有完整CS6操纵子或其部分的菌株,发现两个MAb对CS6的两个结构亚基之一的CssB具有特异性。尽管单克隆抗体特异性结合表达CS6的细菌的整个表面,但无法鉴定CS6的结构。在抑制ELISA和斑点印迹测试中评估了单克隆抗体对CS6检测的有用性。分析了九十二个具有已知定殖因子的ETEC菌株,并通过MAb CS6-2A:14的任一种测定法鉴定了所有CS6-阳性菌株,而MAb CS6-20:11:9未能鉴定出两个CS6-阳性菌株。在任何情况下,任何一个单克隆抗体均未鉴定出任何CS6阴性菌株。用对CS6的另一个结构亚基即CssA有特异性的基因探针对48株菌株进行的平行分析和基于MAb的测定得出了相同的结果,表明两个亚基同时存在。

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