Cloeckaert A, Zygmunt M S, Dubray G, Limet J N
Unit of Experimental Medicine, Catholic University of Louvain, Brussels, Belgium.
J Gen Microbiol. 1993 Jul;139(7):1551-6. doi: 10.1099/00221287-139-7-1551.
Twenty-two monoclonal antibodies (mAbs) specific for smooth lipopolysaccharide (S-LPS) were generated by fusion of spleen cells from mice infected with the rough Brucella melitensis strain B115 with the NSO myeloma. According to reactivity in enzyme-linked immunosorbent assay (ELISA) with O-polysaccharide (O-PS) and absence of reactivity with rough lipopolysaccharide (R-LPS), it was postulated that these mAbs recognized epitopes present on the O-PS. Most of the mAbs reacted equally well in ELISA and immunoblotting with S-LPS types of Brucella A and M dominant strains and were designated as specific for common (C) epitopes. Three mAbs were highly specific for M dominant S-LPS. All these mAbs, in contrast to a mAb specific for the A epitope, showed little or no cross-reactivity with Yersinia enterocolitica O:9 S-LPS. S-LPS of B. melitensis B115 was extracted and analysed by immunoblotting and ELISA with mAbs specific for A, M and C epitopes. Reactivity of the mAbs with this S-LPS was compared to reactivity with S-LPS of A and M dominant smooth Brucella strains. The results suggest that S-LPS of B. melitensis B115 bears mainly C epitopes and a few M epitopes. The very weak reactivity of this S-LPS with the mAb specific for the A epitope and the fact that the mAbs specific for C and M epitopes showed little or no cross-reactivity with Y. enterocolitica O:9 S-LPS suggest that O-PS from this rough strain could be used to distinguish Y. enterocolitica O:9 infection from Brucella infection.(ABSTRACT TRUNCATED AT 250 WORDS)
通过将感染粗糙型布鲁氏菌羊种菌株B115的小鼠脾细胞与NSO骨髓瘤细胞融合,产生了22种针对光滑脂多糖(S-LPS)的单克隆抗体(mAb)。根据酶联免疫吸附测定(ELISA)中与O-多糖(O-PS)的反应性以及与粗糙脂多糖(R-LPS)无反应性,推测这些mAb识别存在于O-PS上的表位。大多数mAb在ELISA和免疫印迹中与布鲁氏菌A和M优势菌株的S-LPS类型反应良好,被指定为对共同(C)表位具有特异性。三种mAb对M优势S-LPS具有高度特异性。与针对A表位的mAb相比,所有这些mAb与小肠结肠炎耶尔森菌O:9 S-LPS几乎没有交叉反应性。提取布鲁氏菌羊种B115的S-LPS,并通过免疫印迹和ELISA用针对A、M和C表位的mAb进行分析。将这些mAb与该S-LPS的反应性与与A和M优势光滑布鲁氏菌菌株的S-LPS的反应性进行比较。结果表明,布鲁氏菌羊种B115的S-LPS主要带有C表位和一些M表位。该S-LPS与针对A表位的mAb反应非常弱,以及针对C和M表位的mAb与小肠结肠炎耶尔森菌O:9 S-LPS几乎没有交叉反应性这一事实表明,来自该粗糙菌株的O-PS可用于区分小肠结肠炎耶尔森菌O:9感染与布鲁氏菌感染。(摘要截断于250字)