Characterization of monoclonal antibodies against Erwinia carotovora subsp. atroseptica serogroup I: specificity and epitope analysis.

The Journal of applied bacteriology Pub Date : 1995-04-01
L J Hyman, A Wallace, M M Lopez, M Cambra, M T Gorris, M C Pérombelon
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Abstract

The characteristics of two monoclonal antibodies (Mabs), A23/1221.59.44.d.3 (1221) and A23/1239.36.64.e.2 (1239), against Erwinia carotovora subsp. atroseptica serogroup I produced in this study were compared with those of two other independently obtained Mabs, 4G4 in Spain and 4F6 in Canada, using different strains as immunogen and different screening procedures. The reaction pattern of Mabs 1221 and 1239 determined by indirect ELISA on over 200 bacterial strains including five E.c. atroseptica and 36 E.c. carotovora serogroups, seven Erw. chrysanthemi biovars, 23 other plant bacterial pathogens and 33 saprophytic bacteria from potato was similar to that of 4G4. Specificity for E.c. atroseptica serogroup I was improved, especially when skimmed milk (Marvel) was used instead of bovine serum albumin as blocking agent. Mabs 1221, 1239 and 4G4 reacted positively with all 22 E.c. atroseptica serogroup I, the dominant E.c. atroseptica serogroup on potato, strains tested and only with two out of five E.c. atroseptica serogroup XXII strains, one E.c. carotovora serogroup XXI strain and one strain of a saprophytic bacterium, Comamonas sp. Essentially similar results were obtained when examined by immunofluorescence. Characterization of the four Mabs showed that they were IgG3 and SDS-PAGE/immunoblot results suggested that they were probably against the O-side chain of bacterial cell wall lipopolysaccharides. In competition ELISA between biotin-labelled and unlabelled Mabs, the competition pattern of the four Mabs was similar.(ABSTRACT TRUNCATED AT 250 WORDS)

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抗胡萝卜Erwinia carotovora亚种单克隆抗体的鉴定。atroseptica血清I组:特异性和表位分析。
两种单克隆抗体(mab), A23/1221.59.44.d.3(1221)和A23/1239.36.64.e.2(1239),对Erwinia carotovora subsp。本研究生产的atroseptica血清I组与另外两种独立获得的mab(西班牙的4G4和加拿大的4F6)进行比较,采用不同的菌株作为免疫原,采用不同的筛选程序。采用间接ELISA法测定了单抗1221和1239对200多种细菌的反应规律,其中包括5个atroseptica菌群和36个carotovora菌群,7个Erw。菊花生物变异、其他植物病原菌23种、马铃薯腐生菌33种与4G4相似。特别是当用脱脂牛奶代替牛血清白蛋白作为阻断剂时,对atroseptica血清I组的特异性得到了提高。单克隆抗体1221、1239和4G4与22个萎败性大肠杆菌血清群ⅰ(马铃薯上占优势的萎败性大肠杆菌血清群)均有阳性反应,仅与5个萎败性大肠杆菌血清群XXII中的2个、1个胡萝卜性大肠杆菌血清群XXI菌株和1个腐生菌Comamonas sp的菌株有阳性反应。免疫荧光检测结果基本相似。鉴定结果表明,这4个单抗均为IgG3, SDS-PAGE/免疫印迹结果表明,它们可能是针对细菌细胞壁脂多糖的o侧链。在生物素标记单抗与未标记单抗的竞争ELISA中,4种单抗的竞争模式相似。(摘要删节250字)
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