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Immunomagnetic Separation and Coagglutination of Vibrio parahaemolyticus with Anti-Flagellar Protein Monoclonal Antibody

机译:抗纤毛蛋白单克隆抗体的免疫磁分离和凝集性溶血弧菌

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摘要

Mice were immunized by injection of Vibrio parahaemolyticus ATCC 17802 polar flagellin in order to produce monoclonal antibodies (mAbs). mAbs were analyzed by anti-H enzyme-linked immunosorbent assay using V. parahaemolyticus polar flagellar cores. The mAb exhibiting the highest anti-H titer was coated onto Cowan I Staphylococcus aureus cells at a concentration of 75 μg/ml cell suspension and used for slide coagglutination. Of 41 isolates identified genetically as V. parahaemolyticus, 100% coagglutinated with the anti-H mAb within 30 s, and the mAb did not react with 30 isolates identified as Vibrio vulnificus. A strong coagglutination reaction with V. parahaemolyticus ATCC 17802 was still observed when the S. aureus cells were armed with as little as 15 μg of mAb/ml S. aureus cell suspension. At this concentration, the mAb cross-reacted with three other Vibrio species, suggesting that they share an identical H antigen or antigens. The anti-H mAb was then used to optimize an immunomagnetic separation protocol which exhibited from 35% to about 45% binding of 102 to 103 V. parahaemolyticus cells in phosphate-buffered saline. The mAb would be useful for the rapid and selective isolation, concentration, and detection of V. parahaemolyticus cells from environmental sources.
机译:通过注射副溶血性弧菌ATCC 17802极性鞭毛蛋白对小鼠免疫,以产生单克隆抗体(mAb)。使用抗溶血弧菌极性鞭毛核心通过抗H酶联免疫吸附法分析mAb。将具有最高抗H滴度的mAb以75μg/ ml细胞悬液的浓度包被在Cowan I金黄色葡萄球菌细胞上,并用于载玻片凝集。从基因上鉴定为副溶血性弧菌的41个分离株中,有100%在30 s内与抗H mAb凝集,并且mAb不与30个被鉴定为创伤弧菌的分离株反应。当金黄色葡萄球菌细胞用低至15μgmAb / ml金黄色葡萄球菌细胞悬液武装时,仍观察到与副溶血性弧菌ATCC 17802的​​强烈凝集反应。在此浓度下,mAb与其他三个弧菌属物种发生交叉反应,表明它们共享相同的一种或多种H抗原。然后使用抗H mAb优化免疫磁分离方案,该方案在磷酸盐中显示10 2 与10 3 溶血弧菌细胞的35%到大约45%的结合缓冲盐水。 mAb可用于从环境来源快速选择性地分离,浓缩和检测溶血性弧菌细胞。

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