Datta S, Janes M E, Simonson J G
Department of Food Science, Louisiana State University AgCenter, Baton Rouge, LA 70803, USA.
Clin Vaccine Immunol. 2008 Oct;15(10):1541-6. doi: 10.1128/CVI.00141-08. Epub 2008 Aug 27.
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 microg/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 microg 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 10(2) to 10(3) 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.
通过注射副溶血性弧菌ATCC 17802极鞭毛蛋白对小鼠进行免疫,以产生单克隆抗体(mAb)。使用副溶血性弧菌极鞭毛核心通过抗H酶联免疫吸附测定法分析单克隆抗体。将表现出最高抗H效价的单克隆抗体以75微克/毫升细胞悬液的浓度包被在考恩I型金黄色葡萄球菌细胞上,并用于玻片凝集试验。在41株经基因鉴定为副溶血性弧菌的分离株中,100%在30秒内与抗H单克隆抗体发生凝集反应,且该单克隆抗体与30株鉴定为创伤弧菌的分离株不发生反应。当金黄色葡萄球菌细胞仅用15微克/毫升金黄色葡萄球菌细胞悬液的单克隆抗体武装时,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,该单克隆抗体与其他三种弧菌发生交叉反应,表明它们共享一种或多种相同的H抗原。然后使用抗H单克隆抗体优化免疫磁分离方案,该方案在磷酸盐缓冲盐水中对10²至10³个副溶血性弧菌细胞的结合率为35%至约45%。该单克隆抗体可用于从环境来源中快速、选择性地分离、浓缩和检测副溶血性弧菌细胞。