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首页> 外文期刊>International Journal of Food Microbiology >Development of monoclonal antibody based sandwich ELISA for the rapid detection of pathogenic Vibrio parahaemolyticus in seafood
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Development of monoclonal antibody based sandwich ELISA for the rapid detection of pathogenic Vibrio parahaemolyticus in seafood

机译:快速检测海鲜中致病性副溶血性弧菌的基于单克隆抗体的夹心ELISA的开发

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摘要

Thermostable direct hemolysin (TDH) and TDH-related hemolysin (TRH) are considered important virulence factors of Vibrio parahaemolyticus and strains producing either of these or both are considered pathogenic. In this study, we generated monoclonal antibodies (mAbs) against purified TRH recombinant protein of pathogenic V. parahaemolyticus. Sandwich enzyme-linked immunosorbent assays (ELISA) using the hybridoma clone 4B10 showed higher sensitivity of detection compared to other clones. Using mAb 4B10 based sandwich ELISA, we could detect pathogenic V. parahaemolyticus in 41.18% (14 out of 34) of the seafood samples analyzed. PCR targeting the toxR gene showed the presence of V. parahaemolyticus in 64.7% (22 out of 34) seafood samples. Further, PCR targeting the virulence genes showed that 6 seafood samples harboured the tdh gene while 9 harboured the trh gene indicating the presence of pathogenic V. parahaemolyticus. Our results show that mAb 4B10 sandwich ELISA developed in this study could be used as a rapid method for screening seafood samples for the presence of pathogenic V. parahaemolyticus.
机译:热稳定的直接溶血素(TDH)和TDH相关的溶血素(TRH)被认为是副溶血性弧菌的重要毒力因子,产生这两种或两者的菌株均被认为是致病性的。在这项研究中,我们生成了针对病原性副溶血性弧菌的纯化TRH重组蛋白的单克隆抗体(mAb)。与其他克隆相比,使用杂交瘤细胞克隆4B10的夹心酶联免疫吸附测定(ELISA)显示出更高的检测灵敏度。使用基于mAb 4B10的夹心ELISA,我们可以在41.18%(34个中的14个)海鲜样品中检测到致病性副溶血性弧菌。靶向toxR基因的PCR显示在64.7%(34个样本中的22个)海鲜样品中存在副溶血性弧菌。此外,针对毒力基因的PCR显示,有6个海鲜样品带有tdh基因,而9个带有trh基因,表明存在致病性副溶血性弧菌。我们的结果表明,在这项研究中开发的mAb 4B10夹心ELISA可以用作筛查海鲜样品中是否存在致病性副溶血性弧菌的快速方法。

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