首页> 外文期刊>Applied Microbiology and Biotechnology >Multiplex polymerase chain reaction-based assay for the specific detection of toxin-producing Vibrio cholerae in fish and fishery products
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Multiplex polymerase chain reaction-based assay for the specific detection of toxin-producing Vibrio cholerae in fish and fishery products

机译:基于多重聚合酶链反应的检测可用于鱼和渔产品中产毒素的霍乱弧菌的特异性检测

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摘要

A multiplex polymerase chain reaction (MPCR)-based assay was developed for the simultaneous detection of Vibrios using the genus-specific RNA polymerase subunit A (rpoA) gene and specific detection of toxin-producing Vibrio cholerae strains using two sets of primer based on cholera toxin subunit A (ctxA) and repeat in toxin subunit A (RtxA)-producing genes. The MPCR method developed is applicable to both the simultaneous and the two-step detection of genus Vibrio total and toxigenic V. cholerae species. This assay was specific as no amplification occurred with the other bacterial pathogens tested. The sensitivity of the assay was tested by artificially spiking the shrimp homogenate with the toxigenic strain of V. cholerae (NICED 16582) in different dilutions. The developed MPCR assay could detect three cells of V. cholerae in 12 h pre-enrichment in APW. The proposed method is rapid, sensitive, and specific for the detection of Vibrio genus as well as toxin-producing V. cholerae strains in environmental samples.
机译:开发了一种基于多重聚合酶链反应(MPCR)的检测方法,用于同时使用属特异性RNA聚合酶亚基A(rpoA)基因检测弧菌,并使用两组基于霍乱的引物同时检测产毒素的霍乱弧菌菌株毒素亚基A(ctxA),并在产生毒素亚基A(RtxA)的基因中重复。所开发的MPCR方法适用于总弧菌属和产霍乱弧菌物种的同时和两步检测。该试验具有特异性,因为在测试的其他细菌病原体中未发生扩增。通过用不同稀释度的霍乱弧菌产毒菌株(NICED 16582)人工加标虾匀浆来测试测定的灵敏度。所开发的MPCR分析法可以在APW中预富集12 h时检测到霍乱弧菌的三个细胞。所提出的方法是快速,灵敏的,并且特异性地用于检测环境样品中的弧菌属以及产毒素的霍乱弧菌。

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