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Development of a SYBR Green I real-time PCR for quantitative detection of Vibrio alginolyticus in seawater and seafood

机译:开发用于定量检测海水和海鲜中溶藻弧菌的SYBR Green I实时PCR

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摘要

Vibrio alginolyticus is an economically important micro-organism. The main aim of the present study was to develop a real-time polymerase chain reaction (PCR) assay for rapid, sensitive and effective quantification of V. alginolyticus in seawater and seafood. Purified DNA of V. alginolyticus, artificially inoculated seawater and seafood tissue homogenates were subjected to the gyrB-targeted real-time PCR assay. Natural seawater and seafood samples were analysed by this real-time PCR protocol. Specificity tests showed that positive result was obtained only with V. alginolyticus strains. The detection sensitivity was determined to be 0p"4 pg of genomic DNA equivalent to 72 cells per PCR in pure culture and 100 cells in 1 ml of seawater or seafood tissue homogenates. Single cell detection is achieved after 3 h of sample enrichment. A sensitive and specific SYBR Green I-based real-time PCR assay targeting gyrB gene was successfully developed to quantify V. alginolyticus within 6 h in seawater and seafood samples. No report on the molecular-based method was available for quantitative detection of V. alginolyticus. This work will provide a novel method for evaluation of the risk of V. alginolyticus to marine environmental health and seafood safety.
机译:溶藻弧菌是一种经济上重要的微生物。本研究的主要目的是开发一种实时聚合酶链反应(PCR)分析方法,用于快速,灵敏和有效地定量海水和海鲜中的溶藻弧菌。对溶藻弧菌,人工接种的海水和海鲜组织匀浆的纯化DNA进行了针对gyrB的实时PCR分析。通过此实时PCR方案分析了天然海水和海鲜样品。特异性测试表明,仅溶藻弧菌菌株获得阳性结果。确定的检测灵敏度为0p“ 4 pg基因组DNA,相当于纯培养中每个PCR 72个细胞,以及1 ml海水或海鲜组织匀浆中的100个细胞。样品富集3 h后即可实现单细胞检测。并成功开发了以gyBRB基因为基础的基于SYBR Green I的实时PCR检测方法,用于定量检测海水和海产品中6小时内的溶藻弧菌。这项工作将为评估溶藻弧菌对海洋环境健康和海鲜安全的风险提供一种新颖的方法。

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