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首页> 外文期刊>Analytica chimica acta >Detection and quantification of the toxic marine microalgae Karlodinium veneficum and Karlodinium armiger using recombinase polymerase amplification and enzyme-linked oligonucleotide assay
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Detection and quantification of the toxic marine microalgae Karlodinium veneficum and Karlodinium armiger using recombinase polymerase amplification and enzyme-linked oligonucleotide assay

机译:使用重组酶聚合酶扩增和酶联寡核苷酸测定检测和定量毒性海洋微藻karlodinium viseficum和karlodinium armiger

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摘要

Karlodinium is a dinoflagellate responsible for fish-killing events worldwide. In Alfacs Bay (NW Mediterranean Sea), the presence of two Karlodinium species (K. veneficum and K. armiger) with different toxicities has been reported. This work presents a method that combines recombinase polymerase amplification (RPA) with an enzyme-linked oligonucleotide assay (ELONA) to identify, discriminate and quantify these two species. The system was characterised using synthetic DNA and genomic DNA, and the specificity was confirmed by cross-reactivity experiments. Calibration curves were constructed using 10-fold dilutions of cultured cells, attaining a limit of detection of around 50,000 cells/L, far below the Karlodinium spp. alert threshold (200,000 cells/L). Finally, the assay was applied to spiked seawater samples, showing an excellent correlation with the spiking levels and light microscopy counts. This approach is more rapid, specific and user-friendly than traditional microscopy techniques, and shows great promise for the surveillance and management of harmful algal blooms. (C) 2018 Elsevier B.V. All rights reserved.
机译:Karlodinium是一种负责全球鱼类杀戮事件的恐龙。在Alfacs Bay(NW地中海)中,已经报道了两种具有不同毒性的karlodinium(K.veficum和K.Acriger)的存在。该工作介绍了一种方法,该方法将重组酶聚合酶扩增(RPA)与酶联寡核苷酸测定(ELONA)结合以鉴定,鉴别和量化这两个物种。使用合成DNA和基因组DNA表征该系统,并且通过交叉反应性实验证实了特异性。使用10倍稀释的细胞构建校准曲线,其检测约为50,000个细胞/ L的限制,远低于Karlodinium SPP。警报阈值(200,000个单元/ L)。最后,将测定施用于尖刺的海水样本,显示出与尖峰水平和光学显微镜计数的优异相关性。这种方法比传统的显微镜技术更快速,具体和用户友好,并且对有害藻类盛开的监督和管理表现出了很大的承诺。 (c)2018 Elsevier B.v.保留所有权利。

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