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Dual quantitative PCR assay for identification and enumeration of Karlodinium veneficum and Karlodinium armiger combined with a simple and rapid DNA extraction method

机译:用于鉴定和枚举Karlodinium Veneficum和Karlodinium Armiger的双定量PCR测定与一种简单快速的DNA提取方法结合

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摘要

Karlodinium is a dinoflagellate genus responsible for massive fish mortality events worldwide. It is commonly found in Alfacs Bay (NW Mediterranean Sea), where the presence of two Karlodinium species (K. veneficum and K. armiger) with different toxicities has been reported. Microscopy analysis is not able to differentiate between these two species. Therefore, new and rapid methods that accurately and specifically detect and differentiate these two species are crucial to facilitate routine monitoring, to provide early warnings and to study population dynamics. In this work, a quantitative real-time PCR (qPCR) method to detect and enumerate K. veneficum and K. armiger is presented. The ITS1 region of the ribosomal DNA was used to design species-specific primers. The specificity of the primers together with the melting curve profile provided a reliable qualitative identification and discrimination between the two Karlodinium species. Additionally, a simple and rapid DNA extraction method was used. Standard curves were constructed from 10-fold dilutions of cultured microalgae cells. Finally, the applicability of the assay was tested with field samples collected from Alfacs Bay. Results showed a significant correlation between qPCR determinations and light microscopy counts (y = 2.838 x + 564; R (2) = 0.936). Overall, the qPCR method developed herein is specific, rapid, accurate, and promising for the detection of these two Karlodinium species in environmental samples.
机译:Karlodinium是一种恐龙属的属,负责全球巨大的鱼死亡事件。它通常在Alfacs Bay(NW地中海)中发现,其中报道了两种具有不同毒性的karlodinium(k.veficum和armiger)的存在。显微镜分析无法区分这两个物种。因此,准确且特别地检测和区分这两个物种的新和快速方法对于促进常规监测至关重要,以提供早期警告和研究人口动态。在这项工作中,提出了一种定量的实时PCR(QPCR)方法来检测和枚举K.Veficum和K.Armiger。核糖体DNA的其1区域用于设计特异性底漆。引物的特异性与熔化曲线曲线一起提供了两种卡洛蒽喹匹粒之间的可靠性定性鉴定和辨别。另外,使用简单且快速的DNA提取方法。标准曲线由10倍稀释的微藻细胞构成。最后,测试了测定的适用性用从阿尔法斯湾收集的田间样品进行测试。结果显示QPCR测定和光学显微镜计数之间的显着相关性(Y = 2.838 x + 564; R(2)= 0.936)。总体而言,本文开发的QPCR方法是针对在环境样品中检测这两种karlodinium物种的特异性,快速,准确,并且有希望。

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