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基于探针的多重实时 PCR 检测方法的开发和验证,用于快速准确地检测淡水鱼类物种。

Development and validation of probe-based multiplex real-time PCR assays for the rapid and accurate detection of freshwater fish species.

机构信息

Laurentian University, Department of Biology, Ontario, Canada.

Northern Ontario School of Medicine, Medical Sciences Division, Ontario, Canada.

出版信息

PLoS One. 2019 Jan 30;14(1):e0210165. doi: 10.1371/journal.pone.0210165. eCollection 2019.

Abstract

Reliable species identification methods are important for industrial environmental monitoring programs. Probe based real-time quantitative polymerase chain reaction (qPCR) provides an accurate, cost-effective and high-throughput method for species identification. Here we present the development and validation of species-specific primers and probes for the cytochrome c oxidase (COI) gene for the identification of eight ecologically and economically important freshwater fish species: lake whitefish (Coregonus clupeaformis), yellow perch (Perca flavescens), rainbow smelt (Osmerus mordax), brook trout (Salvelinus fontinalis), smallmouth bass (Micropterus dolomieu), round whitefish (Prosopium cylindraceum), spottail shiner (Notropis hudsonius) and deepwater sculpin (Myoxocephalus thompsonii). In order to identify novel primer-probe sets with maximum species-specificity, two separate primer-probe design criteria were employed. Highest ranked primer-probe sets from both methods were assayed to identify sequences that demonstrated highest specificity. Specificity was determined using control species from same genus and non-target species from different genus. Selected primer-probe sets were optimized for annealing temperature and primer-probe concentrations to identify minimum reagent parameters. The selected primer-probe sets were highly sensitive, with DNA concentrations as low as 1 ng adequate for positive species identification. A decoder algorithm was developed based on the cumulative qPCR results that allowed for full automation of species identification. Blinded experiments revealed that the combination of the species-specific primer/probes sets with the automated species decoder resulted in target species identification with 100% accuracy. We also conducted a cost/time comparison analysis between the qPCR assays established in this study with other species identification methods. The qPCR technique was the most cost-effective and least time consuming method of species identification. In summary, probe-based multiplex qPCR assays provide a rapid and accurate method for freshwater fish species identification, and the methodology established in this study can be utilized for various other species identification initiatives.

摘要

可靠的物种鉴定方法对工业环境监测计划至关重要。基于探针的实时定量聚合酶链反应 (qPCR) 为物种鉴定提供了一种准确、经济高效且高通量的方法。在这里,我们为细胞色素 c 氧化酶 (COI) 基因开发和验证了用于鉴定 8 种具有生态和经济重要性的淡水鱼类物种的特异性引物和探针:湖白鲑 (Coregonus clupeaformis)、黄鲈 (Perca flavescens)、虹鳟 (Osmerus mordax)、溪红点鲑 (Salvelinus fontinalis)、小口黑鲈 (Micropterus dolomieu)、圆白鲑 (Prosopium cylindraceum)、斑点闪光鲦 (Notropis hudsonius) 和深海杜父鱼 (Myoxocephalus thompsonii)。为了用最大的物种特异性识别新的引物-探针组,采用了两种独立的引物-探针设计标准。从这两种方法中获得的排名最高的引物-探针组用于鉴定表现出最高特异性的序列。特异性通过使用来自同一属的对照物种和来自不同属的非目标物种来确定。选择的引物-探针组针对退火温度和引物-探针浓度进行了优化,以确定最小的试剂参数。选择的引物-探针组非常灵敏,DNA 浓度低至 1ng 即可进行阳性物种鉴定。根据累积 qPCR 结果开发了一种解码器算法,允许完全自动化物种鉴定。盲测实验表明,将特异性引物/探针组与自动物种解码器相结合,可实现 100%准确的目标物种鉴定。我们还对本研究中建立的 qPCR 测定法与其他物种鉴定方法进行了成本/时间比较分析。qPCR 技术是最具成本效益且耗时最少的物种鉴定方法。总之,基于探针的多重 qPCR 检测为淡水鱼类物种鉴定提供了一种快速准确的方法,本研究中建立的方法可用于各种其他物种鉴定计划。

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