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Development of environmental DNA (eDNA) methods for detecting high-risk freshwater fishes in live trade in Canada

机译:在加拿大实时贸易中检测高危淡水鱼的环境DNA(EDNA)方法的开发

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摘要

Preventing the arrival, establishment, and spread of aquatic invasive species is an important step in protecting our aquatic environments. The use of detection tools, like DNA barcoding technologies, high-throughput sequencing and environmental DNA (eDNA) monitoring, is becoming increasingly important in preventing the introduction of potential invasive species. The combination of eDNA with realtime PCR (qPCR) provide the opportunity to have a rapid and specific detection. In this study, we developed a DNA sequence library that has sufficient depth and species coverage such that high-risk species can be confidently discriminated from legitimately imported and native species. A total of 12 species-specific qPCR assays were developed for the detection of 13 potential invasive species (pAIS) in bulk water samples. Detection of these species was also compared with a HTS approach. We have demonstrated the high sensitivity of qPCR assays using eDNA at very low densities, suggesting we could detect a low number of individuals mixed with non-target species in a simulated live shipment. For the detection of a targeted list of species, qPCR is advantageous. The mini-barcodes developed in this project offered a good sensitivity of detection, and HTS is a discovery tool that can be desirable when unlisted or numerous species need to be identified.
机译:防止水生侵入物种的到达,建立和传播是保护水产环境的重要一步。使用检测工具,如DNA条形码技术,高通量测序和环境DNA(EDNA)监测,在预防潜在的侵入性物种的引入时变得越来越重要。 EDNA与实时PCR(QPCR)的组合提供了具有快速和特异性检测的机会。在这项研究中,我们开发了一种DNA序列文库,具有足够的深度和物种覆盖,使得能够自信地歧视高风险物种。共开发了12种特异性QPCR测定,用于检测散装水样中的13种潜在侵入物种(PAI)。还与HTS方法进行比较了这些物种的检测。我们已经证明了使用eDNA在非常低密度的QPCR测定的高灵敏度,这表明我们可以在模拟实时发货中检测与非目标物种混合的少数个体。为了检测目标物种列表,QPCR是有利的。该项目中开发的迷你条形码提供了良好的检测敏感性,HTS是一种发现工具,当需要识别出未列出或许多物种时,可能是可取的。

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