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Standards for Methods Utilizing Environmental DNA for Detection of Fish Species

机译:利用环境DNA检测鱼类的方法标准

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摘要

Environmental DNA (eDNA) techniques are gaining attention as cost-effective, non-invasive strategies for acquiring information on fish and other aquatic organisms from water samples. Currently, eDNA approaches are used to detect specific fish species and determine fish community diversity. Various protocols used with eDNA methods for aquatic organism detection have been reported in different eDNA studies, but there are no general recommendations for fish detection. Herein, we reviewed 168 papers to supplement and highlight the key criteria for each step of eDNA technology in fish detection and provide general suggestions for eliminating detection errors. Although there is no unified recommendation for the application of diverse eDNA in detecting fish species, in most cases, 1 or 2 L surface water collection and eDNA capture on 0.7-μm glass fiber filters followed by extraction with a DNeasy Blood and Tissue Kit or PowerWater DNA Isolation Kit are useful for obtaining high-quality eDNA. Subsequently, species-specific quantitative polymerase chain reaction (qPCR) assays based on mitochondrial cytochrome b gene markers or eDNA metabarcoding based on both and markers via high-throughput sequencing can effectively detect target DNA or estimate species richness. Furthermore, detection errors can be minimized by mitigating contamination, negative control, PCR replication, and using multiple genetic markers. Our aim is to provide a useful strategy for fish eDNA technology that can be applied by researchers, advisors, and managers.
机译:作为一种经济有效的,非侵入性的策略,环境DNA(eDNA)技术可以从水样中获取有关鱼类和其他水生生物的信息。当前,eDNA方法用于检测特定鱼类并确定鱼类群落多样性。在不同的eDNA研究中,已经报道了eDNA方法用于水生生物检测的各种协议,但是没有关于鱼类检测的一般建议。在本文中,我们审查了168篇论文,以补充和强调eDNA技术在鱼类检测中每个步骤的关键标准,并为消除检测错误提供了一般性建议。尽管没有统一的建议将多种eDNA应用于检测鱼类,但在大多数情况下,在0.7-μm玻璃纤维滤池上收集1或2 L地表水并捕获eDNA,然后使用DNeasy血液和组织试剂盒或PowerWater进行提取DNA分离试剂盒可用于获得高质量的eDNA。随后,基于线粒体细胞色素b基因标志物或基于两者的eDNA metabarcoding和基于标志物的eDNA metabarcoding的物种特异性定量聚合酶链反应(qPCR)分析可通过高通量测序来有效检测目标DNA或估计物种丰富度。此外,通过减少污染,阴性对照,PCR复制和使用多种遗传标记,可以最大程度地减少检测错误。我们的目标是为鱼类eDNA技术提供一种有用的策略,以供研究人员,顾问和管理人员应用。

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