Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Southwest University School of Life Sciences, Chongqing 400715, China.
Department of Evolutionary Genetics, Leibniz-Institute for Zoo and Wildlife Research, 10315 Berlin, Germany.
Genes (Basel). 2020 Mar 11;11(3):296. doi: 10.3390/genes11030296.
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.
环境 DNA(eDNA)技术作为一种经济有效的非侵入性策略,正在引起人们的关注,可用于从水样中获取鱼类和其他水生生物的信息。目前,eDNA 方法用于检测特定的鱼类物种和确定鱼类群落的多样性。在不同的 eDNA 研究中,已经报道了用于水生生物检测的各种 eDNA 方法的协议,但对于鱼类检测没有一般的建议。在此,我们回顾了 168 篇论文,以补充和强调鱼类检测中 eDNA 技术各个步骤的关键标准,并提供消除检测误差的一般建议。虽然没有针对不同 eDNA 应用于鱼类物种检测的统一建议,但在大多数情况下,采集 1 或 2 L 地表水,并用 0.7-μm 玻璃纤维过滤器捕获 eDNA,然后用 DNeasy Blood 和 Tissue Kit 或 PowerWater DNA 提取试剂盒进行提取,对于获得高质量的 eDNA 是有用的。随后,可以使用基于线粒体细胞色素 b 基因标记的特异性定量聚合酶链反应(qPCR)检测,或者通过高通量测序对 和 标记进行 eDNA 宏条形码检测,有效地检测目标 DNA 或估计物种丰富度。此外,通过减轻污染、阴性对照、PCR 复制和使用多个遗传标记,可以最大限度地减少检测误差。我们的目标是为鱼类 eDNA 技术提供一种有用的策略,供研究人员、顾问和管理者应用。