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用于检测五大湖入侵无脊椎动物物种的环境DNA(eDNA)宏条形码分析

Environmental DNA (eDNA) metabarcoding assays to detect invasive invertebrate species in the Great Lakes.

作者信息

Klymus Katy E, Marshall Nathaniel T, Stepien Carol A

机构信息

Great Lakes Genetics/Genomics Laboratory, Department of Environmental Sciences, University of Toledo, Toledo, OH, United States of America.

出版信息

PLoS One. 2017 May 18;12(5):e0177643. doi: 10.1371/journal.pone.0177643. eCollection 2017.

Abstract

Describing and monitoring biodiversity comprise integral parts of ecosystem management. Recent research coupling metabarcoding and environmental DNA (eDNA) demonstrate that these methods can serve as important tools for surveying biodiversity, while significantly decreasing the time, expense and resources spent on traditional survey methods. The literature emphasizes the importance of genetic marker development, as the markers dictate the applicability, sensitivity and resolution ability of an eDNA assay. The present study developed two metabarcoding eDNA assays using the mtDNA 16S RNA gene with Illumina MiSeq platform to detect invertebrate fauna in the Laurentian Great Lakes and surrounding waterways, with a focus for use on invasive bivalve and gastropod species monitoring. We employed careful primer design and in vitro testing with mock communities to assess ability of the markers to amplify and sequence targeted species DNA, while retaining rank abundance information. In our mock communities, read abundances reflected the initial input abundance, with regressions having significant slopes (p<0.05) and high coefficients of determination (R2) for all comparisons. Tests on field environmental samples revealed similar ability of our markers to measure relative abundance. Due to the limited reference sequence data available for these invertebrate species, care must be taken when analyzing results and identifying sequence reads to species level. These markers extend eDNA metabarcoding research for molluscs and appear relevant to other invertebrate taxa, such as rotifers and bryozoans. Furthermore, the sphaeriid mussel assay is group-specific, exclusively amplifying bivalves in the Sphaeridae family and providing species-level identification. Our assays provide useful tools for managers and conservation scientists, facilitating early detection of invasive species as well as improving resolution of mollusc diversity.

摘要

描述和监测生物多样性是生态系统管理的重要组成部分。最近将宏条形码技术与环境DNA(eDNA)相结合的研究表明,这些方法可作为生物多样性调查的重要工具,同时能显著减少传统调查方法所需的时间、费用和资源。文献强调了基因标记开发的重要性,因为标记决定了eDNA检测的适用性、灵敏度和分辨率。本研究利用Illumina MiSeq平台,基于线粒体DNA 16S rRNA基因开发了两种宏条形码eDNA检测方法,用于检测劳伦琴五大湖及周边水道中的无脊椎动物区系,重点是监测入侵双壳贝类和腹足类物种。我们精心设计引物,并使用模拟群落进行体外测试,以评估标记物扩增和测序目标物种DNA的能力,同时保留相对丰度信息。在我们的模拟群落中,读数丰度反映了初始输入丰度,所有比较的回归斜率均显著(p<0.05),决定系数(R2)较高。对野外环境样本的测试表明,我们的标记物在测量相对丰度方面具有相似的能力。由于这些无脊椎动物物种的参考序列数据有限,在分析结果并将序列读数鉴定到物种水平时必须谨慎。这些标记拓展了针对软体动物的eDNA宏条形码研究,并且似乎与其他无脊椎动物类群(如轮虫和苔藓虫)相关。此外,球蚬贻贝检测方法具有群体特异性,专门扩增球蚬科的双壳贝类,并提供物种水平的鉴定。我们的检测方法为管理人员和保护科学家提供了有用的工具,有助于早期发现入侵物种,并提高软体动物多样性的分辨率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a812/5436814/51b405cfcea2/pone.0177643.g001.jpg

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