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样本混合在淡水鱼类群落环境 DNA 宏条形码分析中的作用和局限性。

Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities.

机构信息

Department of Environmental Solution Technology, Facility of Science & Technology, Ryukoku University, Seta-Oe, Otsu, 520-2194, Shiga, Japan.

Graduate School of Simulation Studies, University of Hyogo, Minatojima-minamimachi, Kobe, 650-0047, Japan.

出版信息

Sci Rep. 2017 Nov 1;7(1):14860. doi: 10.1038/s41598-017-14978-6.

DOI:10.1038/s41598-017-14978-6
PMID:29093520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5665893/
Abstract

Environmental DNA (eDNA) metabarcoding has been used increasingly to assess biodiversity of aquatic vertebrates. However, there still remains to be developed a sampling design of eDNA metabarcoding that can ensure high detection rates of species with minimum total survey effort, especially for large-scale surveys of aquatic organisms. We here tested whether pooling of eDNA samples can be used to evaluate biodiversity of freshwater fishes in four satellite lakes of Lake Biwa, Japan. Fish communities detected by eDNA metabarcoding of the mitochondrial 12S region were compared between the individual and pooled samples. In the individual samples, 31, 22, 33, and 31 fish lineages (proxies for species) were observed at the respective sites, within which moderate spatial autocorrelation existed. In the pooled samples, 30, 20, 29, and 27, lineages were detected, respectively, even after 15 PCR replicates. Lineages accounting for < 0.05% of the total read count of each site's individual samples were mostly undetectable in the pooled samples. Moreover, fish communities detected were similar among PCR replicates in the pooled samples. Because of the decreased detection rates, the pooling strategy is unsuitable for estimating fish species richness. However, this procedure is useful potentially for among-site comparison of representative fish communities.

摘要

环境 DNA (eDNA) 宏条形码技术已被越来越多地用于评估水生脊椎动物的生物多样性。然而,仍需要开发一种 eDNA 宏条形码采样设计,以确保在最小的总调查工作量下,具有高的物种检测率,特别是对于水生生物的大规模调查。在这里,我们测试了在日本琵琶湖的四个卫星湖中,是否可以通过汇集 eDNA 样本来评估淡水鱼类的生物多样性。比较了线粒体 12S 区 eDNA 宏条形码检测到的鱼类群落与个体和汇集样本之间的关系。在个体样本中,在各个地点分别观察到 31、22、33 和 31 个鱼类谱系(代表物种),其中存在中度的空间自相关。在汇集样本中,即使进行了 15 次 PCR 重复,也分别检测到 30、20、29 和 27 个谱系。在每个地点个体样本的总读取计数中占比<0.05%的谱系大多在汇集样本中无法检测到。此外,汇集样本中的 PCR 重复检测到的鱼类群落相似。由于检测率降低,汇集策略不适合估计鱼类物种丰富度。但是,这种方法对于代表性鱼类群落的站点间比较可能是有用的。

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