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

机译:样品池在淡水鱼群落环境DNA元条形码中的作用和局限性

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摘要

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.
机译:环境DNA(eDNA)元条形码已越来越多地用于评估水生脊椎动物的生物多样性。但是,仍需要开发一种eDNA元条形码的采样设计,以确保以最小的总调查工作量就可以实现较高的物种检出率,尤其是对于大规模水生生物调查而言。我们在这里测试了eDNA样本池是否可用于评估日本琵琶湖四个卫星湖中淡水鱼的生物多样性。比较了单个样本和合并样本中通过线粒体12S区的eDNA metabarcoding检测到的鱼类群落。在各个样本中,在各个站点中观察到31、22、33和31条鱼谱系(物种的代表),在这些谱系中存在适度的空间自相关。即使在15次PCR复制后,在合并的样本中分别检测到30、20、29和27个谱系。占每个站点单个样本总阅读计数的<0.05%的谱系在合并的样本中大部分无法检测到。此外,在合并样本中的PCR复制品中,检测到的鱼类群落相似。由于检出率降低,因此合并策略不适合估计鱼类物种的丰富度。但是,该程序对于代表性鱼类群落的现场比较可能很有用。

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