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捕获水生环境 DNA 的富集:初步概念验证。

Capture enrichment of aquatic environmental DNA: A first proof of concept.

机构信息

Rocky Mountain Research Station, National Genomics Center for Wildlife and Fish Conservation, U.S. Department of Agriculture, Forest Service, Missoula, Montana.

University of Montana, W.A. Franke College of Forestry & Conservation, Missoula, Montana.

出版信息

Mol Ecol Resour. 2018 Nov;18(6):1392-1401. doi: 10.1111/1755-0998.12928. Epub 2018 Aug 11.

Abstract

Environmental DNA (eDNA) sampling-the detection of genetic material in the environment to infer species presence-has rapidly grown as a tool for sampling aquatic animal communities. A potentially powerful feature of environmental sampling is that all taxa within the habitat shed DNA and so may be detectable, creating opportunity for whole-community assessments. However, animal DNA in the environment tends to be comparatively rare, making it necessary to enrich for genetic targets from focal taxa prior to sequencing. Current metabarcoding approaches for enrichment rely on bulk amplification using conserved primer annealing sites, which can result in skewed relative sequence abundance and failure to detect some taxa because of PCR bias. Here, we test capture enrichment via hybridization as an alternative strategy for target enrichment using a series of experiments on environmental samples and laboratory-generated, known-composition DNA mixtures. Capture enrichment resulted in detecting multiple species in both kinds of samples, and postcapture relative sequence abundance accurately reflected initial relative template abundance. However, further optimization is needed to permit reliable species detection at the very low-DNA quantities typical of environmental samples (<0.1 ng DNA). We estimate that our capture protocols are comparable to, but less sensitive than, current PCR-based eDNA analyses.

摘要

环境 DNA(eDNA)采样——通过检测环境中的遗传物质来推断物种的存在——已迅速成为一种用于采样水生动物群落的工具。环境采样的一个潜在强大特征是,栖息地内的所有分类群都会释放 DNA,因此都可能被检测到,从而为整个群落评估创造了机会。然而,环境中的动物 DNA 通常相对较少,因此在进行测序之前,有必要从焦点分类群中富集遗传目标。目前用于富集的代谢组学方法依赖于使用保守引物退火位点的批量扩增,这可能导致相对序列丰度的偏斜和由于 PCR 偏差而无法检测到某些分类群。在这里,我们通过杂交测试了捕获富集作为一种替代策略,用于使用一系列环境样本和实验室生成的已知组成 DNA 混合物的目标富集。捕获富集导致在这两种类型的样本中都检测到了多个物种,并且捕获后的相对序列丰度准确反映了初始相对模板丰度。然而,需要进一步优化,以允许在环境样本中典型的非常低的 DNA 量(<0.1 ng DNA)下进行可靠的物种检测。我们估计我们的捕获方案与基于 PCR 的当前 eDNA 分析相当,但敏感性低于后者。

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