Nichols Ruth V, Curd Emily, Heintzman Peter D, Shapiro Beth
Department of Ecology and Evolutionary Biology, University of California Santa Cruz, Santa Cruz, CA, USA.
Department of Ecology and Evolutionary Biology, University of California Los Angeles, Los Angeles, CA, USA.
Methods Mol Biol. 2019;1963:149-161. doi: 10.1007/978-1-4939-9176-1_16.
All organisms release their DNA into the environment through processes such as excretion and the senescence of tissues and limbs. This DNA, often referred to as environmental DNA (eDNA) or sedimentary ancient DNA (sedaDNA), can be recovered from both present-day and ancient soils, fecal samples, bodies of water and lake cores, and even air. While eDNA is a potentially useful record of past and present biodiversity, several challenges complicate data generation and interpretation of results. Most importantly, eDNA samples tend to be highly taxonomically mixed, and the target organism or group of organisms may be present at very low abundance within this mixture. To overcome this challenge, enrichment approaches are often used to target specific taxa of interest. Here, we describe a protocol to amplify metabarcodes or short, variable loci that identify lineages within broad taxonomic groups (e.g., plants, mammals), using the polymerase chain reaction (PCR) with established generic "barcode" primers. We also provide a catalog of animal and plant barcode primers that, because they target relatively short fragments of DNA, are potentially suitable for use with degraded DNA.
所有生物都会通过排泄以及组织和肢体衰老等过程将其DNA释放到环境中。这种DNA通常被称为环境DNA(eDNA)或沉积古DNA(sedaDNA),可以从现代和古代土壤、粪便样本、水体和湖泊岩芯甚至空气中获取。虽然eDNA是过去和现在生物多样性的潜在有用记录,但有几个挑战使数据生成和结果解读变得复杂。最重要的是,eDNA样本在分类学上往往高度混合,目标生物或生物群体在这种混合物中的丰度可能非常低。为了克服这一挑战,富集方法经常被用于针对特定的目标分类群。在这里,我们描述了一种使用聚合酶链反应(PCR)和已建立的通用“条形码”引物来扩增元条形码或短的可变基因座的方案,这些基因座可识别广泛分类群(如植物、哺乳动物)中的谱系。我们还提供了一个动植物条形码引物目录,由于它们针对相对较短的DNA片段,因此可能适用于降解的DNA。