Harper Lynsey R, Lawson Handley Lori, Hahn Christoph, Boonham Neil, Rees Helen C, Gough Kevin C, Lewis Erin, Adams Ian P, Brotherton Peter, Phillips Susanna, Hänfling Bernd
School of Environmental Sciences University of Hull Hull UK.
Institute of Zoology University of Graz Graz Styria Austria.
Ecol Evol. 2018 May 29;8(12):6330-6341. doi: 10.1002/ece3.4013. eCollection 2018 Jun.
Environmental DNA (eDNA) analysis is a rapid, cost-effective, non-invasive biodiversity monitoring tool which utilises DNA left behind in the environment by organisms for species detection. The method is used as a species-specific survey tool for rare or invasive species across a broad range of ecosystems. Recently, eDNA and "metabarcoding" have been combined to describe whole communities rather than focusing on single target species. However, whether metabarcoding is as sensitive as targeted approaches for rare species detection remains to be evaluated. The great crested newt is a flagship pond species of international conservation concern and the first UK species to be routinely monitored using eDNA. We evaluate whether eDNA metabarcoding has comparable sensitivity to targeted real-time quantitative PCR (qPCR) for detection. Extracted eDNA samples ( = 532) were screened for by qPCR and analysed for all vertebrate species using high-throughput sequencing technology. With qPCR and a detection threshold of 1 of 12 positive qPCR replicates, newts were detected in 50% of ponds. Detection decreased to 32% when the threshold was increased to 4 of 12 positive qPCR replicates. With metabarcoding, newts were detected in 34% of ponds without a detection threshold, and in 28% of ponds when a threshold (0.028%) was applied. Therefore, qPCR provided greater detection than metabarcoding but metabarcoding detection with no threshold was equivalent to qPCR with a stringent detection threshold. The proportion of sequences in each sample was positively associated with the number of positive qPCR replicates (qPCR score) suggesting eDNA metabarcoding may be indicative of eDNA concentration. eDNA metabarcoding holds enormous potential for holistic biodiversity assessment and routine freshwater monitoring. We advocate this community approach to freshwater monitoring to guide management and conservation, whereby entire communities can be initially surveyed to best inform use of funding and time for species-specific surveys.
环境DNA(eDNA)分析是一种快速、经济高效的非侵入性生物多样性监测工具,它利用生物体留在环境中的DNA进行物种检测。该方法被用作一种针对广泛生态系统中稀有或入侵物种的特定物种调查工具。最近,eDNA和“宏条形码”已被结合起来描述整个群落,而不是专注于单一目标物种。然而,宏条形码在稀有物种检测方面是否与靶向方法一样敏感仍有待评估。大冠蝾螈是一种具有国际保护意义的旗舰池塘物种,也是英国首个使用eDNA进行常规监测的物种。我们评估了eDNA宏条形码在检测方面是否与靶向实时定量PCR(qPCR)具有可比的灵敏度。提取的eDNA样本(n = 532)通过qPCR筛选是否存在大冠蝾螈,并使用高通量测序技术分析所有脊椎动物物种。使用qPCR且检测阈值为12个阳性qPCR重复样本中的1个时,在50%的池塘中检测到了蝾螈。当阈值增加到12个阳性qPCR重复样本中的4个时,检测率降至32%。使用宏条形码时,在没有检测阈值的情况下,34%的池塘中检测到了蝾螈,应用阈值(0.028%)时,在28%的池塘中检测到了蝾螈。因此,qPCR提供了比宏条形码更高的检测率,但无阈值的宏条形码检测等同于具有严格检测阈值的qPCR。每个样本中的大冠蝾螈序列比例与阳性qPCR重复样本数量(qPCR分数)呈正相关,这表明eDNA宏条形码可能指示eDNA浓度。eDNA宏条形码在整体生物多样性评估和常规淡水监测方面具有巨大潜力。我们提倡这种用于淡水监测的群落方法来指导管理和保护工作,即可以先对整个群落进行调查,以便为物种特定调查的资金和时间使用提供最佳信息。