Commonwealth Scientific and Industrial Research Organisation Land and Water , General Post Office Box 1700, Canberra , Australian Capital Territory 2601 , Australia.
Environ Sci Technol. 2018 Jun 5;52(11):6408-6416. doi: 10.1021/acs.est.8b01071. Epub 2018 May 24.
Environmental DNA (eDNA) is increasingly used to monitor aquatic macrofauna. Typically, short mitochondrial DNA fragments are targeted because these should be relatively more abundant in the environment as longer fragments will break into smaller fragments over time. However, longer fragments may permit more flexible primer design and increase taxonomic resolution for eDNA metabarcoding analyses, and recent studies have shown that long mitochondrial eDNA fragments can be extracted from environmental water samples. Nuclear eDNA fragments have also been proposed as targets, but little is known about their persistence in the aquatic environment. Here we measure the abundance of mitochondrial eDNA fragments of different lengths and of short nuclear eDNA fragments, originating from captive fish in experimental tanks, and we test whether longer mitochondrial and short nuclear fragments decay faster than short mitochondrial fragments following fish removal. We show that when fish are present, shorter mitochondrial fragments are more abundant in water samples than both longer mitochondrial fragments and short nuclear eDNA fragments. However, the rate of decay following fish removal was similar for all fragment types, suggesting that the differences in abundance resulted from differences in the rates at which different fragment types were produced rather than differences in their decay rates.
环境 DNA(eDNA)正越来越多地用于监测水生大型动物。通常情况下,人们会将目标锁定在较短的线粒体 DNA 片段上,因为随着时间的推移,较长的片段会断裂成更小的片段,因此这些片段在环境中应该更为丰富。然而,较长的片段可能会允许更灵活的引物设计,并提高 eDNA 宏条形码分析的分类分辨率,最近的研究表明,从环境水样中可以提取到长的线粒体 eDNA 片段。核 DNA 片段也被提议作为目标,但人们对其在水生环境中的持久性知之甚少。在这里,我们测量了来自实验水箱中圈养鱼类的不同长度的线粒体 DNA 片段和短核 DNA 片段的丰度,并测试了在鱼类移除后,较长的线粒体和短核片段是否比短的线粒体片段更快衰减。我们发现,当鱼类存在时,水样中较短的线粒体片段比长的线粒体片段和短核 eDNA 片段更为丰富。然而,鱼类移除后所有片段类型的衰减速率相似,这表明丰度的差异是由于不同片段类型的产生速率不同,而不是其衰减速率的差异所致。