Wilcox Taylor M, Carim Kellie J, McKelvey Kevin S, Young Michael K, Schwartz Michael K
United States Department of Agriculture, Forest Service, National Genomics Center for Wildlife and Fish Conservation, Rocky Mountain Research Station, Missoula, Montana, United States of America.
University of Montana, Division of Biological Sciences, 32 Campus Dr., Missoula, Montana, United States of America.
PLoS One. 2015 Nov 4;10(11):e0142008. doi: 10.1371/journal.pone.0142008. eCollection 2015.
Environmental DNA (eDNA) sampling is a powerful tool for detecting invasive and native aquatic species. Often, species of conservation interest co-occur with other, closely related taxa. Here, we developed qPCR (quantitative PCR) markers which distinguish westslope cutthroat trout (Oncorhynchus clarkii lewsi), Yellowstone cutthroat trout (O. clarkii bouvieri), and rainbow trout (O. mykiss), which are of conservation interest both as native species and as invasive species across each other's native ranges. We found that local polymorphisms within westslope cutthroat trout and rainbow trout posed a challenge to designing assays that are generally applicable across the range of these widely-distributed species. Further, poorly-resolved taxonomies of Yellowstone cutthroat trout and Bonneville cutthroat trout (O. c. utah) prevented design of an assay that distinguishes these recognized taxa. The issues of intraspecific polymorphism and unresolved taxonomy for eDNA assay design addressed in this study are likely to be general problems for closely-related taxa. Prior to field application, we recommend that future studies sample populations and test assays more broadly than has been typical of published eDNA assays to date.
环境DNA(eDNA)采样是检测入侵性和本地水生物种的有力工具。通常,具有保护意义的物种与其他密切相关的分类群共存。在此,我们开发了定量聚合酶链反应(qPCR)标记,以区分西部斜坡割喉鳟(Oncorhynchus clarkii lewsi)、黄石割喉鳟(O. clarkii bouvieri)和虹鳟(O. mykiss),这些物种作为本地物种以及在彼此原生范围内的入侵物种都具有保护意义。我们发现,西部斜坡割喉鳟和虹鳟的局部多态性对设计适用于这些广泛分布物种的检测方法构成了挑战。此外,黄石割喉鳟和邦纳维尔割喉鳟(O. c. utah)的分类不够明确,这使得无法设计出区分这些公认分类群的检测方法。本研究中解决的eDNA检测设计中的种内多态性和分类不明确问题,可能是密切相关分类群普遍存在的问题。在实地应用之前,我们建议未来的研究比迄今为止已发表的eDNA检测方法更广泛地对种群进行采样并测试检测方法。