Environmental DNA storage and extraction method affects detectability for multiple aquatic invasive species

Q1 Agricultural and Biological Sciences Environmental DNA Pub Date : 2024-05-07 DOI:10.1002/edn3.557
Samantha M. García, Chan Lan Chun, Josh Dumke, Gretchen J. A. Hansen, Kathleen B. Quebedeaux, Christopher Rounds, Anna Totsch, Eric R. Larson
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Abstract

Environmental DNA (eDNA) refers to genetic material released by organisms into their surrounding environment. Collecting and identifying eDNA has gained popularity for monitoring and surveillance of aquatic invasive species. Invasive species management is most successful when an invasion is identified early while population size is likely to be low, highlighting the importance of eDNA detection sensitivity. Various factors influence DNA yield recovered from environmental samples. Environmental DNA storage and extraction methods, for example, can be adjusted to maximize DNA yield, thereby improving detectability. In this study, we compared the performance of two eDNA storage and extraction methods in detecting three common aquatic invasive species (Bythotrephes longimanus, Dreissena polymorpha, and Faxonius rusticus) across five natural ecosystems of Minnesota, United States. One method involved storing filters in 95% ethanol (EtOH) and extracting DNA using a DNeasy PowerSoil Pro Kit (Qiagen, Hilden, Germany), whereas the other method used cetyl trimethylammonium bromide (CTAB) for storage and a phenol–chloroform–isoamyl (PCI) procedure for DNA extraction. We also investigated the effect of DNA extract volume (1 μL relative to 3 μL) in qPCR reactions on eDNA detections for the commercial kit method. The CTAB-PCI method yielded significantly more positive detections, across all three species, compared to the EtOH-Qiagen method. Moreover, we found that using 1 μL of DNA extract in qPCR reactions was equally effective as using 3 μL. To improve detections of aquatic invasive species, we recommend that researchers store eDNA sample filters in CTAB or a similar lysis buffer such as Longmire's solution and extract with PCI when feasible, but note that lower extract volumes might be used without negative effect when either increasing technical replicates or repurposing samples for the detection of multiple species.

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环境 DNA 储存和提取方法会影响多种水生入侵物种的可检测性
环境 DNA(eDNA)是指生物体释放到周围环境中的遗传物质。收集和鉴定 eDNA 在监测和监视水生入侵物种方面越来越受欢迎。入侵物种管理最成功的方法是在种群数量可能较低时及早发现,这就凸显了 eDNA 检测灵敏度的重要性。影响从环境样本中回收 DNA 产量的因素有很多。例如,环境 DNA 的储存和提取方法可以通过调整使 DNA 产量最大化,从而提高检测灵敏度。在这项研究中,我们比较了两种 eDNA 储存和提取方法在检测美国明尼苏达州五个自然生态系统中三种常见水生入侵物种(Bythotrephes longimanus、Dreissena polymorpha 和 Faxonius rusticus)方面的性能。一种方法是将过滤器储存在 95% 的乙醇(EtOH)中,然后使用 DNeasy PowerSoil Pro Kit(Qiagen,德国希尔登)提取 DNA,而另一种方法是使用十六烷基三甲基溴化铵(CTAB)进行储存,并使用苯酚-氯仿-异戊基(PCI)程序提取 DNA。我们还研究了 qPCR 反应中 DNA 提取液体积(1 μL 相对于 3 μL)对商用试剂盒方法检测 eDNA 的影响。与 EtOH-Qiagen 方法相比,CTAB-PCI 方法在所有三个物种中的阳性检测率都要高得多。此外,我们还发现,在 qPCR 反应中使用 1 μL DNA 提取液与使用 3 μL 的效果相同。为了提高水生入侵物种的检测效果,我们建议研究人员将 eDNA 样品过滤器储存在 CTAB 或类似的裂解缓冲液(如 Longmire's 溶液)中,并在可行的情况下使用 PCI 进行提取,但要注意的是,在增加技术重复次数或重新利用样品检测多个物种时,使用较低的提取量也不会产生负面影响。
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来源期刊
Environmental DNA
Environmental DNA Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
11.00
自引率
0.00%
发文量
99
审稿时长
16 weeks
期刊最新文献
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