从浮游生物样本中检测fortunelimnoperna DNA:一种新方法

Leandro Capurro, E. Brugnoli, E. Díaz-Ferguson, C. Martínez
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引用次数: 0

摘要

金贻贝是一种入侵性软体动物,原产于东南亚。在入侵的早期阶段,对L.fortunei的检测是一种有趣的控制和根除策略。为了达到这些目的,传统的方法是基于识别浮游动物或底栖动物群落样本中的物种。此外,还提出了基于检测不同环境样品中DNA(eDNA)的分子方法。我们描述并讨论了一种基于淡水系统浮游生物样本中线粒体eDNA检测L.fortunei的方案。2018-2019年期间,从乌拉圭里奥内格罗水电站的冷却系统中获得了水样。eDNA通过终止时间PCR检测,PCR产物在聚丙烯酰胺凝胶和银染上解析。引物特异性是在相关的湖沼和半咸水原生物种中确定的。敏感性分析为基因组DNA浓度和幼虫数量。测试了不同的方法从样品中去除抑制剂。最后,对eDNA PCR产物进行测序,以确认反应的特异性。分子技术得到的结果比传统的物种检测方法更灵敏。
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Detection of Limnoperna fortunei DNA From Plankton Samples: A New Protocol
Limnoperna fortunei (golden mussel) is an invasive mollusk, native to Southeast Asia. The detection of L. fortunei, during early stages of the invasion, is an interesting strategy for its control and eradication. For these aims, traditional methods are used based on identifying the species in samples of zooplankton or benthos community. In addition, molecular methods based on the detection of DNA in different environmental samples (eDNA) have been proposed. We describe and discuss a protocol developed for the detection of L. fortunei based on mitochondrial eDNA in plankton samples from freshwater systems. Water samples were obtained during 2018-2019, from cooling systems of the hydroelectric power plant in Río Negro, Uruguay. eDNA was detected by end-time PCR and PCR products were resolved on polyacrylamide gels and silver staining. Primers specificity was determined in related limnic and brackish native species. Sensitivity was analyzed as genomic DNA concentration and number of larvae. Different methodologies were tested to remove inhibitors from samples. Finally, the eDNA PCR products were sequenced to confirm the specificity of the reaction. The results obtained by molecular techniques were more sensitive than traditional methods of species detection.
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