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MiFish, a set of universal PCR primers for metabarcoding environmental DNA from fishes: detection of more than 230 subtropical marine species

机译:MiFish,一套通用的PCR引物,用于对鱼类的环境DNA进行条形码编码:检测230多种亚热带海洋物种

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We developed a set of universal PCR primers (MiFish-U/E) for metabarcoding environmental DNA (eDNA) from fishes. Primers were designed using aligned whole mitochondrial genome (mitogenome) sequences from 880 species, supplemented by partial mitogenome sequences from 160 elasmobranchs (sharks and rays). The primers target a hypervariable region of the 12S rRNA gene (163–185?bp), which contains sufficient information to identify fishes to taxonomic family, genus and species except for some closely related congeners. To test versatility of the primers across a diverse range of fishes, we sampled eDNA from four tanks in the Okinawa Churaumi Aquarium with known species compositions, prepared dual-indexed libraries and performed paired-end sequencing of the region using high-throughput next-generation sequencing technologies. Out of the 180 marine fish species contained in the four tanks with reference sequences in a custom database, we detected 168 species (93.3%) distributed across 59 families and 123 genera. These fishes are not only taxonomically diverse, ranging from sharks and rays to higher teleosts, but are also greatly varied in their ecology, including both pelagic and benthic species living in shallow coastal to deep waters. We also sampled natural seawaters around coral reefs near the aquarium and detected 93 fish species using this approach. Of the 93 species, 64 were not detected in the four aquarium tanks, rendering the total number of species detected to 232 (from 70 families and 152 genera). The metabarcoding approach presented here is non-invasive, more efficient, more cost-effective and more sensitive than the traditional survey methods. It has the potential to serve as an alternative (or complementary) tool for biodiversity monitoring that revolutionizes natural resource management and ecological studies of fish communities on larger spatial and temporal scales.
机译:我们开发了一套通用的PCR引物(MiFish-U / E),用于鱼类的metabarcoding环境DNA(eDNA)。使用来自880个物种的完整线粒体基因组序列(有丝分裂基因组),加上来自160个弹性分支(鲨鱼和射线)的部分有丝分裂基因组序列,设计引物。这些引物靶向12S rRNA基因的一个高变区(163–185?bp),该区包含足够的信息以识别鱼类的分类学家族,属和物种,除了一些密切相关的同源物。为了测试引物在多种鱼类中的通用性,我们从冲绳美丽海水族馆四个鱼池中取样了已知物种组成的eDNA,准备了双索引文库,并使用高通量下一代测序技术对该区域进行了双末端测序测序技术。在一个自定义数据库中,在四个带有参考序列的鱼缸中包含的180种海洋鱼类中,我们检测到分布在59个科和123属中的168种(93.3%)。这些鱼类不仅在分类学上各不相同,从鲨鱼和rays鱼到更高的硬骨鱼,而且在生态方面也有很大差异,包括生活在浅海沿岸至深水域的浮游和底栖物种。我们还对水族馆附近珊瑚礁周围的天然海水进行了采样,并使用这种方法检测了93种鱼类。在这93个物种中,没有在四个水族箱中检测到64种,使被检测的物种总数达到232种(来自70个科和152属)。与传统的调查方法相比,此处介绍的元条形码方法是非侵入性的,效率更高,更具成本效益且更敏感。它有可能作为生物多样性监测的替代(或补充)工具,从而在更大的时空尺度上彻底改变自然资源管理和鱼类群落生态研究。

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