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Metagenomic sequencing of environmental DNA reveals marine faunal assemblages from the West Antarctic Peninsula

机译:环境DNA的Metagenomic测序揭示了来自西南极半岛的海洋动物群组合

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The West Antarctic Peninsula (WAP) is the fastest warming region in Antarctica where climate impact on the cold-adapted marine ecosystem is already visible. To monitor faunal changes in remote vast bodies of Antarctic waters, efficient and informative tools are essential. High-throughput sequencing of environmental DNA (eDNA) has emerged as one such tool for monitoring biodiversity and ecosystems, as it increases detection sensitivity of taxa, and sampling is often simpler and less costly than traditional collection methods. We collected water samples from four WAP shallow (<= 300 m) shelf regions, recovered the eDNA therein, and performed metagenomic shotgun sequencing and analyses to determine the effectiveness of this method to assess marine benthic faunal diversity; this includes the detection of deep-water predatory king crabs whose potential shoreward expansion to warming shelves has sparked much concern. Using a customized bioinformatics pipeline, we identified abundant signatures of common benthic invertebrate fauna, endemic notothenioid fishes, as well as lithodid king crabs. We also uncovered species richness and diversity comparable to biological inventories compiled by the use of traditional survey methods, supporting the efficacy of the eDNA shotgun sequencing approach. As the rate of eDNA degradation affects faunal detection sensitivity, we also quantified mitochondrial ND2 gene copies in eDNA derived from a WAP icefish and found ND2 copies persisted to at least 20 days in the cold WAP water, much longer than values reported for temperate environments. We propose that eDNA metagenomic sequencing complements traditional sampling, and combining both will enable more inclusive biodiversity detection and faunal change monitoring in the vast Southern Ocean.
机译:西南南极半岛(WAP)是南极洲最快的变暖区,其中对冷适应海洋生态系统的气候影响已经可见。为了监测远程南极水域的远程庞大机构的群体变化,有效和信息化工具至关重要。环境DNA(EDNA)的高通量排序已成为监测生物多样性和生态系统的一种这样的工具,因为它增加了分类群的检测灵敏度,并且采样往往比传统的收集方法更简单,更昂贵且昂贵。我们从四个WAP浅(<= 300米)的架子区域收集水样,在其中恢复edna,并进行了偏见的霰弹枪测序和分析,以确定该方法评估海洋底栖动物群多样性的有效性;这包括检测深水掠食性王蟹,其潜在的普通扩张对变暖架的膨胀已经引发了很多问题。使用定制的生物信息学管道,我们确定了普通底栖无脊椎动物动物的丰富签名,流行的Notheniaid鱼类,以及Lithodid王蟹。我们还发现了与使用传统调查方法编制的生物库存相当的物种丰富性和多样性,支持EDNA霰弹枪测序方法的功效。随着EDNA降解的速率影响群体检测灵敏度,我们还定量了衍生自WAP冰鱼的EDNA中的线粒体ND2基因拷贝,发现ND2拷贝持续到冷WAP水中至少20天,比报告的温带环境的值长。我们提出EDNA Metagenomic测序补充了传统的采样,并结合两者将在广阔的南洋中实现更多包容性生物多样性检测和鳄碍变革监测。

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