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一种用于检测入侵性铁锈蟹(Faxonius rusticus)的 eDNA 检测方法的更新和优化。

The update and optimization of an eDNA assay to detect the invasive rusty crayfish (Faxonius rusticus).

机构信息

Department of Biology, Randolph-Macon College, Ashland, Virginia, United States of America.

Department of Environmental Science, Fisheries and Aquatic Sciences Program, Juniata College, Huntingdon, Pennsylvania, United States of America.

出版信息

PLoS One. 2021 Oct 29;16(10):e0259084. doi: 10.1371/journal.pone.0259084. eCollection 2021.

Abstract

Environmental DNA (eDNA) is nuclear or mitochondrial DNA shed into the environment, and amplifying this DNA can serve as a reliable, noninvasive way to monitor aquatic systems for the presence of an invasive species. Assays based on the collection of eDNA are becoming increasingly popular, and, when optimized, can aid in effectively and efficiently tracking invasion fronts. We set out to update an eDNA assay to detect the invasive rusty crayfish, Faxonius rusticus. We tested for species specificity compared to other stream crayfish and field tested the assay at sites with known presence (N = 3) and absence (N = 4) in the Juniata River watershed in central Pennsylvania, USA. To maximize sensitivity, we field tested different storage buffers (Longmire's buffer and ethanol), DNA extraction methods (Qiagen's DNEasy and PowerWater kits), and quantitative polymerase chain reaction (qPCR) chemistries (TaqMan and SYBR green). Our assay confirmed the presence data and performed optimally when filter samples were stored in Longmire's buffer, DNA was extracted with DNeasy Blood and Tissue Kit, and TaqMan qPCR chemistry was utilized. With proper sample processing, our assay allows for accurate, noninvasive detection of F. rusticus in streams.

摘要

环境 DNA(eDNA)是指释放到环境中的核 DNA 或线粒体 DNA,扩增这些 DNA 可以作为一种可靠的、非侵入性的方法,用于监测水生系统中入侵物种的存在。基于 eDNA 收集的检测方法越来越受欢迎,并且经过优化后,可以有效地追踪入侵前沿。我们着手更新一种 eDNA 检测方法,以检测入侵性的铁锈小龙虾 Faxonius rusticus。我们测试了该方法与其他溪流小龙虾的物种特异性,并在美国宾夕法尼亚州中部 Juniata 河流域的已知存在(N = 3)和不存在(N = 4)地点进行了实地测试。为了最大限度地提高灵敏度,我们实地测试了不同的储存缓冲液(Longmire's buffer 和乙醇)、DNA 提取方法(Qiagen 的 DNEasy 和 PowerWater 试剂盒)和定量聚合酶链反应(qPCR)化学(TaqMan 和 SYBR green)。我们的检测方法证实了存在数据,并且在过滤样品储存在 Longmire's buffer 中、使用 DNeasy Blood and Tissue Kit 提取 DNA 以及使用 TaqMan qPCR 化学时表现最佳。通过适当的样品处理,我们的检测方法可以准确、非侵入性地检测溪流中的 F. rusticus。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8f9/8555798/c72cd3038d08/pone.0259084.g001.jpg

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