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用于基于现场直接监测和实验室确认斑马贻贝属的环境DNA(eDNA)等温扩增

Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.

作者信息

Williams Maggie R, Stedtfeld Robert D, Engle Cathrine, Salach Paul, Fakher Umama, Stedtfeld Tiffany, Dreelin Erin, Stevenson R Jan, Latimore Jo, Hashsham Syed A

机构信息

Department of Civil and Environmental Engineering, Michigan State University, East Lansing, Michigan, United States of America.

Department of Fisheries and Wildlife, Michigan State University, East Lansing, Michigan, United States of America.

出版信息

PLoS One. 2017 Oct 16;12(10):e0186462. doi: 10.1371/journal.pone.0186462. eCollection 2017.

Abstract

Loop-mediated isothermal amplification (LAMP) of aquatic invasive species environmental DNA (AIS eDNA) was used for rapid, sensitive, and specific detection of Dreissena sp. relevant to the Great Lakes (USA) basin. The method was validated for two uses including i) direct amplification of eDNA using a hand filtration system and ii) confirmation of the results after DNA extraction using a conventional thermal cycler run at isothermal temperatures. Direct amplification eliminated the need for DNA extraction and purification and allowed detection of target invasive species in grab or concentrated surface water samples, containing both free DNA as well as larger cells and particulates, such as veligers, eggs, or seeds. The direct amplification method validation was conducted using Dreissena polymorpha and Dreissena bugensis and uses up to 1 L grab water samples for high target abundance (e.g., greater than 10 veligers (larval mussels) per L for Dreissena sp.) or 20 L samples concentrated through 35 μm nylon screens for low target abundance, at less than 10 veligers per liter water. Surface water concentrate samples were collected over a period of three years, mostly from inland lakes in Michigan with the help of a network of volunteers. Field samples collected from 318 surface water locations included i) filtered concentrate for direct amplification validation and ii) 1 L grab water sample for eDNA extraction and confirmation. Though the extraction-based protocol was more sensitive (resulting in more positive detections than direct amplification), direct amplification could be used for rapid screening, allowing for quicker action times. For samples collected between May and August, results of eDNA direct amplification were consistent with known presence/absence of selected invasive species. A cross-platform smartphone application was also developed to disseminate the analyzed results to volunteers. Field tests of the direct amplification protocol using a portable device (Gene-Z) showed the method could be used in the field to obtain results within one hr (from sample to result). Overall, the direct amplification has the potential to simplify the eDNA-based monitoring of multiple aquatic invasive species. Additional studies are warranted to establish quantitative correlation between eDNA copy number, veliger, biomass or organismal abundance in the field.

摘要

环介导等温扩增技术(LAMP)用于对水生入侵物种环境DNA(AIS eDNA)进行快速、灵敏且特异的检测,以检测与美国大湖流域相关的斑马贻贝属物种。该方法在两种应用中得到验证,包括:i)使用手动过滤系统直接扩增eDNA;ii)使用在等温温度下运行的传统热循环仪进行DNA提取后对结果进行确认。直接扩增无需进行DNA提取和纯化,可检测抓取或浓缩的地表水样本中的目标入侵物种,这些样本中既含有游离DNA,也含有较大的细胞和颗粒,如面盘幼虫、卵或种子。直接扩增方法的验证使用了多形斑马贻贝和锈色斑马贻贝,并针对高目标丰度(例如,每升水中斑马贻贝属物种的面盘幼虫(幼体贻贝)数量大于10个)使用多达1升的抓取水样,或针对低目标丰度(每升水中面盘幼虫数量少于10个)使用通过35μm尼龙筛网浓缩的20升样本。地表水浓缩样本在三年时间内收集,主要借助志愿者网络从密歇根州的内陆湖泊采集。从318个地表水地点采集的野外样本包括:i)用于直接扩增验证的过滤浓缩样本;ii)用于eDNA提取和确认的1升抓取水样。尽管基于提取的方案更灵敏(比直接扩增产生更多阳性检测结果),但直接扩增可用于快速筛查,从而缩短行动时间。对于5月至8月期间采集的样本,eDNA直接扩增结果与已知的选定入侵物种的存在/不存在情况一致。还开发了一款跨平台智能手机应用程序,将分析结果分发给志愿者。使用便携式设备(Gene-Z)对直接扩增方案进行的现场测试表明,该方法可在现场使用,1小时内(从样本到结果)获得结果。总体而言,直接扩增有潜力简化基于eDNA的多种水生入侵物种监测。有必要开展更多研究,以建立野外eDNA拷贝数、面盘幼虫、生物量或生物丰度之间的定量相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/318a/5643059/59e55ab1ff6e/pone.0186462.g001.jpg

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