基于edna的爱沙尼亚小龙虾入侵和小龙虾鼠疫检测

Q1 Agricultural and Biological Sciences
Michael Oliewo Aluma, Katrin Kaldre, David A. Strand, Margo Hurt, Lilian Pukk
{"title":"基于edna的爱沙尼亚小龙虾入侵和小龙虾鼠疫检测","authors":"Michael Oliewo Aluma,&nbsp;Katrin Kaldre,&nbsp;David A. Strand,&nbsp;Margo Hurt,&nbsp;Lilian Pukk","doi":"10.1002/edn3.70107","DOIUrl":null,"url":null,"abstract":"<p>In Estonia, three invasive North American crayfish species—<i>Pacifastacus leniusculus</i>, <i>Faxonius limosus</i>, and <i>Procambarus virginalis</i>—have been detected through the annual monitoring program. To protect <i>Astacus astacus</i>, the only native freshwater crayfish species in Estonia, rapid and effective conservation-based management actions are necessary. Recently, the environmental DNA (eDNA) approach has been increasingly used in Europe to detect crayfish species and the crayfish plague pathogen <i>Aphanomyces astaci</i>. Our study explored the potential of integrating the eDNA approach into ongoing annual monitoring programs for invasive crayfish species and <i>A. astaci</i>. We also evaluated the relationship between eDNA concentration and signal crayfish population density at a single location. We filtered 139 eDNA samples from 16 water bodies and screened them for <i>A. astacus</i>, <i>P. leniusculus</i>, and <i>A. astaci</i> using singleplex qPCR assays. A subset of the samples was also screened for <i>P. virginalis</i> and <i>F. limosus</i>. Crayfish eDNA was detected in nine out of 14 water bodies where presence was confirmed by trapping, resulting in a 64% detection efficiency. Detection of <i>P. virginalis</i> was only observed in samples with amplifications below the limit of detection, and <i>A. astaci</i> eDNA was found in only one water body hosting invasive crayfish species. Although we could not establish a convincing quantitative correlation between the estimated <i>P. leniusculus</i> eDNA concentration and crayfish population density, we conclude that the eDNA approach is promising and, with further optimization, it can be integrated into routine monitoring of crayfish and crayfish plague pathogen as a supplement to traditional trapping methods.</p>","PeriodicalId":52828,"journal":{"name":"Environmental DNA","volume":"7 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/edn3.70107","citationCount":"0","resultStr":"{\"title\":\"eDNA-Based Detection of Invasive Crayfish and Crayfish Plague in Estonia\",\"authors\":\"Michael Oliewo Aluma,&nbsp;Katrin Kaldre,&nbsp;David A. Strand,&nbsp;Margo Hurt,&nbsp;Lilian Pukk\",\"doi\":\"10.1002/edn3.70107\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In Estonia, three invasive North American crayfish species—<i>Pacifastacus leniusculus</i>, <i>Faxonius limosus</i>, and <i>Procambarus virginalis</i>—have been detected through the annual monitoring program. To protect <i>Astacus astacus</i>, the only native freshwater crayfish species in Estonia, rapid and effective conservation-based management actions are necessary. Recently, the environmental DNA (eDNA) approach has been increasingly used in Europe to detect crayfish species and the crayfish plague pathogen <i>Aphanomyces astaci</i>. Our study explored the potential of integrating the eDNA approach into ongoing annual monitoring programs for invasive crayfish species and <i>A. astaci</i>. We also evaluated the relationship between eDNA concentration and signal crayfish population density at a single location. We filtered 139 eDNA samples from 16 water bodies and screened them for <i>A. astacus</i>, <i>P. leniusculus</i>, and <i>A. astaci</i> using singleplex qPCR assays. A subset of the samples was also screened for <i>P. virginalis</i> and <i>F. limosus</i>. Crayfish eDNA was detected in nine out of 14 water bodies where presence was confirmed by trapping, resulting in a 64% detection efficiency. Detection of <i>P. virginalis</i> was only observed in samples with amplifications below the limit of detection, and <i>A. astaci</i> eDNA was found in only one water body hosting invasive crayfish species. Although we could not establish a convincing quantitative correlation between the estimated <i>P. leniusculus</i> eDNA concentration and crayfish population density, we conclude that the eDNA approach is promising and, with further optimization, it can be integrated into routine monitoring of crayfish and crayfish plague pathogen as a supplement to traditional trapping methods.</p>\",\"PeriodicalId\":52828,\"journal\":{\"name\":\"Environmental DNA\",\"volume\":\"7 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/edn3.70107\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental DNA\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/edn3.70107\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Agricultural and Biological Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental DNA","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/edn3.70107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0

摘要

在爱沙尼亚,通过年度监测项目,已经发现了三种入侵的北美小龙虾——太平洋螯虾、狐尾螯虾和弗吉尼亚原螯虾。为了保护Astacus Astacus,爱沙尼亚唯一的本地淡水小龙虾物种,必须采取快速有效的保护管理措施。近年来,环境DNA (environmental DNA, eDNA)检测方法在欧洲越来越多地应用于小龙虾种类和小龙虾鼠疫病原菌的检测。我们的研究探索了将eDNA方法整合到正在进行的入侵小龙虾物种和亚洲螯虾的年度监测计划中的潜力。我们还评估了eDNA浓度与单个地点信号小龙虾种群密度之间的关系。我们从16个水体中筛选了139份eDNA样本,并使用单链qPCR技术对astacus、P. leniusculus和astaci进行了筛选。对部分样品也进行了处女假单胞菌和腐毛假单胞菌的筛选。在捕获确认存在的14个水体中,有9个水体检测到小龙虾eDNA,检测效率为64%。仅在扩增量低于检测限的样品中检测到f . virginalis,仅在一个携带入侵小龙虾的水体中检测到A. astaci的eDNA。虽然我们还不能确定小龙虾种群密度与小龙虾eDNA浓度之间的定量相关性,但我们认为eDNA方法是有前景的,并且在进一步优化的情况下,它可以作为传统捕获方法的补充,整合到小龙虾和小龙虾鼠疫病原体的常规监测中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
eDNA-Based Detection of Invasive Crayfish and Crayfish Plague in Estonia

In Estonia, three invasive North American crayfish species—Pacifastacus leniusculus, Faxonius limosus, and Procambarus virginalis—have been detected through the annual monitoring program. To protect Astacus astacus, the only native freshwater crayfish species in Estonia, rapid and effective conservation-based management actions are necessary. Recently, the environmental DNA (eDNA) approach has been increasingly used in Europe to detect crayfish species and the crayfish plague pathogen Aphanomyces astaci. Our study explored the potential of integrating the eDNA approach into ongoing annual monitoring programs for invasive crayfish species and A. astaci. We also evaluated the relationship between eDNA concentration and signal crayfish population density at a single location. We filtered 139 eDNA samples from 16 water bodies and screened them for A. astacus, P. leniusculus, and A. astaci using singleplex qPCR assays. A subset of the samples was also screened for P. virginalis and F. limosus. Crayfish eDNA was detected in nine out of 14 water bodies where presence was confirmed by trapping, resulting in a 64% detection efficiency. Detection of P. virginalis was only observed in samples with amplifications below the limit of detection, and A. astaci eDNA was found in only one water body hosting invasive crayfish species. Although we could not establish a convincing quantitative correlation between the estimated P. leniusculus eDNA concentration and crayfish population density, we conclude that the eDNA approach is promising and, with further optimization, it can be integrated into routine monitoring of crayfish and crayfish plague pathogen as a supplement to traditional trapping methods.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Environmental DNA
Environmental DNA Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
11.00
自引率
0.00%
发文量
99
审稿时长
16 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信