Scanning amplicons with CRISPR-Dx detects endangered amphibians in environmental DNA

IF 5.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Resources Pub Date : 2024-08-16 DOI:10.1111/1755-0998.14009
Flurin Leugger, Michel Schmidlin, Martina Lüthi, Zacharias Kontarakis, Loïc Pellissier
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Abstract

More efficient methods for extensive biodiversity monitoring are required to support rapid measures to address the biodiversity crisis. While environmental DNA (eDNA) metabarcoding and quantitative PCR (qPCR) methods offer advantages over traditional monitoring approaches, their large-scale application is limited by the time and labour required for developing assays and/or for analysis. CRISPR (clustered regularly interspaced short palindromic repeats) diagnostic technologies (Dx) may overcome some of these limitations, but they have been used solely with species-specific primers, restricting their versatility for biodiversity monitoring. Here, we demonstrate the feasibility of designing species-specific CRISPR-Dx assays in silico within a short metabarcoding fragment using a general primer set, a methodology we term ‘ampliscanning’, for 18 of the 22 amphibian species in Switzerland. We sub-selected nine species, including three classified as regionally endangered, to test the methodology using eDNA sampled from ponds at nine sites. We compared the ampliscanning detections to data from traditional monitoring at these sites. Ampliscanning was successful at detecting target species with different prevalences across the landscape. With only one visit, we detected more species per site than three traditional monitoring visits (visual and acoustic detections by trained experts), in particular more elusive species and previously undocumented but expected populations. Ampliscanning detected 25 species/site combinations compared to 12 with traditional monitoring. Sensitivity analyses showed that larger numbers of field visits and PCR replicates are more important for reliable detection than many technical replicates at the CRISPR-Dx assay level. Given the reduced sampling and analysis effort, our results highlight the benefits of eDNA and CRISPR-Dx combined with universal primers for large-scale monitoring of multiple endangered species across landscapes to inform conservation measures.

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利用 CRISPR-Dx 扫描扩增子,检测环境 DNA 中的濒危两栖动物。
需要更有效的方法来广泛监测生物多样性,以支持快速采取措施应对生物多样性危机。与传统监测方法相比,环境 DNA(eDNA)元条码和定量 PCR(qPCR)方法具有优势,但其大规模应用受到开发检测方法和/或进行分析所需的时间和劳动力的限制。CRISPR(聚类有规则间隔短回文重复序列)诊断技术(Dx)可以克服其中的一些局限性,但它们一直只用于物种特异性引物,限制了其在生物多样性监测方面的通用性。在这里,我们针对瑞士 22 个两栖动物物种中的 18 个物种,利用通用引物集在短元条码片段内设计物种特异性 CRISPR-Dx 检测方法(我们称之为 "扩增扫描")的可行性进行了演示。我们从九个地点的池塘中抽取了 eDNA 样本,对九个物种(包括三个被列为地区濒危物种)进行了子选择,以测试该方法。我们将扩增扫描检测结果与这些地点的传统监测数据进行了比较。扩增扫描成功地检测到了整个地貌中不同流行率的目标物种。与传统的三次监测(由经过培训的专家进行视觉和声学检测)相比,我们仅用一次访问就能在每个地点检测到更多物种,尤其是更难以捉摸的物种和以前未记录但预期的种群。放大扫描发现了 25 个物种/地点组合,而传统监测只发现了 12 个。敏感性分析表明,在 CRISPR-Dx 检测水平上,更多的实地考察和 PCR 重复比许多技术重复对可靠检测更为重要。由于减少了取样和分析工作,我们的结果凸显了 eDNA 和 CRISPR-Dx 与通用引物相结合的优势,可用于大规模监测跨地貌的多种濒危物种,为保护措施提供信息。
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来源期刊
Molecular Ecology Resources
Molecular Ecology Resources 生物-进化生物学
CiteScore
15.60
自引率
5.20%
发文量
170
审稿时长
3 months
期刊介绍: Molecular Ecology Resources promotes the creation of comprehensive resources for the scientific community, encompassing computer programs, statistical and molecular advancements, and a diverse array of molecular tools. Serving as a conduit for disseminating these resources, the journal targets a broad audience of researchers in the fields of evolution, ecology, and conservation. Articles in Molecular Ecology Resources are crafted to support investigations tackling significant questions within these disciplines. In addition to original resource articles, Molecular Ecology Resources features Reviews, Opinions, and Comments relevant to the field. The journal also periodically releases Special Issues focusing on resource development within specific areas.
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