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用于隐鳃鲵非侵入性环境DNA检测的线粒体高变区巢式PCR扩增

Nested PCR amplification of the mitochondrial hypervariable region for non-invasive eDNA detection of Cryptobranchus alleganiensis.

作者信息

Kurtz Patrick, Santo Domingo Jorge, Pyron Robert Alexander, Wendell David

机构信息

Department of Chemical and Environmental Engineering, University of Cincinnati, Cincinnati, Ohio, United States of America.

United States Environmental Protection Agency, Cincinnati, Ohio, United States of America.

出版信息

PLoS One. 2025 Jul 23;20(7):e0328633. doi: 10.1371/journal.pone.0328633. eCollection 2025.

DOI:10.1371/journal.pone.0328633
PMID:40700428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12286349/
Abstract

Environmental DNA (eDNA) has proven an invaluable tool in detecting elusive, endangered, or otherwise hard-to-identify species in aquatic ecosystems. The Eastern hellbender salamander (Cryptobranchus alleganiensis) is a fully aquatic amphibian with an increasingly threatened population due to its reliance on exceptional surface water with high levels of dissolved oxygen and low sediment. C. alleganiensis habitat and animal loss has been documented through conservation work, resulting in the U.S. Fish and Wildlife Service recently recommending C. alleganiensis as endangered under the Endangered Species Act. Recent natural disasters in population strongholds have emphasized the need for continued conservation efforts, including reliable, non-invasive methods for monitoring C. alleganiensis populations. Using eDNA extractions from environmental waters, we have developed a nested polymerase chain reaction (PCR) detection strategy targeting the control region of the C. alleganiensis mitochondrial genome. We demonstrate the efficacy of our nested primer set for the detection of Cryptobranchus salamanders in the Ohio River watershed with conventional PCR, quantitative PCR, and digital droplet PCR methods, and rigorously challenge these primers against diverse aquatic amphibian DNA templates found within their habitat using DNA sequencing to confirm the specificity of our target amplicons. Our nested PCR approach overcomes several shortcomings of previous eDNA detection methods for C. alleganiensis, most notably an order of magnitude improvement in the limit of detection for animal DNA in the field.

摘要

环境DNA(eDNA)已被证明是一种非常有价值的工具,可用于检测水生生态系统中难以捉摸、濒危或其他难以识别的物种。东部隐鳃鲵(Cryptobranchus alleganiensis)是一种完全水生的两栖动物,由于其依赖富含高溶解氧和低沉积物的优质地表水,其种群数量受到越来越大的威胁。通过保护工作已记录了隐鳃鲵的栖息地丧失和动物数量减少情况,这导致美国鱼类和野生动物管理局最近建议根据《濒危物种法》将隐鳃鲵列为濒危物种。其种群密集地区最近发生的自然灾害凸显了持续开展保护工作的必要性,包括采用可靠的非侵入性方法来监测隐鳃鲵种群。利用从环境水体中提取的eDNA,我们开发了一种针对隐鳃鲵线粒体基因组控制区的巢式聚合酶链反应(PCR)检测策略。我们用常规PCR、定量PCR和数字液滴PCR方法证明了我们的巢式引物组在俄亥俄河流域检测隐鳃鲵的有效性,并使用DNA测序对这些引物在其栖息地中发现的各种水生两栖动物DNA模板进行了严格验证,以确认我们目标扩增子的特异性。我们的巢式PCR方法克服了先前用于检测隐鳃鲵的eDNA检测方法的几个缺点,最显著的是在野外动物DNA检测限方面有一个数量级的提高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/b9f3895e1fc9/pone.0328633.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/7c8876a2972d/pone.0328633.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/11e1ee0f5885/pone.0328633.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/b9f3895e1fc9/pone.0328633.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/7c8876a2972d/pone.0328633.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/11e1ee0f5885/pone.0328633.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e34b/12286349/b9f3895e1fc9/pone.0328633.g003.jpg

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