入侵中华绒螯蟹单种环境DNA qPCR检测方法的设计与验证

IF 6.2 Q1 Agricultural and Biological Sciences
Lauren S. J. Cook, Molly Ann Williams, David Bass, Paul F. Clark, David Morritt, Paul Stebbing, Andrew G. Briscoe
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引用次数: 0

摘要

生物入侵是生物多样性丧失的主要驱动因素,并通过对当地生态系统的直接影响或通过修复和补救产生巨大的经济成本。减少入侵物种的影响是环境管理目标的一个关键方面,需要早期发现和全面的分布数据来进行有效的管理。环境DNA (eDNA)已被证明能够实现敏感的监测,能够在没有物理观察的情况下推断目标生物的存在,并且在入侵物种检测具有挑战性的水生环境中特别有利。中华绒螯蟹(Eriocheir sinensis)是世界上排名前100的入侵物种之一,被认为是全球最具破坏性的入侵物种之一,例如,通过通才捕食和作为小龙虾瘟疫的载体,对河岸、渔业和当地种群造成重大损害。在英国,人们对其分布仍然知之甚少,目前的管理依赖于报告特别的目击事件。本研究开发并验证了一种特异的qPCR检测方法,用于在标准化尺度上检测中华绒螯蟹的eDNA。引物设计利用在英国采集的中华按蚊及其近缘种的基因组扫描,最终检测限为15.6 copies/μL。在英国的实地测试中,尽管没有最近的视觉记录,但在三个有历史记录的地点发现了目标物种的eDNA。总的来说,该分析显示出作为一种支持环境监测的工具的潜力,并提供对中华依蚊分布、种群动态和入侵途径的见解,从而支持对中华依蚊的知情管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design and Validation of a Single-Species Environmental DNA qPCR Assay for the Detection of the Invasive Chinese Mitten Crab Eriocheir sinensis

Design and Validation of a Single-Species Environmental DNA qPCR Assay for the Detection of the Invasive Chinese Mitten Crab Eriocheir sinensis

Biological invasions are a leading driver of biodiversity loss and generate significant economic costs, either through direct impact on native ecosystems or through repairs and remediation. Reducing the impact of invasive species is a key aspect of environmental management targets, necessitating early detection and comprehensive distribution data for effective management. Environmental DNA (eDNA) has been demonstrated to enable sensitive monitoring, able to infer the presence of a target organism without physical observations and is particularly advantageous in aquatic environments where invasive species detection is challenging. The Chinese mitten crab (Eriocheir sinensis) is amongst the world's top 100 invasive species and is considered amongst the most damaging invasive species globally, causing significant detriment to riverbanks, fishing practices, and native populations, for example, through generalist predation and as a carrier of crayfish plague. In the UK, its distribution remains poorly understood, with current management relying on reporting of ad hoc sightings. This study developed and validated a species-specific qPCR assay for detecting E. sinensis eDNA against a standardized scale. Primer design utilized genome skimming of E. sinensis and related species collected in the UK, with the final assay achieving a detection limit of 15.6 copies/μL. Field tests in the UK detected target species eDNA at three sites with historical sightings, despite no recent visual records. Overall, the assay shows potential as a tool to support environmental monitoring and offer insights into the distribution, population dynamics, and invasion pathways, to support informed management of E. sinensis.

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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
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