Development, Validation, and Implementation of eDNA-Focused qPCR Assays to Detect and Distinguish Between Goldfish (Carassius auratus) and Prussian Carp (Carassius gibelio)

IF 6.2 Q1 Agricultural and Biological Sciences Environmental DNA Pub Date : 2025-04-05 DOI:10.1002/edn3.70092
Jacob R. Hambrook, Nicole Kimmel, Rick Robinson, Dean Foster, Mark Poesch, Patrick C. Hanington
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Abstract

The ability to accurately detect harmful aquatic invasive species in a species-specific manner is crucial to monitoring and management efforts. The Canadian province of Alberta currently harbors North America's only invasive Prussian Carp populations, in addition to invasive Goldfish populations. The ability to quickly and accurately distinguish between these phenotypically similar fish, while also determining their presence in various waterbodies, is important in tracking invasions. In this work, we develop a cytochrome B–based assay, as well as an ND2-based assay to distinguish between these two fish. The 84-bp-long CytB assay featured a limit of detection of 5.8 and 4.8 copies/sample for Prussian Carp and Goldfish, respectively, while the 95-bp-long ND2 assay featured LODs of 6.3 and 1.6 copies/sample, respectively. We demonstrate that each of these assays fails to amplify these markers in closely related fish species common to Alberta. They also fail to amplify key invasive carp species, apart from the Goldfish ND2 assay, which cross-reacts with Common Carp. We then implement these assays and find 13 Goldfish and 47 Prussian Carp environmental DNA detection events throughout the Canadian province of Alberta. Finally, we show that assays broadly agree with visual observation data gathered from various reporting mechanisms, highlighting their validity in a monitoring program.

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用于检测和区分金鱼(Carassius auratus)和普氏鲫(Carassius gibelio)的以 eDNA 为重点的 qPCR 分析的开发、验证和实施
以特定物种的方式准确检测有害水生入侵物种的能力对监测和管理工作至关重要。加拿大阿尔伯塔省目前拥有北美唯一的入侵普鲁士鲤鱼种群,以及入侵的金鱼种群。快速准确地区分这些表型相似的鱼类,同时确定它们在不同水体中的存在,对于追踪入侵非常重要。在这项工作中,我们开发了一种基于细胞色素b的检测方法,以及一种基于nd2的检测方法来区分这两种鱼。84 bp长的CytB检测方法对普鲁士鲤鱼和金鱼的检出限分别为5.8和4.8拷贝/份,而95 bp长的ND2检测方法的检出限分别为6.3和1.6拷贝/份。我们证明,这些分析中的每一个都不能在阿尔伯塔省常见的密切相关的鱼类中扩增这些标记。他们也不能扩增主要的入侵鲤鱼物种,除了金鱼ND2试验,它与普通鲤鱼发生交叉反应。然后,我们实施了这些检测,并在加拿大阿尔伯塔省发现了13条金鱼和47条普鲁士鲤鱼环境DNA检测事件。最后,我们表明分析与从各种报告机制收集的视觉观察数据大致一致,突出了它们在监测计划中的有效性。
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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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