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一种利用 eDNA-qPCR 技术检测寄生虫在其三刺鱼宿主体内存在情况的方法。

An eDNA-qPCR assay to detect the presence of the parasite inside its threespine stickleback host.

机构信息

Département de Biologie et Institut de Biologie Intégrative et des Systèmes (IBIS), Université Laval, Québec, QC, Canada G1V 0A6.

Département de Biologie et Institut de Biologie Intégrative et des Systèmes (IBIS), Université Laval, Québec, QC, Canada G1V 0A6

出版信息

J Exp Biol. 2018 May 10;221(Pt 9):jeb178137. doi: 10.1242/jeb.178137.

Abstract

Detecting the presence of a parasite within its host is crucial to the study of host-parasite interactions. The -threespine stickleback pair has been studied extensively to investigate host phenotypic alterations associated with a parasite with a complex life cycle. This cestode is localized inside the stickleback's abdominal cavity and can be visually detected only once it passes a mass threshold. We present a non-lethal quantitative PCR (qPCR) approach based on detection of environmental DNA from the worm (eDNA), sampled in the fish abdominal cavity. Using this approach on two fish populations (=151), 98% of fish were correctly assigned to their infection status. There was a significant correlation between eDNA concentration and total parasitic mass. We also assessed ventilation rate as a complementary mean to detect infection. Our eDNA detection method gives a reliable presence/absence response and its future use for quantitative assessment of infection is promising.

摘要

检测寄生虫在宿主中的存在对于研究宿主-寄生虫相互作用至关重要。三刺鱼对已经被广泛研究,以调查与具有复杂生命周期的寄生虫相关的宿主表型改变。这种绦虫位于刺鱼的腹腔内,只有当它超过一定质量阈值时才能被肉眼检测到。我们提出了一种非致死性的定量 PCR(qPCR)方法,基于从鱼腹腔中取样的蠕虫(eDNA)的检测。使用这种方法对两个鱼类种群(=151)进行分析,98%的鱼被正确分配到它们的感染状态。eDNA 浓度与总寄生质量之间存在显著相关性。我们还评估了通风率作为一种补充手段来检测感染。我们的 eDNA 检测方法给出了可靠的存在/缺失反应,其未来用于定量评估感染具有很大的潜力。

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