无火无烟:评价虹鳟鱼肠道红嘴病发病机制的拉克氏耶尔森菌水eDNA谱

Q1 Agricultural and Biological Sciences
Cyril Henard, Hanxi Li, Yajiao Duan, Moonika Marana, Per Kania, Kasper Villumsen, Barbara F. Nowak, Louise von Gersdorff Jørgensen
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引用次数: 0

摘要

在过去的几十年里,环境核酸(eDNA和eRNA)分析方法的应用迅速扩展到各个研究领域。最近,世界动物卫生组织提出了使用dna作为水产养殖疾病监测生物监测工具的准则。在虹鳟鱼实验诱发红口病的过程中,对拉克氏耶尔森菌的eDNA谱进行了监测。在死亡开始前和死亡开始后,将鱼的病原体负担、临床症状和免疫反应与水中病原体负担进行比较。研究人员使用了两种不同浓度的细菌进行感染,并评估了处理压力对鱼免疫反应的影响。在较高浓度的细菌中,在感染后3天(DPI),来自ruckeri的eDNA谱明显高于对照组,而在第一个采样点(1 DPI)报告了该疾病的第一个临床症状,优于eDNA谱。首次死亡记录在5 DPI。处理方案增加了感染较低浓度细菌的鱼的死亡率,但没有显著改变拉克氏耶氏菌的eDNA谱。在较高浓度的细菌中,eDNA谱与本研究研究的大多数免疫基因显著相关,它们主要参与炎症过程(il-6, il-8, il-10)和急性反应(saa, hep)。使用环境DNA是一种具有成本效益和非侵入性的水产养殖疾病风险生物监测方法。然而,这项研究强调了当鱼的免疫状态发生改变时,eDNA应用的局限性。在未来的感染实验中,应该研究eDNA和eRNA的联合方法,以评估来自宿主的eRNA是否可以提供有关免疫状态和死亡率增加风险的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

There is no Smoke Without Fire: Evaluation of Water eDNA Profile of Yersinia ruckeri to Assess Enteric Redmouth Disease Pathogenesis in Rainbow Trout (Oncorhynchus mykiss)

There is no Smoke Without Fire: Evaluation of Water eDNA Profile of Yersinia ruckeri to Assess Enteric Redmouth Disease Pathogenesis in Rainbow Trout (Oncorhynchus mykiss)

In the past couple of decades, applications of environmental nucleic acids (eDNA and eRNA) analysis methods have expanded rapidly into various research fields. Recently, the World Organisation for Animal Health presented guidelines for the use of eDNA as a biomonitoring tool for disease surveillance in aquaculture. In this paper, the eDNA profile of Yersinia ruckeri was monitored over the course of experimentally induced red mouth disease in rainbow trout. Before and after mortality started, the fish pathogen burden, clinical signs, and immune response were compared to the pathogen burden in the water. Two different concentrations of bacteria were used for the infection, and the effects of handling stress on the fish's immune response were evaluated. In the higher concentration of bacteria, the eDNA profiles from Y. ruckeri were significantly higher compared to control at 3 days post-infection (DPI) whereas the first clinical signs of the disease were reported at the first sampling point (1 DPI), outperforming the eDNA profiles. The first mortalities were recorded at 5 DPI. The handling protocol has increased mortality in fish infected with the lower concentration of bacteria without significant changes in the eDNA profile of Y. ruckeri. The eDNA profiles were significantly correlated with most of the immune genes investigated in this study in the higher concentration of bacteria, and they were primarily involved in the inflammation process (il-6, il-8, il-10) and acute response (saa, hep). The use of environmental DNA is a cost-effective and noninvasive approach for the biomonitoring of disease risks in aquaculture. Nevertheless, this study highlighted eDNA application limitations when the immune status of the fish is altered. A combined approach with eDNA and eRNA should be investigated in future infection experiments to evaluate if eRNA from the host could provide information about the immune status and the risk of increased mortality.

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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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