Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, Davis, California, USA
Department of Pathology, College of Veterinary Medicine, University of Georgia, Athens, Athens, Georgia, USA.
J Virol. 2020 Jul 16;94(15). doi: 10.1128/JVI.00337-20.
The first isolation of a flavivirus from fish was made from moribund Chinook salmon () from the Eel River, California, USA. Following the observation of cytopathic effect in a striped-snakehead fish cell line, 35-nm virions with flaviviral morphology were visualized using electron microcopy. Next-generation sequencing and rapid amplification of cDNA ends obtained the complete genome. Reverse transcriptase quantitative PCR (RT-qPCR) confirmed the presence of viral RNA in formalin-fixed tissues from the wild salmon. For the first time, replication of an aquatic flavivirus was demonstrated following intracoelomic injection in a Chinook salmon model of infection. RT-qPCR demonstrated viral replication in salmon brains up to 15 days postinjection. Infectious virus was then reisolated in culture, fulfilling Rivers' postulates. Only limited replication occurred in the kidneys of Chinook salmon or in tissues of rainbow trout (). The proposed salmon flavivirus (SFV) has a 10.3-kb genome that encodes a rare dual open reading frame, a feature uncharacteristic of classical flaviviruses. Phylogenetic analysis places SFV in a basal position among a new subgroup of recently recognized aquatic and bat flaviviruses distinct from the established mosquito-borne, tick-borne, insect-only, and unknown-vector flavivirus groups. While the pathogenic potential of the virus remains to be fully elucidated, its basal phylogeny and the infection model will allow SFV to serve as a prototype for aquatic flaviviruses. Ongoing field and laboratory studies will facilitate better understanding of the potential impacts of SFV infection on ecologically and economically important salmonid species. Chinook salmon are a keystone fish species of great ecological and commercial significance in their native northern Pacific range and in regions to which they have been introduced. Threats to salmon populations include habitat degradation, climate change, and infectious agents, including viruses. While the first isolation of a flavivirus from wild migrating salmon may indicate an emerging disease threat, characterization of the genome provides insights into the ecology and long evolutionary history of this important group of viruses affecting humans and other animals and into an expanding group of recently discovered aquatic flaviviruses.
首次从鱼类中分离到黄病毒是在美国加利福尼亚州鳗鱼河濒死的奇努克鲑鱼()中发现的。在观察到条纹蛇头鱼细胞系中的细胞病变效应后,使用电子显微镜观察到具有黄病毒形态的 35nm 病毒粒子。下一代测序和快速 cDNA 末端扩增获得了完整的基因组。逆转录定量 PCR(RT-qPCR)证实了从野生鲑鱼的福尔马林固定组织中存在病毒 RNA。首次在奇努克鲑鱼感染模型中通过腹腔内注射证明了水生黄病毒的复制。RT-qPCR 证明了在注射后 15 天内鲑鱼脑中的病毒复制。然后在培养物中重新分离到感染性病毒,满足了里弗斯的假设。在奇努克鲑鱼的肾脏或虹鳟鱼()的组织中仅有限制性复制。该提议的鲑鱼黄病毒(SFV)具有 10.3kb 的基因组,编码一个罕见的双开放阅读框,这是经典黄病毒所没有的特征。系统发育分析将 SFV 置于最近发现的水生和蝙蝠黄病毒的一个新亚群的基础位置,与已确立的蚊媒、蜱媒、昆虫媒介和未知媒介黄病毒群不同。虽然该病毒的致病潜力仍有待充分阐明,但它的基础系统发育和感染模型将使 SFV 成为水生黄病毒的原型。正在进行的现场和实验室研究将有助于更好地了解 SFV 感染对生态和经济上重要的鲑鱼物种的潜在影响。奇努克鲑鱼是北太平洋原生范围和引入区域具有重要生态和商业意义的关键鱼类物种。对鲑鱼种群的威胁包括生境退化、气候变化以及包括病毒在内的传染性病原体。虽然从野生洄游鲑鱼中首次分离到黄病毒可能表明存在新出现的疾病威胁,但对基因组的特征描述提供了对影响人类和其他动物的这组重要病毒的生态和长期进化历史的深入了解,并提供了对最近发现的一组扩大的水生黄病毒的了解。