Biomedical Sciences Research Complex, University of St. Andrews, St. Andrews KY16 9ST, UK.
Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh EH16 4TJ, UK.
Viruses. 2020 May 12;12(5):532. doi: 10.3390/v12050532.
Environmental and agricultural pollination services by honey bees, , and honey production are compromised by high levels of annual colony losses globally. The majority are associated with disease caused by deformed wing virus (DWV), a positive-strand RNA virus, exacerbated by the ectoparasitic mite . To improve honey bee health, a better understanding of virus transmission and pathogenesis is needed which requires the development of tools to study virus replication, transmission, and localisation. We report the use of reverse genetic (RG) systems for the predominant genetically distinct variants of DWV to address these questions. All RG-recovered viruses replicate within 24 h post-inoculation of pupae and could recapitulate the characteristic symptoms of DWV disease upon eclosion. Larvae were significantly less susceptible but could be infected orally and subsequently developed disease. Using genetically tagged RG DWV and an feeding system, we demonstrate virus replication in the mite by accumulation of tagged negative-strand viral replication intermediates. We additionally apply a modified DWV genome expressing a fluorescent reporter protein for direct observation of virus distribution in injected pupae or fed larvae. Using this, we demonstrate extensive sites of virus replication in a range of pupal tissues and organs and in the nascent wing buds in larvae fed high levels of virus, indicative of a direct association between virus replication and pathogenesis. These studies provide insights into virus replication kinetics, tropism, transmission, and pathogenesis, and produce new tools to help develop the understanding needed to control DWV-mediated colony losses.
环境和农业传粉服务的蜜蜂、和蜂蜜生产受到全球年度蜂群损失水平高的影响。大多数与由变形翅膀病毒(DWV)引起的疾病有关,DWV 是一种正链 RNA 病毒,由外寄生虫螨加剧。为了改善蜜蜂健康,需要更好地了解病毒传播和发病机制,这需要开发研究病毒复制、传播和定位的工具。我们报告了使用反向遗传(RG)系统来研究主要的遗传上不同的 DWV 变体,以解决这些问题。所有 RG 恢复的病毒在接种蛹后 24 小时内复制,并且可以在羽化时再现 DWV 疾病的特征症状。幼虫的敏感性明显降低,但可以经口感染,并随后发展为疾病。使用遗传标记的 RG DWV 和喂食系统,我们证明了螨中病毒的复制,通过积累标记的负链病毒复制中间体。我们还应用了一种改良的 DWV 基因组,表达荧光报告蛋白,用于直接观察注射蛹或喂食幼虫中病毒的分布。使用这种方法,我们证明了在幼虫中,病毒在大量蛹组织和器官以及新生的翅膀芽中复制,这表明病毒复制与发病机制之间存在直接关联。这些研究提供了对病毒复制动力学、嗜性、传播和发病机制的深入了解,并产生了新的工具,有助于控制 DWV 介导的蜂群损失。