Organtini Lindsey J, Shingler Kristin L, Ashley Robert E, Capaldi Elizabeth A, Durrani Kulsoom, Dryden Kelly A, Makhov Alexander M, Conway James F, Pizzorno Marie C, Hafenstein Susan
Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
Bucknell University, Lewisburg, Pennsylvania, USA.
J Virol. 2017 Jan 3;91(2). doi: 10.1128/JVI.01795-16. Print 2017 Jan 15.
The picornavirus-like deformed wing virus (DWV) has been directly linked to colony collapse; however, little is known about the mechanisms of host attachment or entry for DWV or its molecular and structural details. Here we report the three-dimensional (3-D) structures of DWV capsids isolated from infected honey bees, including the immature procapsid, the genome-filled virion, the putative entry intermediate (A-particle), and the empty capsid that remains after genome release. The capsids are decorated by large spikes around the 5-fold vertices. The 5-fold spikes had an open flower-like conformation for the procapsid and genome-filled capsids, whereas the putative A-particle and empty capsids that had released the genome had a closed tube-like spike conformation. Between the two conformations, the spikes undergo a significant hinge-like movement that we predicted using a Robetta model of the structure comprising the spike. We conclude that the spike structures likely serve a function during host entry, changing conformation to release the genome, and that the genome may escape from a 5-fold vertex to initiate infection. Finally, the structures illustrate that, similarly to picornaviruses, DWV forms alternate particle conformations implicated in assembly, host attachment, and RNA release.
Honey bees are critical for global agriculture, but dramatic losses of entire hives have been reported in numerous countries since 2006. Deformed wing virus (DWV) and infestation with the ectoparasitic mite Varroa destructor have been linked to colony collapse disorder. DWV was purified from infected adult worker bees to pursue biochemical and structural studies that allowed the first glimpse into the conformational changes that may be required during transmission and genome release for DWV.
类微小核糖核酸病毒的翅变形病毒(DWV)已被直接关联到蜂群崩溃;然而,对于DWV的宿主附着或进入机制及其分子和结构细节知之甚少。在此,我们报告了从受感染蜜蜂中分离出的DWV衣壳的三维(3-D)结构,包括未成熟的原衣壳、基因组填充的病毒粒子、假定的进入中间体(A粒子)以及基因组释放后残留的空衣壳。衣壳在五重顶点周围由大的刺突修饰。五重刺突对于原衣壳和基因组填充的衣壳具有开放的花状构象,而已经释放基因组的假定A粒子和空衣壳具有封闭的管状刺突构象。在这两种构象之间,刺突经历了显著的类似铰链的运动,我们使用包含刺突的结构的Robetta模型对此进行了预测。我们得出结论,刺突结构可能在宿主进入过程中发挥作用,改变构象以释放基因组,并且基因组可能从五重顶点逸出以引发感染。最后,这些结构表明,与微小核糖核酸病毒类似,DWV形成了与组装、宿主附着和RNA释放有关的交替粒子构象。
蜜蜂对全球农业至关重要,但自2006年以来,许多国家都报告了整个蜂群的大量损失。翅变形病毒(DWV)和外寄生螨瓦螨的侵扰与蜂群崩溃失调有关。从受感染的成年工蜂中纯化出DWV,以进行生化和结构研究,从而首次深入了解DWV在传播和基因组释放过程中可能需要的构象变化。