Taylor Matthew P, Kratchmarov Radomir, Enquist Lynn W
Department of Immunology and Infectious Diseases, Montana State University, USA.
J Vis Exp. 2013 Aug 16(78):50723. doi: 10.3791/50723.
Advances in live cell fluorescence microscopy techniques, as well as the construction of recombinant viral strains that express fluorescent fusion proteins have enabled real-time visualization of transport and spread of alphaherpes virus infection of neurons. The utility of novel fluorescent fusion proteins to viral membrane, tegument, and capsids, in conjunction with live cell imaging, identified viral particle assemblies undergoing transport within axons. Similar tools have been successfully employed for analyses of cell-cell spread of viral particles to quantify the number and diversity of virions transmitted between cells. Importantly, the techniques of live cell imaging of anterograde transport and spread produce a wealth of information including particle transport velocities, distributions of particles, and temporal analyses of protein localization. Alongside classical viral genetic techniques, these methodologies have provided critical insights into important mechanistic questions. In this article we describe in detail the imaging methods that were developed to answer basic questions of alphaherpes virus transport and spread.
活细胞荧光显微镜技术的进步,以及表达荧光融合蛋白的重组病毒株的构建,使得实时可视化甲型疱疹病毒感染神经元的运输和传播成为可能。新型荧光融合蛋白应用于病毒膜、被膜和衣壳,并结合活细胞成像,确定了在轴突内进行运输的病毒颗粒组装体。类似的工具已成功用于分析病毒颗粒的细胞间传播,以量化细胞间传播的病毒粒子数量和多样性。重要的是,顺行运输和传播的活细胞成像技术产生了大量信息,包括颗粒运输速度、颗粒分布以及蛋白质定位的时间分析。除了经典的病毒基因技术外,这些方法为重要的机制问题提供了关键见解。在本文中,我们详细描述了为回答甲型疱疹病毒运输和传播的基本问题而开发的成像方法。