Department of Virology & Molecular Biology, Wageningen Bioveterinary Research, Lelystad, The Netherlands.
Laboratory of Virology, Wageningen University & Research, Wageningen, The Netherlands.
Methods Mol Biol. 2024;2824:347-360. doi: 10.1007/978-1-0716-3926-9_21.
The genome of most bunyaviruses is divided over three (S, M, and L) single-stranded RNA segments of negative polarity. The three viral RNA segments are essential to establish a productive infection. RNA fluorescence in situ hybridization (FISH) enables the detection, localization, and quantification of RNA molecules at single-molecule resolution. This chapter describes an RNA FISH method to directly visualize individual segment-specific bunyavirus RNAs in fixed infected cells and in mature virus particles, using Rift Valley fever virus as an example. Imaging of bunyavirus RNA segments is a valuable experimental tool to investigate fundamental aspects of the bunyavirus life cycle, such as virus replication, genome packaging, and virion assembly, among others.
大多数布尼亚病毒的基因组由三个(S、M 和 L)单链负义 RNA 片段组成。这三个病毒 RNA 片段对于建立有效的感染是必不可少的。RNA 荧光原位杂交(FISH)能够以单分子分辨率检测、定位和定量 RNA 分子。本章以裂谷热病毒为例,描述了一种直接可视化固定感染细胞和成熟病毒颗粒中单个节段特异性布尼亚病毒 RNA 的 RNA FISH 方法。布尼亚病毒 RNA 片段的成像是研究布尼亚病毒生命周期基本方面的一种有价值的实验工具,例如病毒复制、基因组包装和病毒粒子组装等。