Centre for Research in Therapeutic Solutions, Biomedical Sciences, Faculty of Science and Technology, University of Canberra, Canberra, ACT, Australia.
Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Methods Mol Biol. 2024;2837:125-135. doi: 10.1007/978-1-0716-4027-2_11.
Hepatitis B virus (HBV) is undoubtedly a master in exploiting host resources while evading host defense for its multiplication within a constrained genetic coding capacity. To further unravel these cunning strategies, a clear picture of virus-host interaction with key subcellular and molecular contexts is needed. Here, we describe a FISH protocol modified from the ViewRNA assay that allows direct visualization of HBV RNA, DNA, and cccDNA in cell culture models (e.g., HepAD38, HepG2-NTCP). It can be coupled with immunofluorescence staining of viral or host proteins or other fluorescent tagging systems which could illuminate numerous aspects of virus-host interactions.
乙型肝炎病毒(HBV)无疑是在有限的遗传编码能力内增殖的过程中利用宿主资源并逃避宿主防御的大师。为了进一步揭示这些狡猾的策略,需要清楚地了解病毒-宿主相互作用与关键的亚细胞和分子环境。在这里,我们描述了一种从 ViewRNA 检测法修改而来的 FISH 方案,该方案允许在细胞培养模型(例如 HepAD38、HepG2-NTCP)中直接可视化 HBV RNA、DNA 和 cccDNA。它可以与病毒或宿主蛋白的免疫荧光染色或其他荧光标记系统结合使用,从而可以阐明病毒-宿主相互作用的许多方面。