Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Structure. 2010 Jan 13;18(1):47-58. doi: 10.1016/j.str.2009.10.017.
Gammaherpesviruses are etiologically associated with human tumors. A three-dimensional (3D) examination of their life cycle in the host is lacking, significantly limiting our understanding of the structural and molecular basis of virus-host interactions. Here, we report the first 3D visualization of key stages of the murine gammaherpesvirus 68 life cycle in NIH 3T3 cells, including viral attachment, entry, assembly, and egress, by dual-axis electron tomography. In particular, we revealed the transient processes of incoming capsids injecting viral DNA through nuclear pore complexes and nascent DNA being packaged into progeny capsids in vivo as a spool coaxial with the putative portal vertex. We discovered that intranuclear invagination of both nuclear membranes is involved in nuclear egress of herpesvirus capsids. Taken together, our results provide the structural basis for a detailed mechanistic description of gammaherpesvirus life cycle and also demonstrate the advantage of electron tomography in dissecting complex cellular processes of viral infection.
γ疱疹病毒与人类肿瘤在病因上有关联。宿主中其生命周期的三维(3D)检查仍然缺乏,这大大限制了我们对病毒-宿主相互作用的结构和分子基础的理解。在这里,我们通过双轴电子断层扫描报告了鼠γ疱疹病毒 68 生命周期的关键阶段的首次 3D 可视化,包括病毒附着、进入、组装和出芽,特别是我们揭示了传入衣壳通过核孔复合体注射病毒 DNA 的瞬时过程,以及新生 DNA 作为与假定门户顶点同轴的线轴被包装到子代衣壳中的过程。我们发现,核膜的核内内陷都参与了疱疹病毒衣壳的核出芽。总之,我们的结果为详细的γ疱疹病毒生命周期的机制描述提供了结构基础,同时也证明了电子断层扫描在剖析病毒感染的复杂细胞过程方面的优势。