Dai Wei, Jia Qingmei, Bortz Eric, Shah Sanket, Liu Jun, Atanasov Ivo, Li Xudong, Taylor Kenneth A, Sun Ren, Zhou Z Hong
Department of Pathology and Laboratory Medicine, University of Texas Medical School at Houston, Houston, TX 77030, USA.
J Struct Biol. 2008 Mar;161(3):428-38. doi: 10.1016/j.jsb.2007.10.010. Epub 2007 Nov 20.
Gammaherpesviruses, including the human pathogens Epstein-Barr virus and Kaposi's sarcoma-associated herpesvirus, are causative agents of lymphomas and other malignancies. The structural characterization of these viruses has been limited due to difficulties in obtaining adequate amount of virion particles. Here we report the first three-dimensional structural characterization of a whole gammaherpesvirus virion by an emerging integrated approach of cryo-electron tomography combined with single-particle cryo-electron microscopy, using murine gammaherpesvirus-68 (MHV-68) as a model system. We found that the MHV-68 virion consists of distinctive envelope and tegument compartments, and a highly conserved nucleocapsid. Two layers of tegument are identified: an inner tegument layer tethered to the underlying capsid and an outer, flexible tegument layer conforming to the overlying, pleomorphic envelope, consistent with the sequential viral tegumentation process inside host cells. Surprisingly, comparison of the MHV-68 virion and capsid reconstructions shows that the interactions between the capsid and inner tegument proteins are completely different from those observed in alpha and betaherpesviruses. These observations support the notion that the inner layer tegument across different subfamilies of herpesviruses has evolved significantly to confer specific characteristics related to viral-host interactions, in contrast to a highly conserved capsid for genome encapsidation and protection.
γ疱疹病毒,包括人类病原体爱泼斯坦-巴尔病毒和卡波西肉瘤相关疱疹病毒,是淋巴瘤和其他恶性肿瘤的病原体。由于难以获得足够数量的病毒粒子,这些病毒的结构特征一直受到限制。在这里,我们报告了通过一种新兴的冷冻电子断层扫描与单颗粒冷冻电子显微镜相结合的综合方法,对完整的γ疱疹病毒病毒粒子进行的首次三维结构表征,使用鼠γ疱疹病毒68(MHV-68)作为模型系统。我们发现,MHV-68病毒粒子由独特的包膜和被膜区室以及高度保守的核衣壳组成。鉴定出两层被膜:一层内层被膜与下面的衣壳相连,另一层外层灵活的被膜与上面的多形包膜相符合,这与宿主细胞内病毒被膜形成的顺序过程一致。令人惊讶的是,对MHV-68病毒粒子和衣壳重建的比较表明,衣壳与内层被膜蛋白之间的相互作用与在α和β疱疹病毒中观察到的完全不同。这些观察结果支持了这样一种观点,即与用于基因组包装和保护的高度保守的衣壳相比,疱疹病毒不同亚科的内层被膜已经发生了显著进化,以赋予与病毒-宿主相互作用相关的特定特征。