Jiang Ping, Liu Ying, Ma Hsin-Chieh, Paul Aniko V, Wimmer Eckard
Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York, USA.
Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York, USA
Microbiol Mol Biol Rev. 2014 Sep;78(3):418-37. doi: 10.1128/MMBR.00012-14.
The Picornaviridae represent a large family of small plus-strand RNA viruses that cause a bewildering array of important human and animal diseases. Morphogenesis is the least-understood step in the life cycle of these viruses, and this process is difficult to study because encapsidation is tightly coupled to genome translation and RNA replication. Although the basic steps of assembly have been known for some time, very few details are available about the mechanism and factors that regulate this process. Most of the information available has been derived from studies of enteroviruses, in particular poliovirus, where recent evidence has shown that, surprisingly, the specificity of encapsidation is governed by a viral protein-protein interaction that does not involve an RNA packaging signal. In this review, we make an attempt to summarize what is currently known about the following topics: (i) encapsidation intermediates, (ii) the specificity of encapsidation (iii), viral and cellular factors that are required for encapsidation, (iv) inhibitors of encapsidation, and (v) a model of enterovirus encapsidation. Finally, we compare some features of picornavirus morphogenesis with those of other plus-strand RNA viruses.
小核糖核酸病毒科是一个由小型正链RNA病毒组成的大家族,可引发一系列令人困惑的重要人类和动物疾病。形态发生是这些病毒生命周期中最不为人所理解的步骤,而且由于衣壳化与基因组翻译和RNA复制紧密耦合,这一过程很难研究。尽管组装的基本步骤已为人所知一段时间了,但关于调节这一过程的机制和因素的细节却非常少。现有的大部分信息来自肠道病毒的研究,特别是脊髓灰质炎病毒,最近的证据表明,令人惊讶的是,衣壳化的特异性由一种不涉及RNA包装信号的病毒蛋白-蛋白相互作用所控制。在这篇综述中,我们试图总结目前关于以下主题的已知信息:(i)衣壳化中间体,(ii)衣壳化的特异性,(iii)衣壳化所需的病毒和细胞因子,(iv)衣壳化抑制剂,以及(v)肠道病毒衣壳化模型。最后,我们比较了小核糖核酸病毒形态发生与其他正链RNA病毒的一些特征。