Department of Veterinary and Biomedical Sciences, the Pennsylvania State University, 115 Henning Building, University Park, PA 16802, USA.
J Virol. 2010 Dec;84(24):12810-23. doi: 10.1128/JVI.01885-10. Epub 2010 Oct 13.
Enveloped virus particles are formed by budding from infected-cell membranes. For paramyxoviruses, viral matrix (M) proteins are key drivers of virus assembly and budding. However, other paramyxovirus proteins, including glycoproteins, nucleocapsid (NP or N) proteins, and C proteins, are also important for particle formation in some cases. To investigate the role of NP protein in parainfluenza virus 5 (PIV5) particle formation, NP protein truncation and substitution mutants were analyzed. Alterations near the C-terminal end of NP protein completely disrupted its virus-like particle (VLP) production function and significantly impaired M-NP protein interaction. Recombinant viruses with altered NP proteins were generated, and these viruses acquired second-site mutations. Recombinant viruses propagated in Vero cells acquired mutations that mainly affected components of the viral polymerase, while recombinant viruses propagated in MDBK cells acquired mutations that mainly affected the viral M protein. Two of the Vero-propagated viruses acquired the same mutation, V/P(S157F), found previously to be responsible for elevated viral gene expression induced by a well-characterized variant of PIV5, P/V-CPI(-). Vero-propagated viruses caused elevated viral protein synthesis and spread rapidly through infected monolayers by direct cell-cell fusion, bypassing the need to bud infectious virions. Both Vero- and MDBK-propagated viruses exhibited infectivity defects and altered polypeptide composition, consistent with poor incorporation of viral ribonucleoprotein complexes (RNPs) into budding virions. Second-site mutations affecting M protein restored interaction with altered NP proteins in some cases and improved VLP production. These results suggest that multiple avenues are available to paramyxoviruses for overcoming defects in M-NP protein interaction.
包膜病毒颗粒通过从感染细胞的细胞膜出芽形成。对于副粘病毒而言,病毒基质 (M) 蛋白是病毒组装和出芽的关键驱动因素。然而,在某些情况下,其他副粘病毒蛋白,包括糖蛋白、核衣壳 (NP 或 N) 蛋白和 C 蛋白,对于颗粒形成也很重要。为了研究 NP 蛋白在副流感病毒 5 (PIV5) 颗粒形成中的作用,分析了 NP 蛋白的截断和取代突变体。NP 蛋白 C 端末端附近的改变完全破坏了其病毒样颗粒 (VLP) 产生功能,并显著削弱了 M-NP 蛋白相互作用。生成了具有改变的 NP 蛋白的重组病毒,这些病毒获得了第二位置突变。在 Vero 细胞中增殖的重组病毒获得了主要影响病毒聚合酶成分的突变,而在 MDBK 细胞中增殖的重组病毒获得了主要影响病毒 M 蛋白的突变。在 Vero 细胞中增殖的两种重组病毒获得了相同的突变,V/P(S157F),先前发现该突变负责由 PIV5 的一种特征明显的变体 P/V-CPI(-) 诱导的病毒基因表达的升高。Vero 细胞中增殖的病毒引起病毒蛋白合成的升高,并通过直接细胞-细胞融合迅速在受感染的单层中扩散,从而绕过了产生有感染力的病毒粒子的出芽过程。Vero 和 MDBK 细胞中增殖的病毒都表现出感染缺陷和改变的多肽组成,这与病毒核糖核蛋白复合物 (RNP) 难以掺入出芽病毒粒子一致。影响 M 蛋白的第二位置突变在某些情况下恢复了与改变的 NP 蛋白的相互作用,并改善了 VLP 的产生。这些结果表明,副粘病毒有多种途径可以克服 M-NP 蛋白相互作用的缺陷。