Nayak Debi P, Balogun Rilwan A, Yamada Hiroshi, Zhou Z Hong, Barman Subrata
Department of Microbiology, Immunology and Molecular Genetics, Molecular Biology Institute, Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Virus Res. 2009 Aug;143(2):147-61. doi: 10.1016/j.virusres.2009.05.010. Epub 2009 May 27.
Influenza viruses are enveloped, negative stranded, segmented RNA viruses belonging to Orthomyxoviridae family. Each virion consists of three major sub-viral components, namely (i) a viral envelope decorated with three transmembrane proteins hemagglutinin (HA), neuraminidase (NA) and M2, (ii) an intermediate layer of matrix protein (M1), and (iii) an innermost helical viral ribonucleocapsid [vRNP] core formed by nucleoprotein (NP) and negative strand viral RNA (vRNA). Since complete virus particles are not found inside the cell, the processes of assembly, morphogenesis, budding and release of progeny virus particles at the plasma membrane of the infected cells are critically important for the production of infectious virions and pathogenesis of influenza viruses as well. Morphogenesis and budding require that all virus components must be brought to the budding site which is the apical plasma membrane in polarized epithelial cells whether in vitro cultured cells or in vivo infected animals. HA and NA forming the outer spikes on the viral envelope possess apical sorting signals and use exocytic pathways and lipid rafts for cell surface transport and apical sorting. NP also has apical determinant(s) and is probably transported to the apical budding site similarly via lipid rafts and/or through cortical actin microfilaments. M1 binds the NP and the exposed RNAs of vRNPs, as well as to the cytoplasmic tails (CT) and transmembrane (TM) domains of HA, NA and M2, and is likely brought to the budding site on the piggy-back of vRNP and transmembrane proteins. Budding processes involve bud initiation, bud growth and bud release. The presence of lipid rafts and assembly of viral components at the budding site can cause asymmetry of lipid bilayers and outward membrane bending leading to bud initiation and bud growth. Bud release requires fusion of the apposing viral and cellular membranes and scission of the virus buds from the infected cellular membrane. The processes involved in bud initiation, bud growth and bud scission/release require involvement both viral and host components and can affect bud closing and virus release in both positive and negative ways. Among the viral components, M1, M2 and NA play important roles in bud release and M1, M2 and NA mutations all affect the morphology of buds and released viruses. Disassembly of host cortical actin microfilaments at the pinching-off site appears to facilitate bud fission and release. Bud scission is energy dependent and only a small fraction of virus buds present on the cell surface is released. Discontinuity of M1 layer underneath the lipid bilayer, absence of outer membrane spikes, absence of lipid rafts in the lipid bilayer, as well as possible presence of M2 and disassembly of cortical actin microfilaments at the pinching-off site appear to facilitate bud fission and bud release. We provide our current understanding of these important processes leading to the production of infectious influenza virus particles.
流感病毒是包膜的、负链的、分节段的RNA病毒,属于正粘病毒科。每个病毒粒子由三个主要的亚病毒成分组成,即:(i)一个病毒包膜,其上装饰有三种跨膜蛋白血凝素(HA)、神经氨酸酶(NA)和M2;(ii)一层中间的基质蛋白(M1);(iii)最内层的螺旋形病毒核糖核蛋白[vRNP]核心,由核蛋白(NP)和负链病毒RNA(vRNA)形成。由于在细胞内未发现完整的病毒颗粒,子代病毒颗粒在被感染细胞的质膜上的组装、形态发生、出芽和释放过程对于感染性病毒粒子的产生以及流感病毒的发病机制也至关重要。形态发生和出芽要求所有病毒成分必须被带到出芽位点,在极化上皮细胞中该位点是顶端质膜,无论是体外培养的细胞还是体内感染的动物。形成病毒包膜上外部刺突的HA和NA具有顶端分选信号,并利用胞吐途径和脂筏进行细胞表面运输和顶端分选。NP也有顶端决定因素,可能通过脂筏和/或通过皮质肌动蛋白微丝类似地运输到顶端出芽位点。M1结合NP和vRNP的暴露RNA,以及HA、NA和M2的细胞质尾巴(CT)和跨膜(TM)结构域,并可能通过vRNP和跨膜蛋白搭载到出芽位点。出芽过程包括芽起始、芽生长和芽释放。脂筏的存在以及病毒成分在出芽位点的组装可导致脂质双层的不对称和向外的膜弯曲,从而导致芽起始和芽生长。芽释放需要相对的病毒膜和细胞膜融合,以及病毒芽从被感染的细胞膜上脱离。芽起始、芽生长和芽分裂/释放所涉及的过程需要病毒和宿主成分的参与,并且可以以正面和负面的方式影响芽闭合和病毒释放。在病毒成分中,M1、M2和NA在芽释放中起重要作用,M1、M2和NA的突变均影响芽和释放病毒的形态。宿主皮质肌动蛋白微丝在缢缩位点的解体似乎有助于芽分裂和释放。芽分裂是能量依赖的,并且细胞表面存在的病毒芽只有一小部分被释放。脂质双层下方M1层的不连续性、外膜刺突的缺失、脂质双层中脂筏的缺失,以及在缢缩位点可能存在的M2和皮质肌动蛋白微丝的解体似乎有助于芽分裂和芽释放。我们阐述了目前对这些导致感染性流感病毒粒子产生的重要过程的理解。