Department of Infectious Diseases, Yamagata University Faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata 990-9585, Japan.
J Virol. 2011 Feb;85(3):1322-9. doi: 10.1128/JVI.01367-10. Epub 2010 Nov 24.
CM2 is the second membrane protein of influenza C virus. Although its biochemical characteristics, coding strategy, and properties as an ion channel have been extensively studied, the role(s) of CM2 in the virus replication cycle remains to be clarified. In order to elucidate this role, in the present study we generated CM2-deficient influenza C virus-like particles (VLPs) and examined the VLP-producing 293T cells, VLPs, and VLP-infected HMV-II cells. Quantification of viral RNA (vRNA) in the VLPs by real-time PCR revealed that the CM2-deficient VLPs contain approximately one-third of the vRNA found in wild-type VLPs although no significant differences were detected in the expression levels of viral components in VLP-producing cells or in the number and morphology of the generated VLPs. This finding suggests that CM2 is involved in the genome packaging process into VLPs. Furthermore, HMV-II cells infected with CM2-deficient VLPs exhibited significantly reduced reporter gene expression. Although CM2-deficient VLPs could be internalized into HMV-II cells as efficiently as wild-type VLPs, a smaller amount of vRNA was detected in the nuclear fraction of CM2-deficient VLP-infected cells than in that of wild-type VLP-infected cells, suggesting that the uncoating process of the CM2-deficient VLPs in the infected cells did not proceed in an appropriate manner. Taken together, the data obtained in the present study indicate that CM2 has a potential role in the genome packaging and uncoating processes of the virus replication cycle.
CM2 是丙型流感病毒的第二种膜蛋白。尽管其生化特性、编码策略和作为离子通道的特性已得到广泛研究,但 CM2 在病毒复制周期中的作用仍有待阐明。为了阐明这一作用,本研究生成了 CM2 缺失的丙型流感病毒样颗粒(VLPs),并检测了产生 VLPs 的 293T 细胞、VLPs 和感染的 HMV-II 细胞。通过实时 PCR 对 VLPs 中的病毒 RNA(vRNA)进行定量,结果显示,CM2 缺失的 VLPs 中含有约三分之一的野生型 VLPs 中的 vRNA,尽管在产生 VLPs 的细胞中病毒成分的表达水平或产生的 VLPs 的数量和形态上没有检测到显著差异。这一发现表明 CM2 参与了基因组包装到 VLPs 的过程。此外,感染 CM2 缺失 VLPs 的 HMV-II 细胞表现出明显降低的报告基因表达。尽管 CM2 缺失的 VLPs 能够像野生型 VLPs 一样有效地被内化到 HMV-II 细胞中,但在 CM2 缺失的 VLP 感染细胞的核部分中检测到的 vRNA 量明显少于野生型 VLP 感染细胞,这表明感染细胞中 CM2 缺失的 VLPs 的脱壳过程没有以适当的方式进行。综上所述,本研究获得的数据表明,CM2 在病毒复制周期的基因组包装和脱壳过程中具有潜在作用。