Central Veterinary Institute of Wageningen UR (CVI), P.O. Box 65, Lelystad, The Netherlands.
J Virol. 2012 Nov;86(22):12341-50. doi: 10.1128/JVI.01725-12. Epub 2012 Sep 5.
Influenza viruses unable to express NS1 protein (delNS1) replicate poorly and induce large amounts of interferon (IFN). They are therefore considered candidate viruses for live-attenuated influenza vaccines. Their attenuated replication is generally assumed to result from the inability to counter the antiviral host response, as delNS1 viruses replicate efficiently in Vero cells, which lack IFN expression. In this study, delNS1 virus was parallel passaged on IFN-competent MDCK cells, which resulted in two strains that were able to replicate to high virus titers in MDCK cells due to adaptive mutations especially in the M-gene segment but also in the NP and NS gene segments. Most notable were clustered U-to-C mutations in the M segment of both strains and clustered A-to-G mutations in the NS segment of one strain, which presumably resulted from host cell-mediated RNA editing. The M segment mutations in both strains changed the ratio of M1 to M2 expression, probably by affecting splicing efficiency. In one virus, 2 amino acid substitutions in M1 additionally enhanced virus replication, possibly through changes in the M1 distribution between the nucleus and the cytoplasm. Both adapted viruses induced levels of IFN equal to that of the original delNS1 virus. These results show that the increased replication of the adapted viruses is not primarily due to altered IFN induction but rather is related to changes in M1 expression or localization. The mutations identified in this paper may be used to enhance delNS1 virus replication for vaccine production.
无法表达 NS1 蛋白的流感病毒(delNS1)复制能力较差,会诱导大量干扰素(IFN)。因此,它们被认为是活流感减毒疫苗的候选病毒。它们的复制能力减弱通常被认为是由于无法对抗抗病毒的宿主反应,因为 delNS1 病毒在缺乏 IFN 表达的 Vero 细胞中高效复制。在这项研究中,delNS1 病毒在具有 IFN 功能的 MDCK 细胞上平行传代,导致两种毒株由于适应性突变,特别是在 M 基因片段中,但也在 NP 和 NS 基因片段中,能够在 MDCK 细胞中复制到高病毒滴度。值得注意的是,两种毒株的 M 基因片段中都存在 U 到 C 的簇状突变,以及一种毒株 NS 基因片段中 A 到 G 的簇状突变,这可能是由于宿主细胞介导的 RNA 编辑所致。两种毒株的 M 片段突变改变了 M1 与 M2 的表达比例,可能通过影响剪接效率。在一种病毒中,M1 中的 2 个氨基酸取代进一步增强了病毒的复制能力,可能是通过改变 M1 在核和细胞质之间的分布。两种适应的病毒诱导的 IFN 水平与原始 delNS1 病毒相当。这些结果表明,适应病毒的复制增加不是主要由于 IFN 诱导的改变,而是与 M1 表达或定位的变化有关。本文鉴定的突变可能用于增强 delNS1 病毒的复制,以用于疫苗生产。