Odagiri T, Tobita K
Department of Virology, Jichi Medical School, Tochigi-ken, Japan.
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5988-92. doi: 10.1073/pnas.87.15.5988.
Several consecutive undiluted passages of infectious virus are usually required to obtain defective interfering particles of influenza virus. In contrast, a reassortant (Wa-182) of influenza A/WSN, which we isolated, whose NS gene was replaced with the NS gene of A/Aichi, was readily converted to defective interfering form after only a single high-multiplicity infection. The defective interfering particles of Wa-182 were devoid of the PA gene (RNA segment 3) but possessed several species of subgenomic RNAs of the PA gene origin. Such aberrant replication of the PA gene was shown to be caused by an extragenic effect of the NS gene of Wa-182, because, when the NS gene of Wa-182 was singly transferred to the wild-type A/Ann Arbor/6/60 virus, the recipient showed exactly the same features. Analysis of nucleotide sequence demonstrated that the NS gene of Wa-182 contained three point mutations relative to the wild-type NS gene that resulted in two amino acid substitutions in the nonstructural protein NS2, suggesting that the mutation in NS2 protein affected the normal replication of the PA gene of Wa-182. The results also suggest that the NS2 protein plays an important role in the synthesis of intact genome RNAs.
通常需要对感染性病毒进行几次连续的未稀释传代,才能获得流感病毒的缺陷干扰颗粒。相比之下,我们分离出的甲型流感病毒/WSN的重配体(Wa-182),其NS基因被A/爱知的NS基因取代,在仅进行一次高 multiplicity 感染后就很容易转化为缺陷干扰形式。Wa-182的缺陷干扰颗粒缺乏PA基因(RNA片段3),但拥有几种源自PA基因的亚基因组RNA。这种PA基因的异常复制被证明是由Wa-182的NS基因的基因外效应引起的,因为当Wa-182的NS基因单独转移到野生型A/安阿伯/6/60病毒时,受体表现出完全相同的特征。核苷酸序列分析表明,Wa-182的NS基因相对于野生型NS基因包含三个点突变,导致非结构蛋白NS2中有两个氨基酸替换,这表明NS2蛋白中的突变影响了Wa-182的PA基因的正常复制。结果还表明,NS2蛋白在完整基因组RNA的合成中起重要作用。