Solorzano A, Zheng H, Fodor E, Brownlee G G, Palese P, García-Sastre A
Department of Microbiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029-6574, USA.
J Gen Virol. 2000 Mar;81(Pt 3):737-42. doi: 10.1099/0022-1317-81-3-737.
We have previously obtained four transfectant influenza A viruses containing neuraminidase (NA) genes with mutated base pairs in the conserved double-stranded RNA region of the viral promoter by using a ribonucleoprotein transfection system. Two mutant viruses (D2 and D1/2) which share a C-G-->A-U mutation at positions 11 and 12 of the 3' and 5' ends, respectively, of the NA gene, showed an approximate 10-fold reduction of NA-specific mRNA and protein levels (Fodor et al., Journal of Virology 72, 6283-6290, 1998). These viruses have now allowed us to determine the effects of decreased NA levels on virus pathogenicity. Both D2 and D1/2 viruses were highly attenuated in mice, and their replication in mouse lungs was highly compromised as compared with wild-type influenza A/WSN/33 virus. The results highlight the importance of the level of NA activity in the biological cycle and virulence of influenza viruses. Importantly, mice immunized by a single intranasal administration of 10(3) infectious units of D2 or D1/2 viruses were protected against challenge with a lethal dose of wild-type influenza virus. Attenuation of influenza viruses by mutations resulting in the decreased expression of a viral protein represents a novel strategy which could be considered for the generation of live attenuated influenza virus vaccines.
我们之前通过使用核糖核蛋白转染系统,获得了四种转染型甲型流感病毒,这些病毒的神经氨酸酶(NA)基因在病毒启动子保守的双链RNA区域存在碱基对突变。两种突变病毒(D2和D1/2),分别在NA基因3'端和5'端的第11和12位共享一个C-G→A-U突变,其NA特异性mRNA和蛋白水平降低了约10倍(福多尔等人,《病毒学杂志》72,6283 - 6290,1998)。现在,这些病毒使我们能够确定NA水平降低对病毒致病性的影响。D2和D1/2病毒在小鼠中均高度减毒,与野生型甲型流感病毒A/WSN/33相比,它们在小鼠肺中的复制受到严重损害。这些结果突出了NA活性水平在流感病毒生物周期和毒力中的重要性。重要的是,通过单次鼻内接种10³个感染单位的D2或D1/2病毒免疫的小鼠,可免受致死剂量野生型流感病毒的攻击。通过导致病毒蛋白表达降低的突变来减毒流感病毒,代表了一种可用于生产减毒活流感病毒疫苗的新策略。