Department of Microbiology, College of Medicine and Medical Research Institute, Chungbuk National University, 12 Gaeshin-Dong Heungduk-Ku, Cheongju City, 361-763, Republic of Korea.
J Virol. 2011 Jul;85(13):6275-86. doi: 10.1128/JVI.02125-10. Epub 2011 Apr 20.
Gene mutations and reassortment are key mechanisms by which influenza A virus acquires virulence factors. To evaluate the role of the viral polymerase replication machinery in producing virulent pandemic (H1N1) 2009 influenza viruses, we generated various polymerase point mutants (PB2, 627K/701N; PB1, expression of PB1-F2 protein; and PA, 97I) and reassortant viruses with various sources of influenza viruses by reverse genetics. Although the point mutations produced no significant change in pathogenicity, reassortment between the pandemic A/California/04/09 (CA04, H1N1) and current human and animal influenza viruses produced variants possessing a broad spectrum of pathogenicity in the mouse model. Although most polymerase reassortants had attenuated pathogenicity (including those containing seasonal human H3N2 and high-pathogenicity H5N1 virus segments) compared to that of the parental CA04 (H1N1) virus, some recombinants had significantly enhanced virulence. Unexpectedly, one of the five highly virulent reassortants contained a A/Swine/Korea/JNS06/04(H3N2)-like PB2 gene with no known virulence factors; the other four had mammalian-passaged avian-like genes encoding PB2 featuring 627K, PA featuring 97I, or both. Overall, the reassorted polymerase complexes were only moderately compatible for virus rescue, probably because of disrupted molecular interactions involving viral or host proteins. Although we observed close cooperation between PB2 and PB1 from similar virus origins, we found that PA appears to be crucial in maintaining viral gene functions in the context of the CA04 (H1N1) virus. These observations provide helpful insights into the pathogenic potential of reassortant influenza viruses composed of the pandemic (H1N1) 2009 influenza virus and prevailing human or animal influenza viruses that could emerge in the future.
基因突变和重配是甲型流感病毒获得毒力因子的关键机制。为了评估病毒聚合酶复制机制在产生高致病性大流行(H1N1)2009 流感病毒中的作用,我们通过反向遗传学生成了各种聚合酶点突变(PB2,627K/701N;PB1,表达 PB1-F2 蛋白;和 PA,97I)和具有不同来源流感病毒的重组病毒。尽管点突变对致病性没有显著影响,但大流行 A/加利福尼亚/04/09(CA04,H1N1)与当前人和动物流感病毒之间的重配产生了在小鼠模型中具有广泛致病性的变体。虽然大多数聚合酶重组体的致病性减弱(包括含有季节性人 H3N2 和高致病性 H5N1 病毒片段的重组体)与亲本 CA04(H1N1)病毒相比,但有些重组体的毒力显著增强。出乎意料的是,五种高致病性重组体中有一个含有 A/猪/韩国/JNS06/04(H3N2)样 PB2 基因,没有已知的毒力因子;其他四个具有哺乳动物传代的禽样基因,编码 PB2 具有 627K、PA 具有 97I 或两者兼有。总的来说,重组聚合酶复合物仅具有中等程度的病毒拯救相容性,可能是由于涉及病毒或宿主蛋白的分子相互作用被破坏。尽管我们观察到来自类似病毒起源的 PB2 和 PB1 之间的密切合作,但我们发现 PA 似乎在维持 CA04(H1N1)病毒背景下的病毒基因功能方面至关重要。这些观察结果为构成大流行(H1N1)2009 流感病毒和未来可能出现的流行人和动物流感病毒的重组流感病毒的致病潜力提供了有价值的见解。