Cheung Peter Pak-Hang, Rogozin Igor B, Choy Ka-Tim, Ng Hoi Yee, Peiris Joseph Sriyal Malik, Yen Hui-Ling
School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong.
National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20894-6075, USA.
RNA. 2015 Jan;21(1):36-47. doi: 10.1261/rna.045369.114. Epub 2014 Nov 17.
The error-prone RNA-dependent RNA polymerase (RdRP) and external selective pressures are the driving forces for RNA viral diversity. When confounded by selective pressures, it is difficult to assess if influenza A viruses (IAV) that have a wide host range possess comparable or distinct spontaneous mutational frequency in their RdRPs. We used in-depth bioinformatics analyses to assess the spontaneous mutational frequencies of two RdRPs derived from human seasonal (A/Wuhan/359/95; Wuhan) and H5N1 (A/Vietnam/1203/04; VN1203) viruses using the mini-genome system with a common firefly luciferase reporter serving as the template. High-fidelity reverse transcriptase was applied to generate high-quality mutational spectra which allowed us to assess and compare the mutational frequencies and mutable motifs along a target sequence of the two RdRPs of two different subtypes. We observed correlated mutational spectra (τ correlation P < 0.0001), comparable mutational frequencies (H3N2:5.8 ± 0.9; H5N1:6.0 ± 0.5), and discovered a highly mutable motif "(A)AAG" for both Wuhan and VN1203 RdRPs. Results were then confirmed with two recombinant A/Puerto Rico/8/34 (PR8) viruses that possess RdRP derived from Wuhan or VN1203 (RG-PR8×Wuhan(PB2, PB1, PA, NP) and RG-PR8×VN1203(PB2, PB1, PA, NP)). Applying novel bioinformatics analysis on influenza mutational spectra, we provide a platform for a comprehensive analysis of the spontaneous mutation spectra for an RNA virus.
易出错的RNA依赖性RNA聚合酶(RdRP)和外部选择压力是RNA病毒多样性的驱动力。当受到选择压力的干扰时,很难评估具有广泛宿主范围的甲型流感病毒(IAV)在其RdRP中是否具有可比或不同的自发突变频率。我们使用深入的生物信息学分析,以常见的萤火虫荧光素酶报告基因作为模板,通过微型基因组系统评估源自人类季节性(A/武汉/359/95;武汉)和H5N1(A/越南/1203/04;VN1203)病毒的两种RdRP的自发突变频率。应用高保真逆转录酶生成高质量的突变谱,这使我们能够评估和比较两种不同亚型的两种RdRP的目标序列上的突变频率和可变基序。我们观察到相关的突变谱(τ相关性P<0.0001)、可比突变频率(H3N2:5.8±0.9;H5N1:6.0±0.5),并发现武汉和VN1203 RdRP均有一个高度可变基序“(A)AAG”。然后用两种重组A/波多黎各/8/34(PR8)病毒进行了验证,这两种病毒分别含有源自武汉或VN1203的RdRP(RG-PR8×武汉(PB2、PB1、PA、NP)和RG-PR8×VN1203(PB2、PB1、PA、NP))。通过对流感突变谱进行新颖的生物信息学分析,我们为全面分析RNA病毒的自发突变谱提供了一个平台。