Department of Biology, University of Nebraska at Omaha, Omaha, NE 68182-0040, United States.
Infect Genet Evol. 2011 Dec;11(8):2125-32. doi: 10.1016/j.meegid.2011.07.002. Epub 2011 Jul 7.
Influenza A viral nucleoprotein (NP) plays a critical role in virus replication and host adaptation, however, the underlying molecular evolutionary dynamics of NP lineages are less well-understood. In this study, large-scale analyses of 5094 NP nucleotide sequences revealed eight distinct evolutionary lineages, including three host-specific lineages (human, classical swine and equine), two cross-host lineages (Eurasian avian-like swine and swine-origin human pandemic H1N1 2009) and three geographically isolated avian lineages (Eurasian, North American and Oceanian). The average nucleotide substitution rate of the NP lineages was estimated to be 2.4 × 10(-3) substitutions per site per year, with the highest value observed in pandemic H1N1 2009 (3.4 × 10(-3)) and the lowest in equine (0.9 × 10(-3)). The estimated time of most recent common ancestor (TMRCA) for each lineage demonstrated that the earliest human lineage was derived around 1906, and the latest pandemic H1N1 2009 lineage dated back to December 17, 2008. A marked time gap was found between the times when the viruses emerged and were first sampled, suggesting the crucial role for long-term surveillance of newly emerging viruses. The selection analyses showed that human lineage had six positive selection sites, whereas pandemic H1N1 2009, classical swine, Eurasian avian and Eurasian swine had only one or two sites. Protein structure analyses revealed several positive selection sites located in epitope regions or host adaptation regions, indicating strong adaptation to host immune system pressures in influenza viruses. Along with previous studies, this study provides new insights into the evolutionary dynamics of influenza A NP lineages. Further lineage analyses of other gene segments will allow better understanding of influenza A virus evolution and assist in the improvement of global influenza surveillance.
甲型流感病毒核蛋白(NP)在病毒复制和宿主适应中发挥着关键作用,但 NP 谱系的潜在分子进化动态还不太清楚。在这项研究中,对 5094 个 NP 核苷酸序列进行了大规模分析,揭示了 8 个不同的进化谱系,包括 3 个宿主特异性谱系(人、经典猪和马)、2 个跨宿主谱系(欧亚类禽猪和猪源人甲型 H1N1 2009 大流行)和 3 个地理隔离的禽谱系(欧亚、北美和大洋洲)。NP 谱系的平均核苷酸替换率估计为每年每个位点 2.4×10(-3)个替换,其中大流行 H1N1 2009 观察到的最高值(3.4×10(-3)),马的最低值(0.9×10(-3))。每个谱系最近共同祖先(TMRCA)的估计时间表明,最早的人谱系可追溯到 1906 年左右,而最新的大流行 H1N1 2009 谱系可追溯到 2008 年 12 月 17 日。发现病毒出现和首次采样之间存在明显的时间差距,这表明对新出现病毒进行长期监测至关重要。选择分析表明,人谱系有 6 个正选择位点,而大流行 H1N1 2009、经典猪、欧亚禽和欧亚猪只有 1 或 2 个位点。蛋白质结构分析显示,几个正选择位点位于表位或宿主适应区,表明流感病毒对宿主免疫系统压力有很强的适应能力。与之前的研究一起,这项研究为甲型流感 NP 谱系的进化动态提供了新的见解。对其他基因片段的进一步谱系分析将有助于更好地理解甲型流感病毒的进化,并有助于改善全球流感监测。