Shu L L, Bean W J, Webster R G
Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38101.
J Virol. 1993 May;67(5):2723-9. doi: 10.1128/JVI.67.5.2723-2729.1993.
This study examined the evolution and variation of the human influenza virus nucleoprotein gene from the earliest isolates to the present. Phylogenetic reconstruction of the most parsimonious evolutionary path connecting 49 nucleoprotein sequences yielded a single lineage. The average calculated rate of mutation was 3.6 nucleotide substitutions per year (2.3 x 10(-3) substitutions per site per year). Thirty-two percent of these mutations resulted in amino acid substitutions, and the remainder were silent mutations. Analysis of virus isolates from China and elsewhere showed no significant differences in their rate of evolution, genetic diversity, or mean survival time. The nearly constant rate of change was maintained through the two antigenic shifts, and there were no obvious changes in the number or types of mutations associated with the changes in the surface proteins. A detailed comparison of the changes that have occurred on the main evolutionary path with those that have occurred on the side branches of the phylogenetic tree was made. This showed that while 35% of the mutations on the side branches resulted in amino acid changes, only 21% of those on the main path affected the protein sequence. These results suggest that although the rate of change of the human influenza virus nucleoprotein is much higher than that previously described for avian influenza viruses, there are measurable constraints on the evolution of the surviving virus lineage. Comparison of the nucleoproteins of virus isolates adapted to chicken embryos with the nucleoproteins of those grown only in MDCK cells revealed no consistent differences between the virus pairs. Thus, although the nucleoprotein is known to be critical for host specificity, its adaptation to growth in eggs apparently involves no immediate selective pressures, such as are found with hemagglutinin.
本研究考察了人类流感病毒核蛋白基因从最早分离株到目前的进化与变异情况。对连接49个核蛋白序列的最简约进化路径进行系统发育重建,得到了一个单一谱系。计算得出的平均突变率为每年3.6个核苷酸替换(每个位点每年2.3×10⁻³个替换)。这些突变中32%导致氨基酸替换,其余为沉默突变。对来自中国和其他地区的病毒分离株的分析表明,它们在进化速率、遗传多样性或平均存活时间上没有显著差异。在两次抗原转变过程中,变化速率几乎保持恒定,并且与表面蛋白变化相关的突变数量或类型没有明显变化。对主要进化路径上发生的变化与系统发育树侧枝上发生的变化进行了详细比较。结果表明,虽然侧枝上35%的突变导致氨基酸变化,但主要路径上只有21%的突变影响蛋白质序列。这些结果表明,尽管人类流感病毒核蛋白的变化速率远高于先前描述的禽流感病毒,但存活病毒谱系的进化存在可测量的限制。将适应鸡胚的病毒分离株的核蛋白与仅在MDCK细胞中生长的病毒分离株的核蛋白进行比较,发现病毒对之间没有一致的差异。因此,尽管已知核蛋白对宿主特异性至关重要,但其适应在鸡蛋中生长显然不涉及诸如血凝素所具有的直接选择压力。