Nerome R, Hiromoto Y, Sugita S, Tanabe N, Ishida M, Matsumoto M, Lindstrom S E, Takahashi T, Nerome K
Department of Virology I, National Institute of Infectious Diseases, Tokyo, Japan.
Arch Virol. 1998;143(8):1569-83. doi: 10.1007/s007050050399.
New antigenic variants of B/Yamagata/16/88-like lineage which appeared in the season of 1997 as a minor strain tended to predominate in the following season. Also, we could observe for the first time, three peaks of activity caused by H3N2 virus and two variants of B influenza virus. Antigenic and phylogenetic analyses revealed that B/Victoria/2/87-like variants appeared again in Japan in 1997 after a nine-year absence. Influenza B viruses evolved into three major lineages, including the earliest strain (I), B/Yamagata/16/88-like variants (II), which comprised of three sublineages (II-(i), II-(ii), II-(iii)), and B/Victoria/2/87-like variants (III). Evolution of influenza B virus hemagglutinin was apparently distinguishable from that of influenza A virus, showing a systematic mechanism of nucleotide deletion and insertion. This phenomenon was observed to be closely related to evolutionary pathways of I, II-(i), II-(ii), II-(iii) and III lineages. It was noteworthy to reveal that the nucleotide deletion and insertion mechanism of influenza B virus completed one cycle over a fifty-year period, and that a three nucleotide deletion was again observed in 1997 strains belonging to lineage II-(iii). It was evident that amino acid substitutions accompanying nucleotide insertions were highly conserved.
1997年作为次要毒株出现的B/山形/16/88样谱系的新抗原变异株在接下来的季节中趋于占主导地位。此外,我们首次观察到由H3N2病毒和两种B型流感病毒变异株引起的三个活动高峰。抗原性和系统发育分析显示,B/维多利亚/2/87样变异株在缺席九年后于1997年再次出现在日本。B型流感病毒进化为三个主要谱系,包括最早的毒株(I)、B/山形/16/88样变异株(II),后者由三个亚谱系(II-(i)、II-(ii)、II-(iii))组成,以及B/维多利亚/2/87样变异株(III)。B型流感病毒血凝素的进化明显不同于A型流感病毒,呈现出核苷酸缺失和插入的系统机制。观察到这种现象与I、II-(i)、II-(ii)、II-(iii)和III谱系的进化途径密切相关。值得注意的是,B型流感病毒的核苷酸缺失和插入机制在五十年的时间里完成了一个循环,并且在1997年属于II-(iii)谱系的毒株中再次观察到三个核苷酸的缺失。显然,伴随核苷酸插入的氨基酸替换具有高度保守性。