Mizukoshi Fuminori, Nagasawa Koo, Doan Yen H, Haga Kei, Yoshizumi Shima, Ueki Yo, Shinohara Michiyo, Ishikawa Mariko, Sakon Naomi, Shigemoto Naoki, Okamoto-Nakagawa Reiko, Ochi Akie, Murakami Koichi, Ryo Akihide, Suzuki Yoshiyuki, Katayama Kazuhiko, Kimura Hirokazu
Department of Microbiology, Tochigi Prefectural Institute of Public Health and Environmental ScienceUtsunomiya-shi, Japan.
Infectious Disease Surveillance Center, National Institute of Infectious DiseasesMusashimurayama-shi, Japan.
Front Microbiol. 2017 Apr 25;8:705. doi: 10.3389/fmicb.2017.00705. eCollection 2017.
The RNA-dependent RNA polymerase () and capsid () genes of 51 GII.2 human norovirus (HuNoV) strains collected during the period of 2004-2015 in Japan were analyzed. Full-length analyses of the genes were performed using next-generation sequencing. Based on the gene sequences, we constructed the time-scale evolutionary trees by Bayesian Markov chain Monte Carlo methods. Time-scale phylogenies showed that the and genes evolved uniquely and independently. Four genotypes of GII.2 (major types: GII.P2-GII.2 and GII.P16-GII.2) were detected. A common ancestor of the GII.2 gene existed until about 1956. The evolutionary rates of the genes were high (over 10 substitutions/site/year). Moreover, the gene evolution may depend on the gene. Based on these results, we hypothesized that transfer of the gene accelerated the gene evolution of HuNoV genotype GII.2. Consequently, recombination between ORF1 (polymerase) and ORF2 (capsid) might promote changes of GII.2 antigenicity.
对2004年至2015年期间在日本收集的51株GII.2型人诺如病毒(HuNoV)的RNA依赖性RNA聚合酶()和衣壳()基因进行了分析。使用下一代测序技术对这些基因进行了全长分析。基于基因序列,我们通过贝叶斯马尔可夫链蒙特卡罗方法构建了时间尺度进化树。时间尺度系统发育分析表明,和基因独特且独立地进化。检测到四种GII.2基因型(主要类型:GII.P2-GII.2和GII.P16-GII.2)。GII.2基因的一个共同祖先一直存在到大约1956年。这些基因的进化速率很高(超过10个替换/位点/年)。此外,基因进化可能依赖于基因。基于这些结果,我们推测基因的转移加速了HuNoV基因型GII.2的基因进化。因此,ORF1(聚合酶)和ORF2(衣壳)之间的重组可能促进GII.2抗原性的变化。