Neurovirology Project, Tokyo Metropolitan Institute of Medical Sciencegrid.272456.0, Tokyo, Japan.
Virus Research Center, Clinical Research Division, Sendai Medical Centergrid.415495.8, Sendai, Japan.
J Virol. 2021 Nov 9;95(23):e0151521. doi: 10.1128/JVI.01515-21. Epub 2021 Sep 15.
Although epidemics of hand, foot, and mouth disease (HFMD) caused by enterovirus A71 (EV-A71) have occurred worldwide, the Asia-Pacific region has seen large sporadic outbreaks with many severe neurological cases. This suggests that the virulence of the circulating viruses fluctuates in each epidemic and that HFMD outbreaks with many severe cases occur when highly virulent viruses are circulating predominantly, which has not been experimentally verified. Here, we analyzed 32 clinically isolated strains obtained in Japan from 2002 to 2013, along with 27 Vietnamese strains obtained from 2015 to 2016 that we characterized previously using human SCARB2 transgenic mice. Phylogenetic analysis of the P1 region classified them into five clades belonging to subgenogroup B5 (B5-I to B5-V) and five clades belonging to subgenogroup C4 (C4-I to C4-V) according to the epidemic year and region. Interestingly, clades B5-I and B5-II were very virulent, while clades B5-III, B5-IV, and B5-V were less virulent. Clades C4-II, C4-III, C4-IV, and C4-V were virulent, while clade C4-I was not. The result experimentally showed for the first time that several clades with different virulence levels emerged one after another. The experimental virulence evaluation of circulating viruses using SCARB2 transgenic mice is helpful to assess potential risks of circulating viruses. These results also suggest that a minor nucleotide or amino acid substitution in the EV-A71 genome during circulation causes fluctuations in virulence. The data presented here may increase our understanding of the dynamics of viral virulence during epidemics. Outbreaks of hand, foot, and mouth disease (HFMD) with severe enterovirus A71 (EV-A71) cases have occurred repeatedly, mainly in Asia. In severe cases, central nervous system complications can lead to death, making it an infectious disease of importance to public health. An unanswered question about this disease is why outbreaks of HFMD with many severe cases sometimes occur. Here, we collected EV-A71 strains that were prevalent in Japan and Vietnam over the past 20 years and evaluated their virulence in a mouse model of EV-A71 infection. This method clearly revealed that viruses belonging to different clades have different virulence, indicating that the method is powerful to assess the potential risks of the circulating viruses. The results also suggested that factors in the virus genome cause an outbreak with many severe cases and that further studies facilitate the prediction of large epidemics of EV-A71 in the future.
虽然肠道病毒 A71(EV-A71)引起的手足口病(HFMD)在全球范围内时有发生,但在亚太地区,曾出现过多次大规模散发疫情,并有许多严重的神经科病例。这表明循环病毒的毒力在每次流行中都有波动,并且当主要流行高毒力病毒时,会出现HFMD 爆发和许多严重病例,这尚未通过实验验证。在这里,我们分析了 2002 年至 2013 年期间在日本从临床分离得到的 32 株病毒,以及 2015 年至 2016 年期间我们以前使用人 SCARB2 转基因小鼠鉴定的 27 株越南病毒株。对 P1 区的系统进化分析将它们根据流行年份和地区分为五个亚组 B5(B5-I 至 B5-V)和五个亚组 C4(C4-I 至 C4-V)的分支。有趣的是,B5-I 和 B5-II 分支非常毒力,而 B5-III、B5-IV 和 B5-V 分支毒力较弱。C4-II、C4-III、C4-IV 和 C4-V 分支毒力较强,而 C4-I 分支则没有。该实验结果首次表明,不同毒力水平的几个分支相继出现。使用 SCARB2 转基因小鼠对循环病毒的实验性毒力评估有助于评估循环病毒的潜在风险。这些结果还表明,EV-A71 基因组在循环过程中发生的微小核苷酸或氨基酸替换会导致毒力波动。本文提供的数据可能会增加我们对手足口病病毒毒力在流行过程中动态变化的认识。 手足口病(HFMD)的爆发和严重肠道病毒 A71(EV-A71)病例反复发生,主要在亚洲。在严重的情况下,中枢神经系统并发症可导致死亡,使其成为一种对公共卫生具有重要意义的传染病。关于这种疾病的一个悬而未决的问题是,为什么有时会爆发 HFMD 并有许多严重病例。在这里,我们收集了过去 20 年来在日本和越南流行的 EV-A71 菌株,并在 EV-A71 感染的小鼠模型中评估了它们的毒力。这种方法清楚地表明,属于不同分支的病毒具有不同的毒力,表明该方法能够有力地评估循环病毒的潜在风险。结果还表明,病毒基因组中的因素导致了严重病例的爆发,进一步的研究有助于未来预测 EV-A71 的大规模流行。