Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 935 Jiaoling Road, Kunming, 650118, Yunnan Province, China.
Kunming Medical University, Kunming, Yunnan, China.
Virus Genes. 2021 Apr;57(2):172-180. doi: 10.1007/s11262-021-01830-3. Epub 2021 Feb 11.
Surveillance of recombinant enterovirus 71 (EV71) and subgenotype replacement is vital for preventing and controlling hand, foot, and mouth disease (HFMD) outbreaks. Despite this, data on recombinant variants and phylogeny of circulating EV71 strains in mainland China are limited. In this study, recombinant variants of EV71 were identified in mainland China from 2009 to 2018. Phylogenetic analysis indicated that except for individual strains (CQ2014-86/CQ/CHN/2014 and EV71/Xiamen/2009 (B5)), almost all of the EV71 strains in mainland China belonged to the subgenotype C4a. Analysing complete genome sequences of 196 EV71 isolates, 3 intertypic recombination strains (VR1432, 30-2/2015/BJ, and Guangdong-2009) and 5 intratypic recombination strains (EV71/P1034/2013, VR1432, Henan-ZMD/CHN/2012, Hubei-WH/CHN/2012, and EV71/P868/2013/China) were identified among naturally circulating EV71. The breakpoints of these recombinant strains were located within the P1, P2, and P3 encoding regions. Notably, a double recombinant (VR1432) resulting from recombination between EV71 subgenotype C4a and C4b strain SHZH98 and a CA8 strain Donovan was identified. This study reports these specific intertypic and intratypic recombination events for the first time highlighting the importance of genetic recombination in the emergence of new enterovirus variants.
对肠道病毒 71 型(EV71)进行重组监测和亚基因型替换对于预防和控制手足口病(HFMD)爆发至关重要。尽管如此,中国大陆流行的 EV71 重组变异株和系统进化数据仍然有限。本研究对 2009 年至 2018 年中国大陆的 EV71 重组变异株进行了鉴定。系统进化分析表明,除个别分离株(CQ2014-86/CQ/CHN/2014 和 EV71/Xiamen/2009(B5))外,中国大陆几乎所有 EV71 分离株均属于 C4a 亚基因型。通过对 196 株 EV71 分离株的全基因组序列进行分析,鉴定出 3 株间重组株(VR1432、30-2/2015/BJ 和广东 2009)和 5 株内重组株(EV71/P1034/2013、VR1432、河南-ZMD/CHN/2012、湖北-WH/CHN/2012 和 EV71/P868/2013/中国)。这些自然循环的 EV71 中存在的重组株的断点位于 P1、P2 和 P3 编码区。值得注意的是,鉴定出一种由 EV71 亚基因型 C4a 和 C4b 株 SHZH98 与 CA8 株 Donovan 之间重组产生的双重重组(VR1432)。本研究首次报道了这些特定的间型和内型重组事件,强调了遗传重组在新肠道病毒变异株出现中的重要性。