Oberste M Steven, Peñaranda Silvia, Maher Kaija, Pallansch Mark A
Respiratory and Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop G-17, Atlanta, GA 30333, USA.
J Gen Virol. 2004 Jun;85(Pt 6):1597-1607. doi: 10.1099/vir.0.79789-0.
The species Human enterovirus A (HEV-A) in the family Picornaviridae consists of coxsackieviruses (CV) A2-A8, A10, A12, A14 and A16 and enterovirus 71. Complete genome sequences for the prototype strains of the 10 serotypes whose sequences were not represented in public databases have been determined and analysed in conjunction with previously available complete sequences in GenBank. Members of HEV-A are monophyletic relative to all other human enterovirus species in all regions of the genome except in the 5' non-translated region (NTR), where they are known to cluster with members of HEV-B. The HEV-A prototype strains were about 66 to 86 % identical to one another in deduced capsid amino acid sequence. Antigenic cross-reactivity has been reported between CVA3-Olson and CVA8-Donovan, between CVA5-Swartz and CVA12-Texas-12 and between CVA16-G-10 and EV71-BrCr. Similarity plots, individual sequence comparisons and phylogenetic analyses demonstrate a high degree of capsid sequence similarity within each of these three pairs of prototype strains, providing a molecular basis for the observed antigenic relationships. In several cases, phylogenies constructed from the structural (P1) and non-structural regions of the genome (P2 and P3) are incongruent. The incongruent phylogenies and the similarity plot analyses imply that recombination has played a role in the evolution of the HEV-A prototype strains. CVA6-Gdula clearly contains sequences that are also present in CVA10-Kowalik and CVA12-Texas-12, suggesting that these three strains have a shared evolutionary history despite their lack of similarity in the capsid region.
微小核糖核酸病毒科中的人类肠道病毒A(HEV-A)包括柯萨奇病毒(CV)A2 - A8、A10、A12、A14和A16以及肠道病毒71型。已确定并分析了10种血清型原型毒株的完整基因组序列,这些序列在公共数据库中未被收录,并结合了GenBank中先前可用的完整序列进行分析。除了5'非翻译区(NTR)外,HEV-A的成员在基因组的所有区域相对于所有其他人类肠道病毒种类都是单系的,已知它们在5'非翻译区与HEV-B的成员聚类。HEV-A原型毒株在推导的衣壳氨基酸序列上彼此之间约有66%至86%的同一性。据报道,CVA3 - Olson与CVA8 - Donovan、CVA5 - Swartz与CVA12 - Texas - 12以及CVA16 - G - 10与EV71 - BrCr之间存在抗原交叉反应。相似性图谱、个体序列比较和系统发育分析表明,这三对原型毒株中的每一对在衣壳序列上都有高度相似性,为观察到的抗原关系提供了分子基础。在几种情况下,由基因组的结构(P1)和非结构区域(P2和P3)构建的系统发育树是不一致的。不一致的系统发育树和相似性图谱分析表明,重组在HEV-A原型毒株的进化中发挥了作用。CVA6 - Gdula明显包含也存在于CVA10 - Kowalik和CVA12 - Texas - 12中的序列,这表明这三种毒株尽管在衣壳区域缺乏相似性,但具有共同的进化历史。