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Molecular Evolution of the Human Enteroviruses: Correlation of Serotype with VP1 Sequence and Application to Picornavirus Classification

机译:人类肠道病毒的分子进化:血清型与VP1序列的相关性和在小核糖核酸病毒分类中的应用

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摘要

Sixty-six human enterovirus serotypes have been identified by serum neutralization, but the molecular determinants of the serotypes are unknown. Since the picornavirus VP1 protein contains a number of neutralization domains, we hypothesized that the VP1 sequence should correspond with neutralization (serotype) and, hence, with phylogenetic lineage. To test this hypothesis and to analyze the phylogenetic relationships among the human enteroviruses, we determined the complete VP1 sequences of the prototype strains of 47 human enterovirus serotypes and 10 antigenic variants. Our sequences, together with those available from GenBank, comprise a database of complete VP1 sequences for all 66 human enterovirus serotypes plus additional strains of seven serotypes. Phylogenetic trees constructed from complete VP1 sequences produced the same four major clusters as published trees based on partial VP2 sequences; in contrast to the VP2 trees, however, in the VP1 trees strains of the same serotype were always monophyletic. In pairwise comparisons of complete VP1 sequences, enteroviruses of the same serotype were clearly distinguished from those of heterologous serotypes, and the limits of intraserotypic divergence appeared to be about 25% nucleotide sequence difference or 12% amino acid sequence difference. Pairwise comparisons suggested that coxsackie A11 and A15 viruses should be classified as strains of the same serotype, as should coxsackie A13 and A18 viruses. Pairwise identity scores also distinguished between enteroviruses of different clusters and enteroviruses from picornaviruses of different genera. The data suggest that VP1 sequence comparisons may be valuable in enterovirus typing and in picornavirus taxonomy by assisting in the genus assignment of unclassified picornaviruses.
机译:通过血清中和已经鉴定出66种人肠病毒血清型,但是该血清型的分子决定因素未知。由于小核糖核酸病毒VP1蛋白包含许多中和结构域,因此我们假设VP1序列应与中和(血清型)相对应,因此与系统发生谱系相对应。为了验证这一假设并分析人类肠道病毒之间的系统发育关系,我们确定了47种人类肠道病毒血清型和10种抗原变异体原型菌株的完整VP1序列。我们的序列以及可从GenBank获得的序列组成了一个完整的VP1序列数据库,该数据库包含所有66种人类肠道病毒血清型以及7种血清型的其他菌株。由完整的VP1序列构建的系统发育树与基于部分VP2序列的已发布树产生了相同的四个主要簇。与VP2树相反,在VP1树中,相同血清型的菌株始终是单系的。在完整VP1序列的成对比较中,相同血清型的肠病毒与异源血清型的肠病毒明显区别开来,血清型差异的极限似乎是大约25%核苷酸序列差异或12%氨基酸序列差异。成对比较表明,柯萨奇A11和A15病毒应与柯萨奇A13和A18病毒归为同一血清型。成对的身份评分还可以区分不同簇的肠病毒和不同属的小核糖核酸病毒的肠病毒。数据表明,通过协助未分类的小核糖核酸病毒的属分配,VP1序列比较可能在肠病毒分型和小核糖核酸病毒分类中很有价值。

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