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Molecular evolution of human adenovirus type 16 through multiple recombination events

机译:通过多重重组事件进行人腺病毒16型人腺病毒的分子演变

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Human mastadenoviruses (HAdVs) are non-enveloped, double-stranded DNA viruses that are comprised of more than 85 types classified within seven species (A-G) based on genomics. All HAdV prototypes and many newly defined type genomes have been completely sequenced and are available. Computational analyses of the prototypes and newly emergent HAdV strains provide insights into the evolutionary history and molecular adaptation of HAdV. Most types of HAdV-B are important pathogens causing severe respiratory infections or urinary tract infections and are well characterized. However, HAdV-16 of the B1 subspecies has rarely been reported and its genome is poorly characterized. In this study, bioinformatics analysis, based on genome sequences obtained in GenBank, suggested that HAdV-16, a prototype HAdV-B species, evolved from multiple intertypic recombination events. HAdV-16 genome contains the hexon loop 1 to loop 2 region from HAdV-E4, the partial hexon conserved region 4 (C4) from the subspecies HAdV-B2, genome region 30,897-33,384 containing the fiber gene from SAdV-35, and other genomic parts from the subspecies HAdV-B1. Moreover, analysis of sequence similarity with HAdV-E4 LI, LII, and SAdV-36 strains demonstrated the recombination events happened rather early. Further, amino acid sequence alignment indicated that the amino acid variations occurred in hypervariable regions (HVRs). Especially, the major difference in HVR7, which contains the critical neutralization epitope of HAdV-E4, between HAdV-16 and HAdV-E4 might explain the low level of cross-neutralization between these strains. Our findings promote better understanding on HAdV evolution, predicting newly emergent HAdV strains, and developing novel HAdV vectors.
机译:人乳腺病毒(HADV)是非封闭的双链DNA病毒,其基于基因组学的七种(A-G)内分类为85种以上。所有HADV原型和许多新定义的类型基因组已完全排序并可用。原型的计算分析和新紧急的HADV菌株提供了对哈夫夫的进化史和分子适应的见解。大多数类型的Hadv-B是导致严重呼吸道感染或尿路感染的重要病原体,并且表征得很好。然而,B1亚种的Hadv-16很少报告,其基因组特征很差。在该研究中,基于Genbank中获得的基因组序列的生物信息分析表明,从多个内部重组事件中演化了患有原型Hadv-B物种。 Hadv-16基因组含有来自Hadv-E4的己酮环1到环2区域,含有来自Sadv-35的纤维基因的基因组9,897-33,384,以及来自Sadv-35的纤维基因的部分己克隆保守区4(C4)。来自亚种的基因组零件Hadv-B1。此外,与Hadv-e4锂,刘和Sadv-36菌株的序列相似性分析表明,重组事件发生了相当早。此外,氨基酸序列对准表明氨基酸变化在高变区域(HVR)中发生。特别是HVR7的主要差异,其中含有HADV-16和HADV-E4之间的HADV-E4的临界中和表位可能解释这些菌株之间的次数的较低水平。我们的调查结果促进了对Hadv演变的更好理解,预测新突出的Hadv菌株,以及开发新的Hadv载体。

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