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人类16型腺病毒通过多次重组事件的分子进化

Molecular evolution of human adenovirus type 16 through multiple recombination events.

作者信息

Tian Xingui, Wu Hongkai, Zhou Rong

机构信息

State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, China.

出版信息

Virus Genes. 2019 Dec;55(6):769-778. doi: 10.1007/s11262-019-01698-4. Epub 2019 Aug 5.

DOI:10.1007/s11262-019-01698-4
PMID:31385187
Abstract

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.

摘要

人腺病毒(HAdVs)是无包膜的双链DNA病毒,根据基因组学可分为7个种(A - G),包含85种以上的类型。所有HAdV原型和许多新定义的类型基因组都已完成全序列测定并可供使用。对原型和新出现的HAdV毒株的计算分析为HAdV的进化历史和分子适应性提供了见解。大多数HAdV - B型是引起严重呼吸道感染或尿路感染的重要病原体,且特征明确。然而,B1亚种的HAdV - 16很少被报道,其基因组特征也很差。在本研究中,基于从GenBank获得的基因组序列进行的生物信息学分析表明,HAdV - 16作为HAdV - B种的原型,是由多个型间重组事件进化而来的。HAdV - 16基因组包含来自HAdV - E4的六邻体环1至环2区域、来自HAdV - B2亚种的部分六邻体保守区域4(C4)、包含来自SAdV - 35的纤维基因的基因组区域30,897 - 33,384,以及来自HAdV - B1亚种的其他基因组部分。此外,与HAdV - E4 LI、LII和SAdV - 36毒株的序列相似性分析表明重组事件发生得相当早。进一步的氨基酸序列比对表明氨基酸变异发生在高变区(HVRs)。特别是,HAdV - 16和HAdV - E4之间HVR7的主要差异,其中包含HAdV - E4的关键中和表位,可能解释了这些毒株之间交叉中和水平较低的原因。我们的发现有助于更好地理解HAdV的进化、预测新出现的HAdV毒株以及开发新型HAdV载体。

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