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Molecular evolution of the VP1 VP2 and VP3 genes in human rhinovirus species C

机译:人类鼻病毒种C中VP1VP2和VP3基因的分子进化

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摘要

Human rhinovirus species C (HRV-C) was recently discovered, and this virus has been associated with various acute respiratory illnesses (ARI). However, the molecular evolution of the major antigens of this virus, including VP1, VP2, and VP3, is unknown. Thus, we performed complete VP1, VP2, and VP3 gene analyses of 139 clinical HRV-C strains using RT-PCR with newly designed primer sets and next-generation sequencing. We assessed the time-scale evolution and evolutionary rate of these genes using the Bayesian Markov chain Monte Carlo method. In addition, we calculated the pairwise distance and confirmed the positiveegative selection sites in these genes. The phylogenetic trees showed that the HRV-C strains analyzed using these genes could be dated back approximately 400 to 900 years, and these strains exhibited high evolutionary rates (1.35 to 3.74 × 10−3 substitutions/site/year). Many genotypes (>40) were confirmed in the phylogenetic trees. Furthermore, no positively selected site was found in the VP1, VP2, and VP3 protein. Molecular modeling analysis combined with variation analysis suggested that the exterior surfaces of the VP1, VP2 and VP3 proteins are rich in loops and are highly variable. These results suggested that HRV-C may have an old history and unique antigenicity as an agent of various ARI.
机译:最近发现了人类鼻病毒C(HRV-C),这种病毒与各种急性呼吸道疾病(ARI)有关。但是,该病毒的主要抗原,包括VP1,VP2和VP3的分子进化是未知的。因此,我们使用具有新设计的引物组和下一代测序的RT-PCR对139例临床HRV-C菌株进行了完整的VP1,VP2和VP3基因分析。我们使用贝叶斯马尔可夫链蒙特卡洛方法评估了这些基因的时标进化和进化速率。此外,我们计算了成对距离并确认了这些基因中的正/负选择位点。系统进化树表明,使用这些基因分析的HRV-C菌株可以追溯到大约400至900年,并且这些菌株表现出高进化速率(1.35至3.74×10 −3 取代/位点/年)。在系统发育树中证实了许多基因型(> 40)。此外,在VP1,VP2和VP3蛋白中未发现阳性选择位点。分子建模分析与变异分析相结合,表明VP1,VP2和VP3蛋白的外表面富含环且高度可变。这些结果表明,HRV-C作为各种ARI的病因可能具有悠久的历史和独特的抗原性。

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