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人呼吸道病毒3融合蛋白()基因的分子进化

Molecular Evolution of the Fusion Protein () Gene in Human Respirovirus 3.

作者信息

Aso Jumpei, Kimura Hirokazu, Ishii Haruyuki, Saraya Takeshi, Kurai Daisuke, Matsushima Yuki, Nagasawa Koo, Ryo Akihide, Takizawa Hajime

机构信息

Department of Respiratory Medicine, School of Medicine, Kyorin University, Tokyo, Japan.

Department of Health Science, Graduate School of Health Science, Gunma Paz University, Gunma, Japan.

出版信息

Front Microbiol. 2020 Jan 15;10:3054. doi: 10.3389/fmicb.2019.03054. eCollection 2019.

Abstract

To elucidate the evolution of human respirovirus 3 (HRV3), we performed detailed genetic analyses of the gene (full-length) detected from hundreds of HRV3 strains obtained from various geographic regions. First, we performed time-scaled evolutionary analyses using the Bayesian Markov chain Monte Carlo method. Then, we performed analyses of phylodynamics, similarity, phylogenetic distance, selective pressure, and conformational B-cell epitope with the F-protein structural analyses. Time-scaled phylogenetic tree showed that the common ancestor of HRV3 and bovine respirovirus 3 diverged over 300 years ago and subdivided it into three major clusters and four subclusters during the most recent 100 years. The overall evolutionary rate was approximately 10 substitutions/site/year. Indigenous similarity was seen in the present strains, and the mean phylogenetic distance were 0.033. Many negative selection sites were seen in the ectodomain. The conformational epitopes did not correspond to the neutralizing antibody binding sites. These results suggest that the HRV3 gene is relatively conserved and restricted in this diversity to preserve the protein function, although these strains form many branches on the phylogenetic tree. Furthermore, HRV3 reinfection may be responsible for discordances between the conformational epitopes and the neutralizing antibody binding sites of the F protein. These findings contribute to a better understanding of HRV3 virology.

摘要

为阐明人呼吸道病毒3型(HRV3)的进化情况,我们对从不同地理区域获得的数百株HRV3毒株中检测到的基因(全长)进行了详细的遗传分析。首先,我们使用贝叶斯马尔可夫链蒙特卡罗方法进行了时间尺度的进化分析。然后,我们结合F蛋白结构分析对系统动力学、相似性、系统发育距离、选择压力和构象B细胞表位进行了分析。时间尺度系统发育树显示,HRV3和牛呼吸道病毒3型的共同祖先在300多年前分化,并在最近100年内细分为三个主要簇和四个亚簇。总体进化速率约为每年每位点10个替换。在当前毒株中观察到本土相似性,平均系统发育距离为0.033。在外结构域中发现了许多负选择位点。构象表位与中和抗体结合位点不对应。这些结果表明,尽管这些毒株在系统发育树上形成了许多分支,但HRV3基因相对保守,且在这种多样性中受到限制以保持蛋白质功能。此外,HRV3再次感染可能是F蛋白的构象表位与中和抗体结合位点之间不一致的原因。这些发现有助于更好地理解HRV3病毒学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/352e/6974460/d9080f8c51fa/fmicb-10-03054-g001.jpg

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