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基于马尔可夫链蒙特卡罗的贝叶斯模型在寨卡病毒基因进化与动态变化分析中的应用

Application of MCMC-Based Bayesian Modeling for Genetic Evolutionary and Dynamic Change Analysis of Zika Virus.

作者信息

Shao Tong, Pan Jiahui, Zhang Shiwei, Xin Zhuoyuan, Wang Guoqing

机构信息

Department of Pathogenobiology, The Key Laboratory of Zoonosis, Chinese Ministry of Education, College of Basic Medical Science, Jilin University, Changchun, China.

The Key Laboratory for Bionics Engineering, Ministry of Education, China, Jilin University, Changchun, China.

出版信息

Front Genet. 2020 Jan 10;10:1319. doi: 10.3389/fgene.2019.01319. eCollection 2019.

Abstract

Zika virus was first discovered in 1947. For a long time afterward, no large-scale outbreaks occurred. However, more recently, in 2007 and 2016, there were two episodes of ZIKV outbreak that have produced serious public health problems. By analyzing the evolution of the viral genome, we can understand the potential for its outbreak. In this study, we constructed a maximum clade credibility (MCC) tree for the ZIKV non-structural protein 5 (NS5) gene using the Bayesian method. A total of 108 whole-NS5 sequences were retrieved from the GeneBank. We carried out an analysis of potential glycosylation and phosphorylation sites of the ZIKV virus NS5 gene and dynamic analysis of the evolutionary characteristics of the gene. Phylogenetic analysis revealed the presence of two sequence lineages: African and Asian. The sequence of the strains obtained from GeneBank has high homology of 85% to 100%. There are 35 potential phosphorylation sites and glycosylation sites in the ZIKV-NS5 sequences. This article analyzes the possible causes of ZIKV virus outbreaks from the perspective of genetic evolution and analyzes the dynamic trends of virus outbreaks to provide a theoretical basis for predicting the outbreak of the virus.

摘要

寨卡病毒于1947年首次被发现。在那之后的很长一段时间里,没有发生大规模疫情。然而,最近在2007年和2016年,发生了两起寨卡病毒疫情,产生了严重的公共卫生问题。通过分析病毒基因组的进化,我们可以了解其爆发的可能性。在本研究中,我们使用贝叶斯方法构建了寨卡病毒非结构蛋白5(NS5)基因的最大分支可信度(MCC)树。从基因库中检索到总共108条完整的NS5序列。我们对寨卡病毒NS5基因的潜在糖基化和磷酸化位点进行了分析,并对该基因的进化特征进行了动态分析。系统发育分析揭示了两个序列谱系的存在:非洲谱系和亚洲谱系。从基因库获得的毒株序列具有85%至100%的高同源性。寨卡病毒NS5序列中有35个潜在的磷酸化位点和糖基化位点。本文从基因进化的角度分析了寨卡病毒爆发的可能原因,并分析了病毒爆发的动态趋势,为预测该病毒的爆发提供理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fd/6967594/79137ccfa97d/fgene-10-01319-g001.jpg

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