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基于全基因组序列的发热、血小板减少和白细胞减少病毒(FTLSV)的分子进化

Molecular evolution of fever, thrombocytopenia and leukocytopenia virus (FTLSV) based on whole-genome sequences.

作者信息

Liu Licheng, Chen Weijun, Yang Yinhui, Jiang Yongqiang

机构信息

State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China.

State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China.

出版信息

Infect Genet Evol. 2016 Apr;39:55-63. doi: 10.1016/j.meegid.2015.12.022. Epub 2015 Dec 31.

Abstract

FTLSV is a novel bunyavirus that was discovered in 2007 in the Henan province of China and has reported case fatality rates of up to 30%. Despite the high case fatality rate, knowledge of the evolution and molecular epidemiology of FTLSV is limited. In this study, detailed phylogenetic analyses were performed on whole-genome sequences to examine the virus's evolutionary rates, estimate dates of common ancestry, and determine the population dynamics and selection pressure for FTLSV. The evolutionary rates of FTLSV were estimated to be 2.28×10(-4), 2.42×10(-4) and 1.19×10(-4) nucleotide substitutions/site/year for the S, M and L segments, respectively. The most recent ancestor of the viruses existed approximately 182-294 years ago. Evidence of RNA segment reassortment was found in FTLSV. A Bayesian skyline plot showed that after a period of genetic stability following high variability, the FTLSV population appeared to have contracted it. Selection pressures were estimated and revealed an abundance of negatively selected sites and sparse positively selected sites. These data will be valuable in understanding the evolution and molecular epidemiology of FTLSV, eventually helping to determine mechanisms of emergence and pathogenicity and the level of the virus's threat to public health.

摘要

阜阳蜱传新型布尼亚病毒(FTLSV)是2007年在中国河南省发现的一种新型布尼亚病毒,报告的病死率高达30%。尽管病死率很高,但对FTLSV的进化和分子流行病学的了解仍然有限。在本研究中,对全基因组序列进行了详细的系统发育分析,以研究该病毒的进化速率、估计共同祖先的日期,并确定FTLSV的种群动态和选择压力。FTLSV的进化速率估计分别为S、M和L片段2.28×10(-4)、2.42×10(-4)和1.19×10(-4)个核苷酸替换/位点/年。这些病毒的最近共同祖先大约存在于182 - 294年前。在FTLSV中发现了RNA片段重配的证据。贝叶斯天际线图显示,在经历高变异性后的一段遗传稳定期后,FTLSV种群似乎出现了收缩。估计了选择压力,结果显示存在大量负选择位点和少量正选择位点。这些数据对于了解FTLSV的进化和分子流行病学具有重要价值,最终有助于确定其出现和致病机制以及该病毒对公众健康的威胁程度。

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