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Short communication: Molecular epidemiology, phylogeny, and phylodynamics of CRF63-02A1, a recently originated HIV-1 circulating recombinant form spreading in Siberia

机译:简短交流:CRF63-02A1的分子流行病学,系统发育和系统动力学,这是一种最近在西伯利亚传播的HIV-1循环重组形式

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摘要

The HIV-1 epidemic in Russia is dominated by the former Soviet Union subtype A (AFSU) variant, but other genetic forms are circulating in the country. One is the recently described CRF63-02A1, derived from recombination between a CRF02-AG variant circulating in Central Asia and A FSU, which has spread in the Novosibirsk region, Siberia. Here we phylogenetically analyze pol and env segments from 24 HIV-1 samples from the Novosibirsk region collected in 2013, with characterization of three new near full-length genome CRF63-02A1 sequences, and estimate the time of the most recent common ancestor (tMRCA) and the demographic growth of CRF63-02A1 using a Bayesian method. The analyses revealed that CRF63-02A1 is highly predominant in the Novosibirsk region (81.2% in pol sequences) and is transmitted both among injecting drug users and by heterosexual contact. Similarity searches with database sequences combined with phylogenetic analyses show that CRF63-02A1 is circulating in East Kazakhstan and the Eastern area of Russia bordering China. The analyses of near full-length genome sequences show that its mosaic structure is more complex than reported, with 18 breakpoints. The tMRCA of CRF63-02A1 was estimated around 2006, with exponential growth in 2008-2009 and subsequent stabilization. These results provide new insights into the molecular epidemiology, phylogeny, and phylodynamics of CRF63-02A1.
机译:俄罗斯的HIV-1流行主要是前苏联的A亚型(AFSU)变异,但该国仍在传播其他遗传形式。一种是最近描述的CRF63-02A1,它源自在中亚传播的CRF02-AG变体与A FSU之间的重组,该FSU已在西伯利亚的新西伯利亚地区传播。在这里,我们系统地分析了2013年收集的来自新西伯利亚地区的24个HIV-1样本的pol和env片段,并对三个新的近乎全长基因组CRF63-02A1序列进行了表征,并估计了最近的共同祖先(tMRCA)的时间贝叶斯方法分析CRF63-02A1的人口增长情况。分析表明,CRF63-02A1在新西伯利亚地区(pol序列中占81.2%)高度占优势,并且在注射吸毒者之间和通过异性接触而传播。利用数据库序列进行的相似性搜索以及系统发育分析表明,CRF63-02A1在哈萨克斯坦东部和与中国接壤的俄罗斯东部地区流通。对近乎全长的基因组序列的分析表明,其镶嵌结构比报道的更为复杂,具有18个断点。 CRF63-02A1的tMRCA估计在2006年左右,在2008-2009年呈指数增长,随后稳定下来。这些结果为CRF63-02A1的分子流行病学,系统发育和系统动力学提供了新的见解。

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