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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Measles virus genetic evolution throughout an imported epidemic outbreak in a highly vaccinated population
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Measles virus genetic evolution throughout an imported epidemic outbreak in a highly vaccinated population

机译:在高度接种疫苗的人群中,从一次传入的流行病暴发中,麻疹病毒的遗传进化

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Measles virus circulates endemically in African and Asian large urban populations, causing outbreaks worldwide in populations with up-to-95% immune protection. We studied the natural genetic variability of genotype B3.1 in a population with 95% vaccine coverage throughout an imported six month measles outbreak. From first pass viral isolates of 47 patients we performed direct sequencing of genomic cDNA. Whilst no variation from index case sequence occurred in the Nucleocapsid gene hyper-variable carboxy end, in the Hemagglutinin gene, main target for neutralizing antibodies, we observed gradual nucleotide divergence from index case along the outbreak (0% to 0.380%, average 0.138%) with the emergence of transient and persistent non-synonymous and synonymous mutations. Little or no variation was observed between the index and last outbreak cases in Phosphoprotein, Nucleocapsid, Matrix and Fusion genes. Most of the H non-synonymous mutations were mapped on the protein surface near antigenic and receptors binding sites. We estimated a MV-Hemagglutinin nucleotide substitution rate of 7.28 x 10(-6) substitutions/site/day by a Bayesian phylogenetic analysis. The dN/dS analysis did not suggest significant immune or other selective pressures on the H gene during the outbreak. These results emphasize the usefulness of MV-H sequence analysis in measles epidemiological surveillance and elimination programs, and in detection of potentially emergence of measles virus neutralization-resistant mutants. (C) 2014 Elsevier B.V. All rights reserved.
机译:麻疹病毒在非洲和亚洲的大城市人群中流行,在全世界范围内爆发具有高达95%免疫保护的人群。我们研究了在整个进口的六个月麻疹暴发期间疫苗覆盖率达到95%的人群中B3.1基因型的自然遗传变异性。从47例患者的首次通过病毒分离物中,我们进行了基因组cDNA的直接测序。尽管在核中毒基因的高变羧基末端没有发生索引病例序列的变化,但在血凝素基因(中和抗体的主要靶标)中,我们观察到在爆发期间从索引病例中核苷酸逐渐出现差异(0%至0.380%,平均0.138%) )的出现,并出现了短暂且持续的非同义和同义突变。磷酸蛋白,核衣壳蛋白,基质和融合基因在指数暴发和最后一次暴发之间几乎没有变化。大多数H非同义突变被定位在蛋白质表面的抗原和受体结合位点附近。我们通过贝叶斯系统发育分析估计MV-血凝素核苷酸取代率为7.28 x 10(-6)取代/位点/天。 dN / dS分析未显示爆发期间H基因有明显的免疫压力或其他选择性压力。这些结果强调了MV-H序列分析在麻疹流行病学监测和消除计划中以及在检测可能出现的麻疹病毒中和抗性突变体中的有用性。 (C)2014 Elsevier B.V.保留所有权利。

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