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首页> 外文期刊>Virus Evolution >Whole genome analysis of local Kenyan and global sequences unravels the epidemiological and molecular evolutionary dynamics of RSV genotype ON1 strains
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Whole genome analysis of local Kenyan and global sequences unravels the epidemiological and molecular evolutionary dynamics of RSV genotype ON1 strains

机译:肯尼亚当地和全球序列的全基因组分析揭示了RSV基因型ON1菌株的流行病学和分子进化动力学

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摘要

The respiratory syncytial virus (RSV) group A variant with the 72-nucleotide duplication in the G gene, genotype ON1, was first detected in Kilifi in 2012 and has almost completely replaced circulating genotype GA2 strains. This replacement suggests some fitness advantage of ON1 over the GA2 viruses in Kilifi, and might be accompanied by important genomic substitutions in ON1 viruses. Close observation of such a new virus genotype introduction over time provides an opportunity to better understand the transmission and evolutionary dynamics of the pathogen. We have generated and analysed 184 RSV-A whole-genome sequences (WGSs) from Kilifi (Kenya) collected between 2011 and 2016, the first ON1 genomes from Africa and the largest collection globally from a single location. Phylogenetic analysis indicates that RSV-A circulation in this coastal Kenya location is characterized by multiple introductions of viral lineages from diverse origins but with varied success in local transmission. We identified signature amino acid substitutions between ON1 and GA2 viruses’ surface proteins (G and F), polymerase (L), and matrix M2-1 proteins, some of which were positively selected, and thereby provide an enhanced picture of RSV-A diversity. Furthermore, five of the eleven RSV open reading frames (ORFs) (G, F, L, N, and P) formed distinct phylogenetic clusters for the two genotypes. This might suggest that coding regions outside of the most frequently studied G ORF also play a role in the adaptation of RSV to host populations, with the alternative possibility that some of the substitutions are neutral and provide no selective advantage. Our analysis provides insight into the epidemiological processes that define RSV spread, highlights the genetic substitutions that characterize emerging strains, and demonstrates the utility of large-scale WGS in molecular epidemiological studies.
机译:呼吸道合胞病毒(RSV)A组变异体在G基因中有72个核苷酸重复,基因型为ON1,最早于2012年在基利菲发现,已几乎完全取代了循环基因型GA2菌株。这种替代表明ON1相对于Kilifi中的GA2病毒具有一定的适应性优势,并且可能伴随有ON1病毒中的重要基因组替代。随着时间的流逝,对这种新病毒基因型的密切观察为更好地了解病原体的传播和进化动力学提供了机会。我们已经生成并分析了2011年至2016年间从基利菲(肯尼亚)收集的184个RSV-A全基因组序列(WGS),这是来自非洲的首批ON1基因组,也是全球单个地点收集的最大RS1-A全基因组序列。系统发育分析表明,在肯尼亚沿海地区,RSV-A循环的特征是多次引入来自不同起源的病毒谱系,但在本地传播中取得了不同的成功。我们确定了ON1和GA2病毒的表面蛋白(G和F),聚合酶(L)和基质M2-1蛋白之间的标志性氨基酸取代,其中一些被积极选择,从而提供了RSV-A多样性的增强照片。此外,在11个RSV开放阅读框(ORF)中的5个(G,F,L,N和P)形成了两种基因型的独特系统发育簇。这可能表明,最常研究的G ORF之外的编码区在RSV适应宿主种群中也发挥了作用,另一些可能性是某些取代是中性的,没有选择优势。我们的分析提供了对定义RSV传播的流行病学过程的洞察力,突出了表征新兴菌株的遗传替代,并证明了大规模WGS在分子流行病学研究中的实用性。

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