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New mutational trends in the HA protein of 2009 H1N1 pandemic influenza virus from May 2010 to February 2011

机译:2010年5月至2011年2月2009 H1N1大流行性流感病毒HA蛋白的新突变趋势

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摘要

As we enter the year of 2011, the 2009 H1N1 pandemic influenza virus is in the news again. At least 20 people have died of this virus in China since the beginning of 2011 and it is now the predominant flu strain in the country. Although this novel virus was quite stable during its run in the flu season of 2009-2010, a genetic variant of this virus was found in Singapore in early 2010, and then in Australia and New Zealand during their 2010 winter influenza season. Several critical mutations in the HA protein of this variant were uncovered in the strains collected from January 2010 to April 2010. Moreover, a structural homology model of HA from the A/Brisbane/10/2010(H1N1) strain was made based on the structure of A/California/04/2009 (H1N1). The purpose of this study was to investigate mutations in the HA protein of 2009 H1N1 from sequence data collected worldwide from May 2010 to February 2011. A fundamental problem in bioinformatics and biology is to find the similar gene sequences for a given gene sequence of interest. Here we proposed the inverse problem, i.e., finding the exemplars from a group of related gene sequences. With a clustering algorithm affinity propagation, six exemplars of the HA sequences were identified to represent six clusters. One of the clusters contained strain A/Brisbane/12/2010(H1N1) that only differed from A/Brisbane/10/2010 in the HA sequence at position 449. Based on the sequence identity of the six exemplars, nine mutations in HA were located that could be used to distinguish these six clusters. Finally, we discovered the change of correlation patterns for the HA and NA of 2009 H1N1 as a result of the HA receptor binding specificity switch, revealing the balanced interplay between these two surface proteins of the virus.
机译:随着我们进入2011年,2009 H1N1大流行性流感病毒再次成为新闻。自2011年初以来,在中国至少有20人死于该病毒,现在它已成为该国主要的流感病毒株。尽管这种新型病毒在2009-2010年流感季节运行期间相当稳定,但在2010年初在新加坡发现了这种病毒的遗传变异,然后在2010年冬季流感季节在澳大利亚和新西兰发现了这种病毒的遗传变异。从2010年1月至2010年4月收集的菌株中未发现该变体的HA蛋白中的几个关键突变。此外,根据结构构建了A / Brisbane / 10/2010(H1N1)菌株的HA结构同源模型。 A / California / 04/2009(H1N1)。这项研究的目的是从2010年5月至2011年2月在全球范围内收集的序列数据调查2009 H1N1的HA蛋白中的突变。生物信息学和生物学的一个基本问题是为给定的目标基因序列寻找相似的基因序列。在这里,我们提出了反问题,即从一组相关的基因序列中找到示例。利用聚类算法亲和力传播,确定了六个HA序列示例来代表六个聚类。其中一个簇包含菌株A / Brisbane / 12/2010(H1N1),在位置449处的HA序列仅与A / Brisbane / 10/2010不同。根据六个示例的序列同一性,HA中有9个突变可以用来区分这六个集群的位置。最后,我们发现2009年H1N1病毒的HA和NA的相关模式发生了变化,这是由于HA受体结合特异性的改变所致,揭示了这两种表面蛋白之间平衡的相互作用。

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