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首页> 外文期刊>Journal of microbiology and biotechnology >Envelope proteins pertain with evolution and adaptive mechanism of the novel influenza A/H1N1 in humans
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Envelope proteins pertain with evolution and adaptive mechanism of the novel influenza A/H1N1 in humans

机译:信封蛋白与人类新型A / H1N1流感的进化和适应机制有关

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摘要

The novel swine-origin influenza A/H1N1 virus (S-OIV) first detected in April 2009 has been identified to transmit from humans to humans directly and is the cause of the currently emerged pandemic. In this study, nucleotide and deduced amino acid sequences of the hemagglutinin (HA) and neuraminidase (NA) of the S-OIV and other influenza A viruses were analyzed through bioinformatic tools for phylogenetic analysis, genetic recombination, and point mutation to investigate the emergence and adaptation of the S-OIV in humans. The phylogenetic analysis showed that the HA comes from triple reassortant influenza A/H1N2 and the NA from Eurasian swine influenza A/H1N1, indicating that HA and NA descend from different lineages during the genesis of the S-OIV. Recombination analysis nullified the possibility of occurrence of recombination in HA and NA, denoting the role of reassortment in the outbreak. Several conservative mutations were observed in the amino acid sequences of the HA and NA, and these mutated residues were identical in the S-OIV. The results reported herein suggest the notion that the recent pandemic is the result of reassortment of different genes from different lineages of two envelope proteins, HA and NA, which are responsible for the antigenic activity of the virus. This study further suggests that the adaptive capability of the S-OIV in humans is acquired by the unique mutations generated during emergence.
机译:2009年4月首次发现的新型猪源性A / H1N1流感病毒(S-OIV)已被确定可在人与人之间直接传播,并且是当前大流行的原因。在这项研究中,通过生物信息学工具对S-OIV和其他甲型流感病毒的血凝素(HA)和神经氨酸酶(NA)的核苷酸和推导的氨基酸序列进行了分析,以进行系统发育分析,基因重组和点突变,以研究出现的情况和S-OIV在人类中的适应性。系统发育分析表明,HA来源于三重重排流感A / H1N2,NA来自欧亚猪流感A / H1N1,表明HA和NA在S-OIV发生过程中来自不同谱系。重组分析消除了HA和NA中重组发生的可能性,表明重组在疾病暴发中的作用。在HA和NA的氨基酸序列中观察到几个保守突变,并且这些突变的残基在S-OIV中是相同的。本文报道的结果表明,最近的大流行是来自两个包膜蛋白HA和NA不同谱系的不同基因重排的结果,这两个包膜蛋白负责病毒的抗原活性。这项研究进一步表明,S-OIV在人体内的适应能力是通过出现时产生的独特突变获得的。

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