Wang Sheng-Fan, Su Ming-Wei, Tseng Sung-Pin, Li Ming-Chun, Tsao Ching-Han, Huang Szu-Wei, Chu Woei-Chyn, Liu Wu-Tse, Chen Yi-Ming Arthur, Huang Jason C
Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung, Taiwan; AIDS Prevention and Research Center, National Yang-Ming University, Taipei, Taiwan; Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan; Center for Infectious Disease and Cancer Research, Kaohsiung Medical University, Kaohsiung, Taiwan.
Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan; Institute of Biomedical Engineering, National Yang-Ming University, Taipei, Taiwan.
J Microbiol Immunol Infect. 2016 Aug;49(4):477-86. doi: 10.1016/j.jmii.2014.08.011. Epub 2014 Oct 31.
The swine-origin influenza A (H1N1) virus (S-OIV) has come to the forefront since 2009 and was identified as a new reassortant strain. The hemagglutinin (HA) glycoprotein mediates virus binding, contains antigenic regions recognized by neutralizing antibodies, and is associated with viral cross-species infection and adaption. The comparison study of codon usage preferences in influenza viral genomes was less extensive. In this study, we used codon usage pattern analyses to validate the adaption and origins of S-OIV.
Codon usage pattern was used to estimate the host adaption of S-OIVs. Phylogenetic analysis of the HA gene was conducted to understand the phylogeny of H1N1 viruses isolated from different hosts. Amino acid signature pattern on antigenic sites of HA was analyzed to understand the antigenic characteristics.
Results of phylogenetic analyses of HA gene indicate that S-OIVs group in identical clusters. The synonymous codon usage pattern analyses indicate that the effective number of codons versus GC content at the third codon position in the HA1 gene slightly differ from those in swine H1N1 and gradually adapted to human. Our data indicate that S-OIV evolution occurred according to positive selection within these antigenic regions. A comparison of antigenic site amino acids reveals similar signature patterns between S-OIV and 1918 human influenza strains.
This study proposes a new and effective way to gain a better understanding of the features of the S-OIV genome and evolutionary processes based on the codon usage pattern. It is useful to trace influenza viral origins and cross-species virus transmission.
自2009年以来,甲型H1N1流感病毒(S-OIV)已成为关注焦点,并被确定为一种新的重配毒株。血凝素(HA)糖蛋白介导病毒结合,包含可被中和抗体识别的抗原区域,且与病毒跨物种感染和适应有关。对流感病毒基因组密码子使用偏好的比较研究较少。在本研究中,我们使用密码子使用模式分析来验证S-OIV的适应性和起源。
使用密码子使用模式来估计S-OIV的宿主适应性。对HA基因进行系统发育分析,以了解从不同宿主分离的H1N1病毒的系统发育。分析HA抗原位点上的氨基酸特征模式,以了解抗原特性。
HA基因的系统发育分析结果表明,S-OIV聚集在相同的簇中。同义密码子使用模式分析表明,HA1基因中密码子的有效数量与第三密码子位置的GC含量与猪H1N1中的略有不同,并逐渐适应人类。我们的数据表明,S-OIV在这些抗原区域内根据正选择发生进化。抗原位点氨基酸的比较揭示了S-OIV与1918年人类流感毒株之间相似的特征模式。
本研究提出了一种新的有效方法,可基于密码子使用模式更好地理解S-OIV基因组的特征和进化过程。这对于追踪流感病毒的起源和跨物种病毒传播很有用。