Karnbunchob Nipawit, Omori Ryosuke, Tessmer Heidi L, Ito Kimihito
Division of Bioinformatics, Research Center for Zoonosis Control, Hokkaido University Sapporo, Japan.
Division of Bioinformatics, Research Center for Zoonosis Control, Hokkaido UniversitySapporo, Japan; Precursory Research for Embryonic Science and Technology, Japan Science and Technology AgencyKawaguchi, Japan.
Front Microbiol. 2016 Dec 26;7:2118. doi: 10.3389/fmicb.2016.02118. eCollection 2016.
Human influenza pandemics have historically been caused by reassortant influenza A viruses using genes from human and avian viruses. This genetic reassortment between human and avian viruses has been known to occur in swine during viral circulation, as swine are capable of circulating both avian and human viruses. Therefore, avian-to-swine transmission of viruses plays an important role in the emergence of new pandemic strains. The amino acids at several positions on PB2, PB1, and PA are known to determine the host range of influenza A viruses. In this paper, we track viral transmission between avian and swine to investigate the evolution on polymerase genes associated with their hosts. We traced viral transmissions between avian and swine hosts by using nucleotide sequences of avian viruses and swine viruses registered in the NCBI GenBank. Using BLAST and the reciprocal best hits technique, we found 32, 33, and 30 pairs of avian and swine nucleotide sequences that may be associated with avian-to-swine transmissions for PB2, PB1, and PA genes, respectively. Then, we examined the amino acid substitutions involved in these sporadic transmissions. On average, avian-to-swine transmission pairs had 5.47, 3.73, and 5.13 amino acid substitutions on PB2, PB1, and PA, respectively. However, amino acid substitutions were distributed over the positions, and few positions showed common substitutions in the multiple transmission events. Statistical tests on the number of repeated amino acid substitutions suggested that no specific positions on PB2 and PA may be required for avian viruses to infect swine. We also found that avian viruses that transmitted to swine tend to process I478V substitutions on PB2 before interspecies transmission events. Furthermore, most mutations occurred after the interspecies transmissions, possibly due to selective viral adaptation to swine.
从历史上看,人类流感大流行是由甲型流感病毒重配体引起的,这些病毒利用了来自人类和禽流感病毒的基因。已知人类和禽流感病毒之间的这种基因重配会在病毒传播期间在猪体内发生,因为猪能够传播禽流感病毒和人类流感病毒。因此,病毒从禽到猪的传播在新的大流行毒株出现过程中起着重要作用。已知PB2、PB1和PA上几个位置的氨基酸决定了甲型流感病毒的宿主范围。在本文中,我们追踪禽和猪之间的病毒传播,以研究与它们宿主相关的聚合酶基因的进化。我们通过使用NCBI基因库中登记的禽流感病毒和猪流感病毒的核苷酸序列,追踪了禽和猪宿主之间的病毒传播。利用BLAST和相互最佳匹配技术,我们分别发现了32、33和30对可能与PB2、PB1和PA基因从禽到猪传播相关的禽流感病毒和猪流感病毒核苷酸序列。然后,我们检查了这些零星传播中涉及的氨基酸替换。平均而言,从禽到猪的传播对在PB2、PB1和PA上分别有5.47、3.73和5.13个氨基酸替换。然而,氨基酸替换分布在各个位置,在多个传播事件中很少有位置显示出常见的替换。对重复氨基酸替换数量的统计测试表明,禽流感病毒感染猪可能不需要PB2和PA上的特定位置。我们还发现,传播到猪的禽流感病毒在种间传播事件之前往往在PB2上发生I478V替换。此外,大多数突变发生在种间传播之后,这可能是由于病毒对猪的选择性适应。