Is a highly pathogenic avian influenza virus H5N1 fragment recombined in PB1 the key for the epidemic of the novel AIV H7N9 in China, 2013?

• Published in: International journal of infectious diseases Vol. 43; no. C; pp. 85 - 89
• Main Authors: Chen, Liang, Sun, Liqian, Li, Rui, Chen, Yue, Zhang, Zhijie, Xiong, Chenglong, Zhao, Genming, Jiang, Qingwu
• Format: Journal Article
• Language: English
• Published: Canada Elsevier Ltd 01.02.2016; Elsevier
• Subjects: Animals; Biological Evolution; China; China - epidemiology; Epidemics; Genome, Viral - genetics; H7N9; Humans; Infectious Disease; Influenza A Virus, H5N1 Subtype - genetics; Influenza A Virus, H5N1 Subtype - pathogenicity; Influenza A Virus, H7N9 Subtype - genetics; Influenza A Virus, H7N9 Subtype - pathogenicity; Influenza A Virus, H9N2 Subtype - genetics; Influenza A Virus, H9N2 Subtype - pathogenicity; Influenza virus; Influenza, Human - epidemiology; Influenza, Human - virology; Phylogeny; Pulmonary/Respiratory; Recombination; Recombination, Genetic; Viral Proteins - genetics; Virulence; Recombination; H7N9; Influenza virus; China
• ISSN: 1201-9712; 1878-3511; 1878-3511
• DOI: 10.1016/j.ijid.2016.01.002

•The characteristics of recombination, rather than reassortment, for each segment of the genome of a novel avian influenza virus (AIV) H7N9 were investigated comprehensively in this study, and the evolutionary histories of the identified recombined fragments were also traced.•A 291-nt fragment affiliated with a highly pathogenic avian influenza virus (HPAIV) H5N1 was recombinated into PB1 segment of the novel AIV H7N9 in China in 2013, at the 490-780 nt site might have been a pivotal factor for the high fatality rate of the latter. A novel avian influenza A H7N9 virus that infects humans was identified in China in 2013. This study is the first to comprehensively investigate the characteristics of genomic recombination, rather than reassortment, which has been the subject of investigation in previously reported studies. Novel avian influenza virus (AIV) H7N9 genome sequences were obtained from the NCBI Influenza Virus Sequence Database and the Global Initiative on Sharing Avian Influenza Database (GISAID) and a representative isolate was subjected to homogeneity analysis. A phylogenetic tree was constructed. Eight segments of the isolate were analyzed to identify segments with recombination events, the corresponding recombination fragments, and breakpoints. The evolutionary history of the recombined fragments was tracked by constructing phylogenetic trees of the recombination fragments. Among the eight segments of the novel AIV H7N9 analyzed, only the PB1 segment showed a marked recombination phenomenon, with 11 recombination events; these included five actual recombination events and six possible misalignment artifact recombination events. The most notable was the recombination of a 291-nucleotide (nt) fragment at the 490–780 nt site that was affiliated to a highly pathogenic avian influenza virus (HPAIV) H5N1 (A/tree sparrow/Thailand/VSMU-16-RBR/2005). The phylogenetic tree of the 291-nt recombination fragment on the PB1 segment showed that the novel AIV H7N9 had a close genetic relationship to H9N2 and H5N1. The novel AIV H7N9 might have reassorted its PB1 segment from H9N2 circulating in China, and this H9N2 PB1 might have been recombined into a highly pathogenic fragment from HPAIV H5N1, which could be the reason for the high fatality rate among patients with AIV H7N9 influenza.