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J Virol . Reassortment with dominant chicken H9N2 influenza virus contributed to the fifth H7N9 virus human epidemic

tetano

Editor, Senior Moderator
J Virol


. 2021 Mar 17;JVI.01578-20.
doi: 10.1128/JVI.01578-20. Online ahead of print.
Reassortment with dominant chicken H9N2 influenza virus contributed to the fifth H7N9 virus human epidemic


Juan Pu[SUP] 1 [/SUP], Yanbo Yin[SUP] 2 [/SUP], Jiyu Liu[SUP] 3 [/SUP], Xinyu Wang[SUP] 3 [/SUP], Yong Zhou[SUP] 3 [/SUP], Zejiang Wang[SUP] 3 [/SUP], Yipeng Sun[SUP] 3 [/SUP], Honglei Sun[SUP] 3 [/SUP], Fangtao Li[SUP] 3 [/SUP], Jingwei Song[SUP] 3 [/SUP], Runkang Qu[SUP] 3 [/SUP], Weihua Gao[SUP] 3 [/SUP], Dongdong Wang[SUP] 4 [/SUP], Zhen Wang[SUP] 3 [/SUP], Shijie Yan[SUP] 3 [/SUP], Mingyue Chen[SUP] 3 [/SUP], Jinfeng Zeng[SUP] 5 [/SUP], Zhimin Jiang[SUP] 3 [/SUP], Haoran Sun[SUP] 3 [/SUP], Yanan Zong[SUP] 3 [/SUP], Chenxi Wang[SUP] 3 [/SUP], Qi Tong[SUP] 3 [/SUP], Yuhai Bi[SUP] 6 [/SUP], Yinhua Huang[SUP] 7 [/SUP], Xiangjun Du[SUP] 5 [/SUP], Kin-Chow Chang[SUP] 8 [/SUP], Jinhua Liu[SUP] 1 [/SUP]



Affiliations

Abstract

H9N2 Avian influenza virus (AIV) is regarded as a principal donor of viral genes through reassortment to co-circulating influenza viruses that can result in zoonotic reassortants. Whether H9N2 virus can maintain sustained evolutionary impact on such reassortants is unclear. Since 2013, avian H7N9 virus had caused five sequential human epidemics in China; the fifth wave in 2016-2017 was by far the largest but the mechanistic explanation behind the scale of infection is not clear. Here, we found that, just prior to the fifth H7N9 virus epidemic, H9N2 viruses had phylogenetically mutated into new sub-clades, changed antigenicity and increased its prevalence in chickens vaccinated with existing H9N2 vaccines. In turn, the new H9N2 virus sub-clades of PB2 and PA genes, housing mammalian adaptive mutations, were reassorted into co-circulating H7N9 virus to create a novel dominant H7N9 virus genotype that was responsible for the fifth H7N9 virus epidemic. H9N2-derived PB2 and PA genes in H7N9 virus conferred enhanced polymerase activity in human cells at 33?C and 37?C, and increased viral replication in the upper and lower respiratory tracts of infected mice which could account for the sharp increase in human cases of H7N9 virus infection in the 2016-2017 epidemic. The role of H9N2 virus in the continual mutation of H7N9 virus highlights the public health significance of H9N2 virus in the generation of variant reassortants of increasing zoonotic potential.IMPORTANCEAvian H9N2 influenza virus, although primarily restricted to chicken populations, is a major threat to human public health by acting as a donor of variant viral genes through reassortment to co-circulating influenza viruses. We established that the high prevalence of evolving H9N2 virus in vaccinated flocks played a key role, as donor of new sub-clade PB2 and PA genes in the generation of a dominant H7N9 virus genotype (G72) with enhanced infectivity in humans during the 2016-2017 N7N9 virus epidemic. Our findings emphasize that the ongoing evolution of prevalent H9N2 virus in chickens is an important source, via reassortment, of mammalian adaptive genes for other influenza virus subtypes. Thus, close monitoring of prevalence and variants of H9N2 virus in chicken flocks is necessary in the detection of zoonotic mutations.
 
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