tetano
Editor, Senior Moderator
Front Microbiol
. 2020 Jul 22;11:1441.
doi: 10.3389/fmicb.2020.01441. eCollection 2020.
Internal Gene Cassette From a Human-Origin H7N9 Influenza Virus Promotes the Pathogenicity of H9N2 Avian Influenza Virus in Mice
Miaomiao Zhang[SUP] 1 2 [/SUP], Chen Zhao[SUP] 2 [/SUP], Hongjun Chen[SUP] 1 [/SUP], Qiaoyang Teng[SUP] 1 [/SUP], Lang Jiang[SUP] 2 [/SUP], Daobin Feng[SUP] 2 [/SUP], Xuesong Li[SUP] 1 [/SUP], Songhua Yuan[SUP] 2 [/SUP], Jianqing Xu[SUP] 2 [/SUP], Xiaoyan Zhang[SUP] 2 [/SUP], Zejun Li[SUP] 1 [/SUP]
Affiliations
Abstract
H9N2 avian influenza virus is one of the most widely circulating viruses in poultry and poses a huge potential threat to human health due to its frequent gene reassortment with other influenza viruses. In this study, we generated a series of H9N2-H7N9 reassortant viruses and examined their pathogenicity in a mouse model. We found that HA or combined HA and NA replacement on the H9N2 background led to no substantial change in the virus-induced pathogenicity, whereas H9N2 virus containing H7N9 internal genes had significantly higher virulence in comparison to the parental H9N2 virus. This increased pathogenicity is associated with enhanced viral replication both in mice and in MDCK cells. We further demonstrated that the viral ribonucleoprotein complex from H7N9 virus possessed higher activity than that from its H9N2 counterpart. Collectively, our data demonstrated that genetic compatibility between H9N2 and H7N9 viruses facilitated the reassortment between H7N9 and H9N2 viruses co-circulated in poultry and that internal gene replacement would convert H9N2 virus into a novel threat to human health.
Keywords: H7N9; H9N2; avian influenza; internal gene; pathogenicity.
. 2020 Jul 22;11:1441.
doi: 10.3389/fmicb.2020.01441. eCollection 2020.
Internal Gene Cassette From a Human-Origin H7N9 Influenza Virus Promotes the Pathogenicity of H9N2 Avian Influenza Virus in Mice
Miaomiao Zhang[SUP] 1 2 [/SUP], Chen Zhao[SUP] 2 [/SUP], Hongjun Chen[SUP] 1 [/SUP], Qiaoyang Teng[SUP] 1 [/SUP], Lang Jiang[SUP] 2 [/SUP], Daobin Feng[SUP] 2 [/SUP], Xuesong Li[SUP] 1 [/SUP], Songhua Yuan[SUP] 2 [/SUP], Jianqing Xu[SUP] 2 [/SUP], Xiaoyan Zhang[SUP] 2 [/SUP], Zejun Li[SUP] 1 [/SUP]
Affiliations
- PMID: 32793127
- PMCID: PMC7387514
- DOI: 10.3389/fmicb.2020.01441
Abstract
H9N2 avian influenza virus is one of the most widely circulating viruses in poultry and poses a huge potential threat to human health due to its frequent gene reassortment with other influenza viruses. In this study, we generated a series of H9N2-H7N9 reassortant viruses and examined their pathogenicity in a mouse model. We found that HA or combined HA and NA replacement on the H9N2 background led to no substantial change in the virus-induced pathogenicity, whereas H9N2 virus containing H7N9 internal genes had significantly higher virulence in comparison to the parental H9N2 virus. This increased pathogenicity is associated with enhanced viral replication both in mice and in MDCK cells. We further demonstrated that the viral ribonucleoprotein complex from H7N9 virus possessed higher activity than that from its H9N2 counterpart. Collectively, our data demonstrated that genetic compatibility between H9N2 and H7N9 viruses facilitated the reassortment between H7N9 and H9N2 viruses co-circulated in poultry and that internal gene replacement would convert H9N2 virus into a novel threat to human health.
Keywords: H7N9; H9N2; avian influenza; internal gene; pathogenicity.