tetano
Editor, Senior Moderator
Virol J. 2019 Nov 12;16(1):135. doi: 10.1186/s12985-019-1227-4. [h=1]Mouse-adapted H9N2 avian influenza virus causes systemic infection in mice.[/h]
Hu Z[SUP]1[/SUP], Zhang Y[SUP]1,[/SUP][SUP]2[/SUP], Wang Z[SUP]1[/SUP], Wang J[SUP]1[/SUP], Tong Q[SUP]1[/SUP], Wang M[SUP]1[/SUP], Sun H[SUP]1[/SUP], Pu J[SUP]1[/SUP], Liu C[SUP]2[/SUP], Liu J[SUP]3[/SUP], Sun Y[SUP]4[/SUP].
[h=3]Author information[/h] 1 Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. 2 Beijing Huadu Yukou Poultry Industry Co. Ltd., Beijing, 101206, China. 3 Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. ljh@cau.edu.cn. 4 Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. sypcau@163.com.
[h=3]Abstract[/h] [h=4]BACKGROUND:[/h] H9N2 influenza viruses continuously circulate in multiple avian species and are repeatedly transmitted to humans, posing a significant threat to public health. To investigate the adaptation ability of H9N2 avian influenza viruses (AIVs) to mammals and the mutations related to the host switch events, we serially passaged in mice two H9N2 viruses of different HA lineages - A/Quail/Hong Kong/G1/97 (G1) of the G1-like lineage and A/chicken/Shandong/ZB/2007 (ZB) of the BJ/94-like lineage -and generated two mouse-adapted H9N2 viruses (G1-MA and ZB-MA) that possessed significantly higher virulence than the wide-type viruses.
[h=4]FINDING:[/h] ZB-MA replicated systemically in mice. Genomic sequence alignment revealed 10 amino acid mutations coded by 4 different gene segments (PB2, PA, HA, and M) in G1-MA compared with the G1 virus and 23 amino acid mutations in 5 gene segments (PB1, PA, HA, M, and NS) in ZB-MA compared to ZB virus, indicating that the mutations in the polymerase, HA, M, and NS genes play critical roles in the adaptation of H9N2 AIVs to mammals, especially, the mutations of M1-Q198H and M1-A239T were shared in G1-MA and ZB-MA viruses. Additionally, several substitutions showed a higher frequency in human influenza viruses compared with avian viruses.
[h=4]CONCLUSIONS:[/h] Different lineages of H9N2 could adapt well in mice and some viruses could gain the ability to replicate systemically and become neurovirulent. Thus, it is essential to pay attention to the mammalian adaptive evolution of the H9N2 virus.
[h=4]KEYWORDS:[/h] Adaption; H9N2 avian influenza virus; Mice; Mutation
PMID: 31718675 DOI: 10.1186/s12985-019-1227-4
Hu Z[SUP]1[/SUP], Zhang Y[SUP]1,[/SUP][SUP]2[/SUP], Wang Z[SUP]1[/SUP], Wang J[SUP]1[/SUP], Tong Q[SUP]1[/SUP], Wang M[SUP]1[/SUP], Sun H[SUP]1[/SUP], Pu J[SUP]1[/SUP], Liu C[SUP]2[/SUP], Liu J[SUP]3[/SUP], Sun Y[SUP]4[/SUP].
[h=3]Author information[/h] 1 Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. 2 Beijing Huadu Yukou Poultry Industry Co. Ltd., Beijing, 101206, China. 3 Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. ljh@cau.edu.cn. 4 Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. sypcau@163.com.
[h=3]Abstract[/h] [h=4]BACKGROUND:[/h] H9N2 influenza viruses continuously circulate in multiple avian species and are repeatedly transmitted to humans, posing a significant threat to public health. To investigate the adaptation ability of H9N2 avian influenza viruses (AIVs) to mammals and the mutations related to the host switch events, we serially passaged in mice two H9N2 viruses of different HA lineages - A/Quail/Hong Kong/G1/97 (G1) of the G1-like lineage and A/chicken/Shandong/ZB/2007 (ZB) of the BJ/94-like lineage -and generated two mouse-adapted H9N2 viruses (G1-MA and ZB-MA) that possessed significantly higher virulence than the wide-type viruses.
[h=4]FINDING:[/h] ZB-MA replicated systemically in mice. Genomic sequence alignment revealed 10 amino acid mutations coded by 4 different gene segments (PB2, PA, HA, and M) in G1-MA compared with the G1 virus and 23 amino acid mutations in 5 gene segments (PB1, PA, HA, M, and NS) in ZB-MA compared to ZB virus, indicating that the mutations in the polymerase, HA, M, and NS genes play critical roles in the adaptation of H9N2 AIVs to mammals, especially, the mutations of M1-Q198H and M1-A239T were shared in G1-MA and ZB-MA viruses. Additionally, several substitutions showed a higher frequency in human influenza viruses compared with avian viruses.
[h=4]CONCLUSIONS:[/h] Different lineages of H9N2 could adapt well in mice and some viruses could gain the ability to replicate systemically and become neurovirulent. Thus, it is essential to pay attention to the mammalian adaptive evolution of the H9N2 virus.
[h=4]KEYWORDS:[/h] Adaption; H9N2 avian influenza virus; Mice; Mutation
PMID: 31718675 DOI: 10.1186/s12985-019-1227-4