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  1. NTU Scholars
  2. 生物資源暨農學院
  3. 獸醫專業學院
  4. 獸醫學系
Please use this identifier to cite or link to this item: https://scholars.lib.ntu.edu.tw/handle/123456789/629724
Title: NS2 is a key determinant of compatibility in reassortant avian influenza virus with heterologous H7N9-derived NS segment
Authors: Liu, Yee Chen
Liao, Guan Ru
Tsai, April Y.
Tseng, Ching Yu
Kuan, Chih Ying
Tsai, Ruei Sheng
Albrecht, Randy A.
Kuo, Rei Lin
IVAN-CHEN CHENG 
Liang, Wan Ting
Ou, Shan Chia
Hsu, Wei-Li
Keywords: Avian influenza virus | H7N9 | Immune response | NS1 protein | NS2
Issue Date: 15-Jan-2023
Publisher: ELSEVIER
Journal Volume: 324
Source: Virus Research
Abstract: 
Influenza A viruses are common pathogens with high prevalence worldwide and potential for pandemic spread. While influenza A infections typically elicit robust cellular innate immune responses, the non-structural protein 1 (NS1) antagonizes host anti-viral responses and is critical for efficient virus replication and virulence. The avian influenza virus (AIV) H7N9 initially emerged in China in 2013 and has since crossed the avian-human barrier, causing severe disease in humans. To investigate the influence of the H7N9 NS gene (NS079) on viral replication and innate immune response, we generated several recombinant AIVs bearing various NS079 segments on the backbone of H6N1 (strain 0702). Intriguingly, the recombinant virus bearing the heterologous NS079 gene was highly attenuated compared with virus carrying the homologous NS gene (NS0702). Furthermore, we generated a NS079-0702R virus that expresses a chimeric NS gene in which part of the NS079 effector domain was replaced with the sequence from NS0702. The NS079-0702R virus exhibited significantly enhanced viral yield, approximately 100-fold more than virus bearing NS079. The high infection rate of NS079-0702R virus was reflected by strong induction of IFN and Mx expression in human A549 cells. Intriguingly, our in vitro comparative analysis suggested that the increased NS079-0702R infection capacity was independent of the ability of NS1 to interact with cellular partners, such as PKR and CPSF30. Since partial substitution of the effector domain from NS0702 altered the coding sequence of NS2, we further generated another recombinant virus with NS2 derived from H7N9. Surprisingly, the virus with H7N9-derived NS2 exhibited growth characteristics similar to NS079. Our data demonstrate that swapping NS2 components changes infection efficiency, suggesting a key role for NS2 as a determinant of viral compatibility upon reassortment. These findings warrant further investigation into the precise mechanisms by which NS2 contributes to viral replication and host immunity.1
URI: https://scholars.lib.ntu.edu.tw/handle/123456789/629724
ISSN: 01681702
DOI: 10.1016/j.virusres.2022.199028
Appears in Collections:獸醫學系

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