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Characterization of duck tembusu virus NS2A membrane topology and functional residues in transmembrane domain-3 on viral proliferation

Authors :
Zhang, Wei
Zeng, Miao
Jiang, Bowen
Cheng, Yao
He, Yu
Wu, Zhen
Wang, Tao
Wang, Mingshu
Jia, Renyong
Zhu, Dekang
Liu, Mafeng
Zhao, Xinxin
Yang, Qiao
Wu, Ying
Zhang, Shaqiu
Huang, Juan
Ou, Xumin
Sun, Di
Merits, Andres
Cheng, Anchun
Chen, Shun
Source :
Poultry Science; December 2024, Vol. 103 Issue: 12
Publication Year :
2024

Abstract

Flavivirus nonstructural protein 2A (NS2A) is a small endoplasmic reticulum (ER)-resident, hydrophobic transmembrane protein that function in viral replication, virion assembly and evasion of the host immune response. Despite previous studies on the role of duck Tembusu virus (DTMUV) NS2A in inhibiting the host immune response, its membrane topology has not been clearly addressed (Zhang et al., 2020; Zhang et al., 2022). Here, we present the first report on the membrane topology model and functional characterization of DTMUV NS2A. Our findings demonstrate that DTMUV NS2A localizes to the endoplasmic reticulum (ER) and associates with viral double-stranded RNA, with a single segment (TMD3, amino acids 72 to 95) spanning the ER membrane. To better delineate the residues in NS2A-TMD3 related to viral properties, specific mutations were introduced to generate DTMUV replicons and infectious cDNA clones. Functional analysis indicates that L77, Q86 and L89 of NS2A are crucial for viral RNA synthesis, while residues M79 and F83 are crucial for the assembly or release of viral particles. Moreover, these mutations attenuated the virulence of DTMUV in vivo. Collectively, our results shed light on the relationship between the transmembrane of DTMUV NS2A and its functions in virus proliferation, providing insights for further understanding the molecular mechanisms of NS2A in the virus life cycle.

Details

Language :
English
ISSN :
00325791 and 15253171
Volume :
103
Issue :
12
Database :
Supplemental Index
Journal :
Poultry Science
Publication Type :
Periodical
Accession number :
ejs67679908
Full Text :
https://doi.org/10.1016/j.psj.2024.104423