文章摘要
Research on NS1 Proteins of Group 2 Tembusu Virus Inhibiting the Production of Duck Type I IFN
  
DOI:10.16768/j.issn.1004-874X.2024.07.014
Author NameAffiliation
HUANG Yunzhen, ZHANG Junqin, LI Linlin, DONG Jiawen, XIANG Yong, LIAO Ming, SUN Minhua (广东省农业科学院动物卫生研究所 / 农业农村部禽流感等家禽重大疾病防控重点实验室 / 广东省畜禽疫病防治研究重点实验室广东  广州  510640) 
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Abstract:
      【Objective】Tembusu virus (TMUV) disease is an important infectious disease in waterfowl.  In previous  studies, we found that in the early stages of TMUV infection in ducks, the viral copy number of group 2 TMUV in organs such as the liver, kidney, and brain were significantly higher than those of group 3 TMUV. The study aimed to explore whether group  2 TMUV NS proteins had different effects on the innate immune response of ducks compared with group 3 TMUV.【Method】 Taking the group 2 TMUV-JM strain and the group 3 TMUV-GX strain as  research subjects, we constructed the eukaryotic  expression plasmids of NS proteins of the two strains and compared the effects of the NS proteins on the RIG-I-induced  activity of the IFN-β (Type I) promoter by a dual-Luciferase reporter system. With the eukaryotic expression plasmids of the  constructed  recombinant chimeric NS1 proteins, we investigated the interaction  region between NS1 and the key molecules  of RIG-I signaling pathway by confocal laser scanning microscopy, co-IP and Western Blotting. By using the reverse genetic  system, we constructed NS1 recombinant chimeric TMUV to clarify the inhibitory effect of NS1 on the IFN-β in DEF cells  with TMUV infection.【Result】The study results showed that TMUV-JM NS1 could inhibit RIG-I-induced activation of the  IFN-β promoter, while TMUV-GX NS1 did not exhibit the inhibitory activity. Further studies revealed that the TMUV-JM NS1  inhibited the expression of type I IFN via targeting TBK1, and the NS1 255-352 aa was the functional region of the inhibitory  effect.  It was found that TMUV-JM NS1 did not interact with TBK1 directly, but  reduced the phosphorylation level of TBK1  indirectly, thereby suppressed the expression of type I IFN.【Conclusion】Based on the study results, we found that the group  2 TMUV NS1 has activity in inhibiting the RIG-I signaling pathway, identified the key activity region and targeted molecule of  its inhibitory pathway, and clarified that group 2 TMUV NS1 affected duck type I IFN production by indirectly inhibiting the  phosphorylation of TBK1.
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