生物
传染性支气管炎病毒
抗原呈递
病毒学
抗原
鸡传染性支气管炎病毒
树突状细胞
病毒
冠状病毒科
分泌物
免疫系统
微生物学
免疫学
T细胞
2019年冠状病毒病(COVID-19)
医学
传染病(医学专业)
病理
疾病
生物化学
作者
Jinjiao Zuo,Yanan Cao,Zhisheng Wang,Abid Ullah Shah,Wenlei Wang,Chen Dai,Mingjia Chen,Jian Lin,Qian Yang
出处
期刊:Genomics
[Elsevier]
日期:2021-04-15
卷期号:113 (4): 1719-1732
被引量:4
标识
DOI:10.1016/j.ygeno.2021.04.027
摘要
Dendritic cells are first guard to defend avian infectious bronchitis virus (IBV) infection and invasion. While IBV always suppress dendritic cells and escape the degradation and presentation, which might help viruses to transfer and migrant. Initially, we compared two IBV's function in activating avian bone marrow dendritic cells (BMDCs) and found that both IBV (QX and M41) did not significantly increase surface marker of avian BMDCs. Moreover, a significant decrease of m6A modification level in mRNA, but an increased in the ut RNA were observed in avian BMDCs upon the prevalent IBV (QX) infection. Further study found that both non-structural protein 7 (NSP7) and NSP16 inhibited the maturation and cytokines secretion of BMDCs, as well as their antigen-presentation ability. Lastly, we found that gga-miR21, induced by both NSP7 and NSP16, inhibited the antigen presentation of avian BMDCs. Taken together, our results illustrated how IBV inhibited the antigen-presentation of avian DCs.
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