| Literature DB >> 33626545 |
Yi Wang1,2, Zhiting Huo1,2, Quanshi Lin1,2, Yuxia Lin1,2, Cancan Chen3, Yanxia Huang1,2, Changbai Huang1,2, Junsong Zhang4, Junfang He1,2, Chao Liu1,5, Ping Zhang6,7.
Abstract
Expression of host noncoding RNAs and coding mRNAs is significantly altered by viral infection. In the current study, we screened the transcriptional profile of human lung epithelial A549 cells infected with Zika virus (ZIKV) by microarray assay. Seventy-nine long noncoding RNAs (lncRNAs) and 140 mRNAs were differentially expressed (DE). The bioinformatics analysis revealed that the mRNAs adjacent to the DE lncRNAs were closely related to the host responses to viral infection. We selected 7 lncRNAs from the top 50 hits for validation. The quantitative real-time PCR data confirmed that expression of selected lncRNAs was induced by ZIKV infection. Moreover, the expression of 7 lncRNAs was induced by infection of dengue virus, Japanese encephalitis virus, or vesicular stomatitis virus, or by treatment of poly(I:C) and IFN-β. Furthermore, loss of innate immune adaptor IPS-1 or receptor IFNAR1 resulted in lower induction levels of several lncRNAs by ZIKV. Overexpression of 3 lncRNAs (RPL27-OT1, OASL-IT1, and REC8-OT3) reduced the virus yields of ZIKV. Knockout of OASL-IT1 significantly enhanced ZIKV replication. In OASL-IT1 knockout cells, the levels of interferons (IFNs) and the activation of 3 innate immune signaling pathways triggered by ZIKV were dramatically reduced. Collectively, our work found a positive feedback loop in the IFN system, in which IFNs and OASL-IT1 regulate each other, thereby promoting establishment of antiviral defense.Entities:
Keywords: Innate immunity; Interferon; Interferon-stimulated gene; Long noncoding RNA; Zika virus
Year: 2021 PMID: 33626545 DOI: 10.1159/000513606
Source DB: PubMed Journal: J Innate Immun ISSN: 1662-811X Impact factor: 7.349