Circular RNAs are associated with the resistance to Newcastle disease virus infection in duck cells

文献类型： 外文期刊

第一作者： Fan, Lei

作者： Fan, Lei;Ren, Jinlian;Wang, Yinchu;Chen, Yiyi;Chen, Yichun;Chen, Libin;Lin, Qiuyan;Ren, Tao;Fan, Lei;Ren, Jinlian;Wang, Yinchu;Chen, Yiyi;Chen, Yichun;Chen, Libin;Lin, Qiuyan;Ren, Tao;Fan, Lei;Ren, Jinlian;Wang, Yinchu;Chen, Yiyi;Chen, Yichun;Chen, Libin;Lin, Qiuyan;Ren, Tao;Fan, Lei;Ren, Jinlian;Wang, Yinchu;Chen, Yiyi;Chen, Yichun;Chen, Libin;Lin, Qiuyan;Ren, Tao;Liao, Ming;Ding, Chan;Xiang, Bin

作者机构：

关键词： waterfowl; Newcastle disease virus; duck embryo fibroblasts; circular RNAs; antiviral response

期刊名称：FRONTIERS IN VETERINARY SCIENCE （ 影响因子：3.2； 五年影响因子：3.5 ）

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年卷期： 2023 年 10 卷

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收录情况： SCI

摘要： IntroductionNewcastle disease virus (NDV) is prevalent worldwide with an extensive host range. Among birds infected with velogenic NDV strains, chickens experience high pathogenicity and mortality, whereas ducks mostly experience mild symptoms or are asymptomatic. Ducks have a unique, innate immune system hypothesized to induce antiviral responses. Circular RNAs (circRNAs) are among the most abundant and conserved eukaryotic transcripts. These participate in innate immunity and host antiviral response progression.MethodsIn this study, circRNA expression profile differences post-NDV infection in duck embryo fibroblast (DEF) cells were analyzed using circRNA transcriptome sequencing. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were used to reveal significant enrichment of differentially expressed (DE) circRNAs. The circRNA-miRNA-mRNA interaction networks were used to predict the related functions of circRNAs. Moreover, circ-FBXW7 was selected to determine its effect on NDV infection in DEFs.ResultsNDV infection altered circRNA expression profiles in DEF cells, and 57 significantly differentially expressed circRNAs were identified post-NDV infection. DEF responded to NDV by forming circRNAs to regulate apoptosis-, cell growth-, and protein degradation-related pathways via GO and KEGG enrichment analyses. circRNA-miRNA-mRNA interaction networks demonstrated that DEF cells combat NDV infection by regulating cellular pathways or apoptosis through circRNA-targeted mRNAs and miRNAs. circ-FBXW7 overexpression and knockdown inhibited and promoted viral replication, respectively. DEF cells mainly regulated cell cycle alterations or altered cellular sensing to combat NDV infection.ConclusionThese results demonstrate that DEF cells exert antiviral responses by forming circRNAs, providing novel insights into waterfowl antiviral responses.

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