RNA sequencing reveals CircRNA expression profiles in chicken embryo fibroblasts infected with velogenic Newcastle disease virus

文献类型： 外文期刊

第一作者： Chen, Libin

作者： Chen, Libin;Ruan, Jiayu;Chen, Yiyi;Deng, Wenxuan;Lai, Jinyu;Fan, Lei;Cai, Juncheng;Lin, Qiuyan;Ren, Tao;Chen, Libin;Ruan, Jiayu;Chen, Yiyi;Deng, Wenxuan;Lai, Jinyu;Fan, Lei;Cai, Juncheng;Lin, Qiuyan;Ren, Tao;Chen, Libin;Ruan, Jiayu;Chen, Yiyi;Deng, Wenxuan;Lai, Jinyu;Fan, Lei;Cai, Juncheng;Lin, Qiuyan;Ren, Tao;Chen, Libin;Ruan, Jiayu;Chen, Yiyi;Deng, Wenxuan;Lai, Jinyu;Fan, Lei;Cai, Juncheng;Lin, Qiuyan;Ren, Tao;Ding, Chan;Xiang, Bin

作者机构：

关键词： chicken embryo fibroblasts; Newcastle disease virus; RNA sequencing; infection; circular RNA

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 an important avian pathogen prevalent worldwide; it has an extensive host range and seriously harms the poultry industry. Velogenic NDV strains exhibit high pathogenicity and mortality in chickens. Circular RNAs (circRNAs) are among the most abundant and conserved eukaryotic transcripts. They are part of the innate immunity and antiviral response. However, the relationship between circRNAs and NDV infection is unclear. MethodsIn this study, we used circRNA transcriptome sequencing to analyze the differences in circRNA expression profiles post velogenic NDV infection in chicken embryo fibroblasts (CEFs). 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 further predicted. Moreover, circ-EZH2 was selected to determine its effect on NDV infection in CEFs. ResultsNDV infection altered circRNA expression profiles in CEFs, and 86 significantly DE circRNAs were identified. GO and KEGG enrichment analyses revealed significant enrichment of DE circRNAs for metabolism-related pathways, such as lysine degradation, glutaminergic synapse, and alanine, aspartic-acid, and glutamic-acid metabolism. The circRNA- miRNA-mRNA interaction networks further demonstrated that CEFs might combat NDV infection by regulating metabolism through circRNA-targeted mRNAs and miRNAs. Furthermore, we verified that circ-EZH2 overexpression and knockdown inhibited and promoted NDV replication, respectively, indicating that circRNAs are involved in NDV replication. ConclusionsThese results demonstrate that CEFs exert antiviral responses by forming circRNAs, offering new insights into the mechanisms underlying NDV-host interactions.

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