Marek's disease virus encoded miR-M6 and miR-M10 are dispensable for virus replication and pathogenesis in chickens
文献类型: 外文期刊
第一作者: Yang, Shuaikang
作者: Yang, Shuaikang;Zhang, Shuai;Lu, Wenlong;Jin, Jiaxin;Sun, Aijun;Zhuang, Guoqing;Yang, Shuaikang;Zhang, Shuai;Lu, Wenlong;Jin, Jiaxin;Sun, Aijun;Zhuang, Guoqing;Liao, Yifei;Teng, Man;Chai, Shujun;Luo, Jun;Zhang, Gaiping;Teng, Man;Chai, Shujun;Luo, Jun;Zhang, Gaiping;Teng, Man;Luo, Jun;Zhang, Gaiping;Zhang, Gaiping
作者机构:
关键词: MiRNAs; miR-M6; miR-M10; Virus replication; Pathogenesis
期刊名称:VETERINARY MICROBIOLOGY ( 影响因子:3.293; 五年影响因子:3.599 )
ISSN: 0378-1135
年卷期: 2021 年 262 卷
页码:
收录情况: SCI
摘要: MicroRNAs (miRNAs) are a class of approximately 22 nucleotides long non-coding RNAs, and virus-encoded miRNAs play an important role in pathogenesis. Marek's disease virus (MDV) is an oncogenic avian alphaherpesvirus that causes immunosuppression and tumors in its natural host, chicken. In the MDV genome, 14 miRNA precursors and 26 mature miRNAs were identified, thus MDV has been used as a model to study the function of viral miRNAs in vivo. Recently, a cluster of miRNAs encoded by MDV, Cluster 3 miRNAs (miR-M8M10), has been shown to restrict early cytolytic replication and pathogenesis of MDV. In this study, we further analyzed the role of miR-M6 and miR-M10, members of cluster miR-M8-M10, in MDV replication and pathogenicity. We found that, compared to parental MDV, deletion of miR-M6-5p significantly enhanced the replication of MDV in cell culture, but not in chickens. The replication of miR-M6-5p deletion MDV was restored once the deleted sequences were re-inserted. Our results also showed that deletion of miR-M10-5p did not affect the replication of MDV in vitro and in vivo. In addition, our animal study results showed that deletion of miRM6- 5p or miR-M10-5p did not alter the pathogenesis of MDV. In conclusion, our study shows that both miR-M6 and miR-M10 are dispensable for MDV replication and pathogenesis in chickens, while also suggests a repressive role of miR-M6 in MDV replication in cell culture.
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