Marek's disease virus encoded miR-M6 and miR-M10 are dispensable for virus replication and pathogenesis in chickens

生物 病毒 马立克氏病 发病机制 病毒复制 病毒学 小RNA 病毒病机 基因 遗传学 免疫学
作者
Shuaikang Yang,Yifei Liao,Shuai Zhang,Wenlong Lu,Jiaxin Jin,Man Teng,Shujun Chai,Jun Luo,Gaiping Zhang,Aijun Sun,Guoqing Zhuang
出处
期刊:Veterinary Microbiology [Elsevier BV]
卷期号:262: 109248-109248 被引量:8
标识
DOI:10.1016/j.vetmic.2021.109248
摘要

Abstract 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-M8-M10), 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 miR-M6−5p 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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