Marek's Disease Virus Cluster 3 miRNAs Restrict Virus' Early Cytolytic Replication and Pathogenesis

被引:11
|
作者
Liao, Yifei [1 ]
Zhuang, Guoqing [1 ,2 ]
Sun, Aijun [1 ,2 ]
Khan, Owais A. [1 ,3 ]
Lupiani, Blanca [1 ]
Reddy, Sanjay M. [1 ]
机构
[1] Texas A&M Univ, Coll Vet Med & Biomed Sci, Dept Vet Pathobiol, College Stn, TX 77843 USA
[2] Henan Agr Univ, Coll Anim Sci & Vet Med, Zhengzhou 450002, Peoples R China
[3] Texas A&M Univ, Texas A&M Vet Med Diagnost Lab, Canyon, TX 79016 USA
来源
VIRUSES-BASEL | 2020年 / 12卷 / 11期
关键词
Marek’ s disease virus; miRNA; replication; lymphoid organ atrophy; pathogenesis; MICRORNA CLUSTER; GENE; IDENTIFICATION; INFECTION; ATTENUATION; EXPRESSION; PATHOTYPE; DELETION; ENCODES; TARGETS;
D O I
10.3390/v12111317
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Herpesvirus-encoded microRNAs (miRNAs) have been discovered in infected cells; however, lack of a suitable animal model has hampered functional analyses of viral miRNAs in vivo. Marek's disease virus (MDV) (Gallid alphaherpesvirus 2, GaHV-2) genome contains 14 miRNA precursors, which encode 26 mature miRNAs, grouped into three clusters. In this study, the role of MDV-encoded cluster 3 miRNAs, also known as mdv1-miR-M8-M10, in pathogenesis was evaluated in chickens, the natural host of MDV. Our results show that deletion of cluster 3 miRNAs did not affect virus replication and plaque size in cell culture, but increased early cytolytic replication of MDV in chickens. We also observed that deletion of cluster 3 miRNAs resulted in significantly higher virus reactivation from peripheral blood lymphocytes. In addition, pathogenesis studies showed that deletion of cluster 3 miRNAs resulted in more severe atrophy of lymphoid organs and reduced mean death time, but did not affect the incidence of MDV-associated visceral tumors. We confirmed these results by generating a cluster 3 miRNA revertant virus in which the parental MDV phenotype was restored. To the best of our knowledge, our study provides the first evidence that MDV cluster 3 miRNAs play an important role in modulating MDV pathogenesis.
引用
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页数:12
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