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MiR-375 Has Contrasting Effects on Newcastle Disease Virus Growth Depending on the Target Gene

MicroRNAs regulate post-transcriptional gene expression via either translational repression or mRNA degradation. They have important roles in both viral infection and host anti-infection processes. We discovered that the miR-375 is significantly upregulated in Newcastle disease virus (NDV)-infected...

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Detalles Bibliográficos
Autores principales: Wang, Xinglong, Jia, Yanqing, Wang, Xiangwei, Wang, Chongyang, Lv, Changjie, Li, Xiaoqin, Chu, Zhili, Han, Qingsong, Xiao, Sa, Zhang, Shuxia, Yang, Zengqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329920/
https://www.ncbi.nlm.nih.gov/pubmed/30662346
http://dx.doi.org/10.7150/ijbs.25106
Descripción
Sumario:MicroRNAs regulate post-transcriptional gene expression via either translational repression or mRNA degradation. They have important roles in both viral infection and host anti-infection processes. We discovered that the miR-375 is significantly upregulated in Newcastle disease virus (NDV)-infected chicken embryonic visceral tissues using a small RNA sequencing approach. Further research revealed that the overexpression of miR-375 markedly decreases the replication of the velogenic NDV F48E9 and the lentogenic NDV La Sota by targeting the M gene of NDV in DF-1 cells. Interestingly, miR-375 has another target, ELAVL4, which regulates chicken fibrocyte cell cycle progression and decreases NDV proliferation. In addition, miR-375 can influence bystander cells by its secretion in culture medium. Our results indicated that miR-375 is an inhibitor of NDV, but can also enhance NDV growth by reducing the expression of its target ELAVL4. These results emphasize the complex roles of microRNAs in the regulation of viral infections.