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MiR-214 inhibits snakehead vesiculovirus (SHVV) replication by targeting host GS.
- Source :
-
Fish & shellfish immunology [Fish Shellfish Immunol] 2019 Jan; Vol. 84, pp. 299-303. Date of Electronic Publication: 2018 Oct 09. - Publication Year :
- 2019
-
Abstract
- MicroRNAs (miRNAs) are small noncoding RNAs that have been reported to play important roles in virus replication. Snakehead vesiculovirus (SHVV) is a new rhabdovirus isolated from diseased hybrid snakehead and has caused heavy economical losses in cultured snakehead fish in China. Our previous study has revealed that miR-214 inhibited SHVV replication, but the underline mechanism was not completely understood. In this study, glycogen synthase (GS) gene was identified as a target gene of miR-214. Overexpression of miR-214 reduced cellular GS gene expression. Knockdown of GS by siRNA, similar to the overexpression of miR-214, inhibited SHVV replication. Moreover, we found that siGS-mediated inhibition of SHVV replication could be restored by reducing cellular miR-214 level via using miR-214 inhibitor, indicating that miR-214 inhibited SHVV replication at least partially via targeting GS. This study provided information for understanding the molecular mechanism of SHVV pathogenicity and a potential antiviral strategy against SHVV infection.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Fish Diseases virology
Fish Proteins metabolism
Glycogen Synthase metabolism
MicroRNAs metabolism
RNA, Viral metabolism
Rhabdoviridae Infections physiopathology
Rhabdoviridae Infections virology
Vesiculovirus genetics
Vesiculovirus physiology
Fish Diseases physiopathology
Fish Proteins genetics
Glycogen Synthase genetics
MicroRNAs genetics
Perciformes
RNA, Viral genetics
Rhabdoviridae Infections veterinary
Subjects
Details
- Language :
- English
- ISSN :
- 1095-9947
- Volume :
- 84
- Database :
- MEDLINE
- Journal :
- Fish & shellfish immunology
- Publication Type :
- Academic Journal
- Accession number :
- 30308292
- Full Text :
- https://doi.org/10.1016/j.fsi.2018.10.028