Identification and Characterization of MicroRNAs in Snakehead Fish Cell Line upon Snakehead Fish Vesiculovirus Infection

被引:35
|
作者
Liu, Xiaodan [1 ,2 ]
Tu, Jiagang [1 ,2 ]
Yuan, Junfa [1 ,2 ]
Liu, Xueqin [1 ,2 ]
Zhao, Lijuan [1 ,2 ]
Dawar, Farman Ullah [1 ,3 ]
Khattak, Muhammad Nasir Khan [3 ]
Hegazy, Abeer M. [1 ,4 ]
Chen, Nan [1 ,2 ]
Vakharia, Vikram N. [5 ]
Lin, Li [1 ,2 ]
机构
[1] Huazhong Agr Univ, Coll Fisheries, Dept Aquat Anim Med, Wuhan 430070, Peoples R China
[2] Freshwater Aquaculture Collaborat Innovat Ctr Hub, Wuhan 430070, Peoples R China
[3] Hazara Univ, Dept Zool, Mansehra 21300, Khyber Pakhtoon, Pakistan
[4] Natl Water Res Ctr, Cent Lab Environm Qual Monitoring, Cairo 13621, Egypt
[5] Univ Maryland, Inst Marine & Environm Technol, Baltimore, MD 21202 USA
关键词
snakehead fish Vesiculovirus; SSN-1; cell; miRNA; deep sequencing; TRANSLATIONAL REPRESSION; VIRUS; EXPRESSION; RNA; REPLICATION; INFLUENZA; PATHOGENS;
D O I
10.3390/ijms17020154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) play important roles in mediating multiple biological processes in eukaryotes and are being increasingly studied to evaluate their roles associated with cellular changes following viral infection. Snakehead fish Vesiculovirus (SHVV) has caused mass mortality in snakehead fish during the past few years. To identify specific miRNAs involved in SHVV infection, we performed microRNA deep sequencing on a snakehead fish cell line (SSN-1) with or without SHVV infection. A total of 205 known miRNAs were identified when they were aligned with the known zebrafish miRNAs, and nine novel miRNAs were identified using MiRDeep2 software. Eighteen and 143 of the 205 known miRNAs were differentially expressed at three and 24 h post-infection (poi), respectively. From the differentially-expressed miRNAs, five were randomly selected to validate their expression profiles using quantitative reverse transcription polymerase chain reaction (qRT-PCR), and their expression profiles were consistent with the microRNA sequencing results. In addition, the target gene prediction of the SHVV genome was performed for the differentially-expressed host miRNAs, and a total of 10 and 58 differentially-expressed miRNAs were predicted to bind to the SHVV genome at three and 24 h poi, respectively. The effects of three selected miRNAs (miR-130-5p, miR-214 and miR-216b) on SHVV multiplication were evaluated using their mimics and inhibitors via qRT-PCR and Western blotting. The results showed that all three miRNAs were able to inhibit the multiplication of SHVV; whereas the mechanisms underlying the SHVV multiplication inhibited by the specific miRNAs need to be further characterized in the future.
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页数:11
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