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Integrated analysis of viral miRNAs, mRNA and protein in the caudal fin cells of C. auratus gibelio with cyprinid herpesvirus 2 infection
Author(s) -
Luo Yang,
Yu Lu,
Feng Zizhao,
Chen Qikang,
Lu Liqun,
Zhang Qiya,
Xu Dan
Publication year - 2021
Publication title -
journal of fish diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.819
H-Index - 85
eISSN - 1365-2761
pISSN - 0140-7775
DOI - 10.1111/jfd.13289
Subject(s) - biology , gene , microbiology and biotechnology , virus , messenger rna , virology , real time polymerase chain reaction , viral protein , gene expression , transcriptome , complementary dna , microrna , crucian carp , genetics , fishery , fish <actinopterygii>
Cyprinid herpesvirus 2 (CyHV‐2), a member of the genus Cyprinivirus in the family Alloherpesviridae , has attracted worldwide attention because it causes severe disease and high mortality in crucian carp and goldfish. In this study, we focus on mRNA, protein and viral miRNA expression profiles in C. auratus gibelio caudal fin (GiCF) cells infected with CyHV‐2, using high‐throughput sequence techniques and TMT‐labelled analyses. The results revealed that 156 virus genes were differentially expressed during the infection. Among these differentially expressed genes, 7 viral genes were significantly up‐regulated and 28 were significantly down‐regulated at 96 hpi (hours post‐infection) vs 48 hpi. Besides, a total of 78 viral proteins, including a large number of membrane proteins and capsid proteins associated with the viral assembly, were successfully detected by using proteome analysis. Furthermore, a total of 225,143,474 raw reads were generated from cDNA library of CyHV‐2‐infected GiCF cells using high‐throughput sequencing technology. Following annotation and secondary structure prediction, 10 viral miRNAs were found as significantly modulated in CyHV‐2‐infected GiCF cells (2 down‐regulated and 8 up‐regulated). Finally, the CyHV‐2 genes ( orf19 , orf23 , orf118 , orf121 , orf127 ) targeted by the viral miRNA CyHV‐2‐KT‐635 identified in this study, were predicted and validated by quantitative reverse transcription polymerase chain reaction (qRT‐PCR), and the regulation of CyHV‐2‐KT‐635 on orf121 protein expression was verified by western blotting assay. Taken together, this study provides a valuable basis for further research on the expression of virus genes during CyHV‐2 replication and the molecular mechanisms by which miRNA may regulate CyHV‐2 virus.