PUBLICATION
Proteomic analysis of cellular protein expression profiles in response to grass carp reovirus infection
- Authors
- Xu, D., Song, L., Wang, H., Xu, X., Wang, T., Lu, L.
- ID
- ZDB-PUB-150319-7
- Date
- 2015
- Source
- Fish & shellfish immunology 44(2): 515-24 (Journal)
- Registered Authors
- Wang, Hao
- Keywords
- CiG3BP1, CiTIA1, Grass carp reovirus, Stress Granule, proteomics
- MeSH Terms
-
- Animals
- Aquaculture
- Blotting, Western/veterinary
- Carps*
- Electrophoresis, Gel, Two-Dimensional/veterinary
- Fish Diseases/metabolism*
- Fish Diseases/microbiology*
- Gene Expression Profiling/veterinary
- Gene Expression Regulation/genetics*
- Proteome/genetics*
- Real-Time Polymerase Chain Reaction/veterinary
- Reoviridae Infections/metabolism
- Reoviridae Infections/veterinary*
- Reverse Transcriptase Polymerase Chain Reaction/veterinary
- Tandem Mass Spectrometry/veterinary
- PubMed
- 25783000 Full text @ Fish Shellfish Immunol.
Citation
Xu, D., Song, L., Wang, H., Xu, X., Wang, T., Lu, L. (2015) Proteomic analysis of cellular protein expression profiles in response to grass carp reovirus infection. Fish & shellfish immunology. 44(2):515-24.
Abstract
Grass carp (Ctenopharyngodon idella) hemorrhagic disease, caused by grass carp reovirus (GCRV), is emerging as a serious problem in grass carp aquaculture. To better understand the molecular responses to GCRV infection, two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorption/ionization tandem mass spectroscopy were performed to investigate altered proteins in C. idella kidney (CIK) cells. Differentially expressed proteins in mock infected CIK cells and GCRV-infected CIK cells were compared. Twenty-three differentially expressed spots were identified (22 upregulated spots and 1 downregulated spot), which included cytoskeleton proteins, macromolecular biosynthesis-associated proteins, stress response proteins, signal transduction proteins, energy metabolism-associated proteins and ubiquitin proteasome pathway-associated proteins. Moreover, 10 of the corresponding genes of the differentially expressed proteins were quantified by real-time reverse transcription polymerase chain reaction to examine their transcriptional profiles. The T cell internal antigen 1(TIA1) and Ras-GTPase-activating SH3-domain-binding protein1(G3BP1) of the cellular stress granule pathway from grass carp Ctenopharyngodon idella (designated as CiTIA1 and CiG3BP1) were upregulated and downregulated during GCRV infection, respectively. The full-length cDNA of CiTIA1 was 2753 bp, with an open reading frame (ORF) of 1155bp, which encodes a putative 385-amino acid protein. The full-length cDNA of CiG3BP1 comprised a 2271bp ORF of 1455bp that encodes a putative 485-amino acid protein. Phylogenetic analysis revealed that the complete ORFs of CiTIA1 and CiG3BP1 were very similar to zebrafish and well characterized mammalian homologs. The expressions of the cellular proteins CiTIA1 and CiG3BP1 in response to GCRV were validated by western blotting. This study provides useful information on the proteomic and cellular stress granule pathway's responses to GCRV infection, which adds to our understanding of viral pathogenesis.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping