Identification and characterization of duck plague virus glycoprotein C gene and gene product

被引:27
作者
Lian, Bei [1 ]
Xu, Chao [1 ]
Cheng, Anchun [1 ,2 ,3 ]
Wang, Mingshu [1 ,2 ]
Zhu, Dekang [1 ,2 ]
Luo, Qihui [2 ]
Jia, Renyong [2 ]
Bi, Fengjun [2 ]
Chen, Zhengli [2 ]
Zhou, Yi [2 ]
Yang, Zexia [2 ]
Chen, Xiaoyue [1 ,2 ,3 ]
机构
[1] Sichuan Agr Univ, Avian Dis Res Ctr, Coll Vet Med, Yaan 625014, Sichuan, Peoples R China
[2] Key Lab Anim Dis & Human Hlth Sichuan Prov, Yaan 625014, Sichuan, Peoples R China
[3] Sichuan Agr Univ, Epizoot Dis Inst, Yaan 625014, Sichuan, Peoples R China
关键词
HERPES-SIMPLEX-VIRUS; SYNONYMOUS CODON USAGE; CYTOTOXIC T-LYMPHOCYTES; PSEUDORABIES VIRUS; ENTERITIS VIRUS; HEPARAN-SULFATE; BINDING DOMAIN; POLYCLONAL ANTIBODY; IMMUNE EVASION; IN-VIVO;
D O I
10.1186/1743-422X-7-349
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Viral envelope proteins have been proposed to play significant roles in the process of viral infection. Results: In this study, an envelope protein gene, gC (NCBI GenBank accession no. EU076811), was expressed and characterized from duck plague virus (DPV), a member of the family herpesviridae. The gene encodes a protein of 432 amino acids with a predicted molecular mass of 45 kDa. Sequence comparisons, multiple alignments and phylogenetic analysis showed that DPV gC has several features common to other identified herpesvirus gC, and was genetically close to the gallid herpervirus. Antibodies raised in rabbits against the pET32a-gC recombinant protein expressed in Escherichia coli BL21 (DE3) recognized a 45-KDa DPV-specific protein from infected duck embryo fibroblast (DEF) cells. Transcriptional and expression analysis, using real-time fluorescent quantitative PCR (FQ-PCR) and Western blot detection, revealed that the transcripts encoding DPV gC and the protein itself appeared late during infection of DEF cells. Immunofluorescence localization further demonstrated that the gC protein exhibited substantial cytoplasm fluorescence in DPV-infected DEF cells. Conclusions: In this work, the DPV gC protein was successfully expressed in a prokaryotic expression system, and we presented the basic properties of the DPV gC product for the first time. These properties of the gC protein provided a prerequisite for further functional analysis of this gene.
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页数:11
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