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

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 herpesv...

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Autores principales: Lian, Bei, Xu, Chao, Cheng, Anchun, Wang, Mingshu, Zhu, Dekang, Luo, Qihui, Jia, Renyong, Bi , Fengjun, Chen, Zhengli, Zhou, Yi, Yang, Zexia, Chen, Xiaoyue
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004831/
https://www.ncbi.nlm.nih.gov/pubmed/21110887
http://dx.doi.org/10.1186/1743-422X-7-349
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author Lian, Bei
Xu, Chao
Cheng, Anchun
Wang, Mingshu
Zhu, Dekang
Luo, Qihui
Jia, Renyong
Bi , Fengjun
Chen, Zhengli
Zhou, Yi
Yang, Zexia
Chen, Xiaoyue
author_facet Lian, Bei
Xu, Chao
Cheng, Anchun
Wang, Mingshu
Zhu, Dekang
Luo, Qihui
Jia, Renyong
Bi , Fengjun
Chen, Zhengli
Zhou, Yi
Yang, Zexia
Chen, Xiaoyue
author_sort Lian, Bei
collection PubMed
description 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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spelling pubmed-30048312010-12-21 Identification and characterization of duck plague virus glycoprotein C gene and gene product Lian, Bei Xu, Chao Cheng, Anchun Wang, Mingshu Zhu, Dekang Luo, Qihui Jia, Renyong Bi , Fengjun Chen, Zhengli Zhou, Yi Yang, Zexia Chen, Xiaoyue Virol J Research 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. BioMed Central 2010-11-27 /pmc/articles/PMC3004831/ /pubmed/21110887 http://dx.doi.org/10.1186/1743-422X-7-349 Text en Copyright ©2010 Lian et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lian, Bei
Xu, Chao
Cheng, Anchun
Wang, Mingshu
Zhu, Dekang
Luo, Qihui
Jia, Renyong
Bi , Fengjun
Chen, Zhengli
Zhou, Yi
Yang, Zexia
Chen, Xiaoyue
Identification and characterization of duck plague virus glycoprotein C gene and gene product
title Identification and characterization of duck plague virus glycoprotein C gene and gene product
title_full Identification and characterization of duck plague virus glycoprotein C gene and gene product
title_fullStr Identification and characterization of duck plague virus glycoprotein C gene and gene product
title_full_unstemmed Identification and characterization of duck plague virus glycoprotein C gene and gene product
title_short Identification and characterization of duck plague virus glycoprotein C gene and gene product
title_sort identification and characterization of duck plague virus glycoprotein c gene and gene product
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004831/
https://www.ncbi.nlm.nih.gov/pubmed/21110887
http://dx.doi.org/10.1186/1743-422X-7-349
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