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Characterization of duck enteritis virus UL53 gene and glycoprotein K

BACKGROUND: Most of the previous research work had focused on the epidemiology and prevention of duck enteritis virus (DEV). Whilst with the development of protocols in molecular biology, nowadays more and more information about the genes of DEV was reported. But little information about DEV UL53 ge...

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Autores principales: Zhang, Shunchuan, Xiang, Jun, Cheng, Anchun, Wang, Mingshu, Wu, Ying, Yang, Xiaoyuan, Zhu, Dekang, Jia, Renyong, Luo, Qihui, Chen, Zhengli, Chen, Xiaoyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120784/
https://www.ncbi.nlm.nih.gov/pubmed/21586146
http://dx.doi.org/10.1186/1743-422X-8-235
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author Zhang, Shunchuan
Xiang, Jun
Cheng, Anchun
Wang, Mingshu
Wu, Ying
Yang, Xiaoyuan
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Chen, Zhengli
Chen, Xiaoyue
author_facet Zhang, Shunchuan
Xiang, Jun
Cheng, Anchun
Wang, Mingshu
Wu, Ying
Yang, Xiaoyuan
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Chen, Zhengli
Chen, Xiaoyue
author_sort Zhang, Shunchuan
collection PubMed
description BACKGROUND: Most of the previous research work had focused on the epidemiology and prevention of duck enteritis virus (DEV). Whilst with the development of protocols in molecular biology, nowadays more and more information about the genes of DEV was reported. But little information about DEV UL53 gene and glycoprotein K(gK) was known except our reported data. RESULTS: In our paper, the fluorescent quantitative real-time PCR(FQ-RT-PCR) assay and nucleic acid inhibition test were used to study the transcription characteristic of the DEV UL53 gene. Except detecting the mRNA of DEV UL53 gene, the product gK encoded by UL53 gene was detected through the expression kinetics of UL53 gene by the purified rabbit anti-UL53 protein polyclonal antibodies. Western-blotting and indirect immunofluorescence assays were used to detect gK. From the results of these experiments, the UL53 gene and gK were respectively identified as a late gene and a really late protein. On the other hand, the indirect immunofluorescence assay provided another information that the intracellular localization of DEV gK was mainly distributed in cytoplasm. CONCLUSIONS: By way of conclusions, we conceded that DEV UL53 gene is a really late gene, which is coincident with properties of UL53 homologs from other herpesvirus, such as ILTV(Infectious Laryngotracheitis virus) and HSV-1(Herpes simplex virus type 1). The properties of intracellular localization about gK protein provided a foundation for further functional analysis and further studies will be focused on constructing of the UL53 gene DEV mutant.
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spelling pubmed-31207842011-06-23 Characterization of duck enteritis virus UL53 gene and glycoprotein K Zhang, Shunchuan Xiang, Jun Cheng, Anchun Wang, Mingshu Wu, Ying Yang, Xiaoyuan Zhu, Dekang Jia, Renyong Luo, Qihui Chen, Zhengli Chen, Xiaoyue Virol J Research BACKGROUND: Most of the previous research work had focused on the epidemiology and prevention of duck enteritis virus (DEV). Whilst with the development of protocols in molecular biology, nowadays more and more information about the genes of DEV was reported. But little information about DEV UL53 gene and glycoprotein K(gK) was known except our reported data. RESULTS: In our paper, the fluorescent quantitative real-time PCR(FQ-RT-PCR) assay and nucleic acid inhibition test were used to study the transcription characteristic of the DEV UL53 gene. Except detecting the mRNA of DEV UL53 gene, the product gK encoded by UL53 gene was detected through the expression kinetics of UL53 gene by the purified rabbit anti-UL53 protein polyclonal antibodies. Western-blotting and indirect immunofluorescence assays were used to detect gK. From the results of these experiments, the UL53 gene and gK were respectively identified as a late gene and a really late protein. On the other hand, the indirect immunofluorescence assay provided another information that the intracellular localization of DEV gK was mainly distributed in cytoplasm. CONCLUSIONS: By way of conclusions, we conceded that DEV UL53 gene is a really late gene, which is coincident with properties of UL53 homologs from other herpesvirus, such as ILTV(Infectious Laryngotracheitis virus) and HSV-1(Herpes simplex virus type 1). The properties of intracellular localization about gK protein provided a foundation for further functional analysis and further studies will be focused on constructing of the UL53 gene DEV mutant. BioMed Central 2011-05-17 /pmc/articles/PMC3120784/ /pubmed/21586146 http://dx.doi.org/10.1186/1743-422X-8-235 Text en Copyright ©2011 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhang, Shunchuan
Xiang, Jun
Cheng, Anchun
Wang, Mingshu
Wu, Ying
Yang, Xiaoyuan
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Chen, Zhengli
Chen, Xiaoyue
Characterization of duck enteritis virus UL53 gene and glycoprotein K
title Characterization of duck enteritis virus UL53 gene and glycoprotein K
title_full Characterization of duck enteritis virus UL53 gene and glycoprotein K
title_fullStr Characterization of duck enteritis virus UL53 gene and glycoprotein K
title_full_unstemmed Characterization of duck enteritis virus UL53 gene and glycoprotein K
title_short Characterization of duck enteritis virus UL53 gene and glycoprotein K
title_sort characterization of duck enteritis virus ul53 gene and glycoprotein k
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120784/
https://www.ncbi.nlm.nih.gov/pubmed/21586146
http://dx.doi.org/10.1186/1743-422X-8-235
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