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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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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. |
format | Online Article Text |
id | pubmed-3120784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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