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Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread

Duck plague virus (DPV) is one of the major infectious and fatal diseases of geese, ducks, and other wild waterfowl. The DPV UL49 gene product VP22 is one of the most abundant tegument proteins. However, the role of the DPV VP22 is enigmatic to be clarified. In this study, we found deletion of the U...

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Autores principales: Wu, Liping, Wang, Mingshu, Cheng, Anchun, Tian, Bin, Huang, Juan, Wu, Ying, Yang, Qiao, Ou, Xumin, Sun, Di, Zhang, Shaqiu, Zhao, Xinxin, Gao, Qun, He, Yu, Zhu, Dekang, Chen, Shun, Liu, Mafeng, Jia, Renyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351120/
https://www.ncbi.nlm.nih.gov/pubmed/37461115
http://dx.doi.org/10.1186/s13567-023-01191-9
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author Wu, Liping
Wang, Mingshu
Cheng, Anchun
Tian, Bin
Huang, Juan
Wu, Ying
Yang, Qiao
Ou, Xumin
Sun, Di
Zhang, Shaqiu
Zhao, Xinxin
Gao, Qun
He, Yu
Zhu, Dekang
Chen, Shun
Liu, Mafeng
Jia, Renyong
author_facet Wu, Liping
Wang, Mingshu
Cheng, Anchun
Tian, Bin
Huang, Juan
Wu, Ying
Yang, Qiao
Ou, Xumin
Sun, Di
Zhang, Shaqiu
Zhao, Xinxin
Gao, Qun
He, Yu
Zhu, Dekang
Chen, Shun
Liu, Mafeng
Jia, Renyong
author_sort Wu, Liping
collection PubMed
description Duck plague virus (DPV) is one of the major infectious and fatal diseases of geese, ducks, and other wild waterfowl. The DPV UL49 gene product VP22 is one of the most abundant tegument proteins. However, the role of the DPV VP22 is enigmatic to be clarified. In this study, we found deletion of the UL49 gene resulted in reduced viral growth curve and smaller plaque size in duck embryo fibroblast (DEF) cells, confirming that DPV VP22 is required for efficient viral growth in vitro. In addition, deletion of the UL49 gene inhibited the secondary envelopment of the virus, the release of viral particles, and the spread of viruses between cells. Our study signified the importance of VP22 for DPV secondary envelopment, release, cell-to-cell spread, and accumulation of viral RNA. These findings provide a basis for further study of the function of VP22 in DPV or other herpesviruses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-023-01191-9.
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spelling pubmed-103511202023-07-18 Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread Wu, Liping Wang, Mingshu Cheng, Anchun Tian, Bin Huang, Juan Wu, Ying Yang, Qiao Ou, Xumin Sun, Di Zhang, Shaqiu Zhao, Xinxin Gao, Qun He, Yu Zhu, Dekang Chen, Shun Liu, Mafeng Jia, Renyong Vet Res Research Article Duck plague virus (DPV) is one of the major infectious and fatal diseases of geese, ducks, and other wild waterfowl. The DPV UL49 gene product VP22 is one of the most abundant tegument proteins. However, the role of the DPV VP22 is enigmatic to be clarified. In this study, we found deletion of the UL49 gene resulted in reduced viral growth curve and smaller plaque size in duck embryo fibroblast (DEF) cells, confirming that DPV VP22 is required for efficient viral growth in vitro. In addition, deletion of the UL49 gene inhibited the secondary envelopment of the virus, the release of viral particles, and the spread of viruses between cells. Our study signified the importance of VP22 for DPV secondary envelopment, release, cell-to-cell spread, and accumulation of viral RNA. These findings provide a basis for further study of the function of VP22 in DPV or other herpesviruses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-023-01191-9. BioMed Central 2023-07-17 2023 /pmc/articles/PMC10351120/ /pubmed/37461115 http://dx.doi.org/10.1186/s13567-023-01191-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wu, Liping
Wang, Mingshu
Cheng, Anchun
Tian, Bin
Huang, Juan
Wu, Ying
Yang, Qiao
Ou, Xumin
Sun, Di
Zhang, Shaqiu
Zhao, Xinxin
Gao, Qun
He, Yu
Zhu, Dekang
Chen, Shun
Liu, Mafeng
Jia, Renyong
Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
title Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
title_full Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
title_fullStr Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
title_full_unstemmed Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
title_short Duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
title_sort duck plague virus tegument protein vp22 plays a key role in the secondary envelopment and cell-to-cell spread
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351120/
https://www.ncbi.nlm.nih.gov/pubmed/37461115
http://dx.doi.org/10.1186/s13567-023-01191-9
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