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Research Note: Duck plague virus glycoprotein I influences cell–cell spread and final envelope acquisition

To determine the role of glycoprotein I (gI) in duck plague virus (DPV), a gI-deleted mutant (BAC-CHv-ΔgI) and a gI-revertant virus (BAC-CHv-ΔgI Rev) were constructed by using a markerless two-step Red recombination system implemented on the DPV genome cloned into a bacterial artificial chromosome (...

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Detalles Bibliográficos
Autores principales: Liu, Tian, Wang, Mingshu, Cheng, Anchun, Jia, Renyong, Wu, Ying, Yang, Qiao, Zhu, Dekang, Chen, Shun, Liu, Mafeng, Zhao, Xinxin, Zhang, Shaqiu, Huang, Juan, Mao, Sai, Ou, Xumin, Gao, Qun, Wen, XingJian, Sun, Di, Liu, Yunya, Yu, Yanling, Zhang, Ling, Tian, Bin, Pan, Leichang, Chen, Xiaoyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7704973/
https://www.ncbi.nlm.nih.gov/pubmed/33248580
http://dx.doi.org/10.1016/j.psj.2020.08.065
Descripción
Sumario:To determine the role of glycoprotein I (gI) in duck plague virus (DPV), a gI-deleted mutant (BAC-CHv-ΔgI) and a gI-revertant virus (BAC-CHv-ΔgI Rev) were constructed by using a markerless two-step Red recombination system implemented on the DPV genome cloned into a bacterial artificial chromosome (BAC). Mutants were characterized on duck embryo fibroblast (DEF) cells compared with wild-type virus. BAC-CHv-ΔgI produced viral plaques on DEF cells that were on average approximately 57.2% smaller than those produced by BAC-CHv-ΔgI Rev and wild-type virus. Electron microscopy confirmed that deleting of gI resulted in nucleocapsids accumulated around the cytoplasm vesicles and few of them could complete the final envelopment process. These results clearly indicated that DPV gI plays significant roles in viral cell-cell spread and viral final envelopment process.