Author:
Shen Bingjie,Li Yunjiao,Cheng Anchun,Wang Mingshu,Wu Ying,Yang Qiao,Jia Renyong,Tian Bin,Ou Xumin,Mao Sai,Sun Di,Zhang Shaqiu,Zhu Dekang,Chen Shun,Liu Mafeng,Zhao Xin-Xin,Huang Juan,Gao Qun,Liu Yunya,Yu Yanling,Zhang Ling,Pan Leichang
Abstract
Duck plague virus (DPV) can cause high morbidity and mortality in many waterfowl species within the order Anseriformes. The DPV genome contains 78 open reading frames (ORFs), among which the LORF2, LORF3, LORF4, LORF5, and SORF3 genes are unique genes of avian herpesvirus. In this study, to investigate the role of this unique LORF5 gene in DPV proliferation, we generated a recombinant virus that lacks the LORF5 gene by a two-step red recombination system, which cloned the DPV Chinese virulent strain (DPV CHv) genome into a bacterial artificial chromosome (DPV CHv-BAC); the proliferation law of LORF5-deleted mutant virus on DEF cells and the effect of LORF5 gene on the life cycle stages of DPV compared with the parent strain were tested. Our data revealed that the LORF5 gene contributes to the cell-to-cell transmission of DPV but is not relevant to virus invasion, replication, assembly, and release formation. Taken together, this study sheds light on the role of the avian herpesvirus-specific gene LORF5 in the DPV proliferation life cycle. These findings lay the foundation for in-depth functional studies of the LORF5 gene in DPV or other avian herpesviruses.
Subject
Microbiology (medical),Microbiology
Cited by
7 articles.
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