| Literature DB >> 35751792 |
Jie Ni1,2,3, Qing Chen1,2,3, Tianxing Liao1,2,3, Jing Deng1,4,2,3, Yu Chen1,2,3, Jiao Hu1,2,3, Shunlin Hu1,2,3, Zenglei Hu5,6,7,8, Xiufan Liu9,10,11,12.
Abstract
Newcastle disease virus (NDV) is an important pathogen for poultry and is used as a vector for developing novel poultry vaccines. Previous studies showed that foreign gene insertion in NDV vector decreases virulence determined by in vitro assays; however, the impact of foreign gene expression on the pathogenicity of NDV in susceptible chickens is not fully investigated. In this study, a recombinant NDV based on a velogenic strain carrying the orange fluorescent protein (OFP) gene between the phosphoprotein (P) and matrix (M) genes was generated using reverse genetics. Biological characteristics, including virus replication, virulence, and OFP expression, and the pathogenicity in chickens were evaluated. The recombinant NDV showed comparable replication capacity in eggs and cells as the parental virus, whereas OFP insertion resulted in a mild impairment of virulence, evidenced by longer mean death time in embryos. High OFP expression was detected in the cells inoculated with the recombinant NDV. In addition, the recombinant NDV induced delayed onset of disease, lower severity of clinical signs, and lower mortality in chickens compared to the parental virus. Moreover, high titers of the parental virus were detected in the spleen, lung, and intestinal tract, while no recombinant NDV was recovered from these tissues. Our findings suggest that in vitro characteristics related to the insertion of the OFP gene in a virulent NDV do not correlate to alteration of the pathogenicity in chickens. Our results provided new information regarding assessment of the impact of foreign gene expression on the pathogenicity of NDV.Entities:
Keywords: Foreign gene expression; Newcastle disease virus; Orange fluorescent protein; Pathogenicity; Reverse genetics; Virus vector
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Year: 2022 PMID: 35751792 DOI: 10.1007/s11262-022-01922-8
Source DB: PubMed Journal: Virus Genes ISSN: 0920-8569 Impact factor: 2.198