Development of a recombinant non-replicating Newcastle disease virus

被引:0
|
作者
Cheow, Pheik-Sheen [1 ]
Tan, Tiong Kit [2 ]
Song, Adelene Ai-Lian [3 ]
Yusoff, Khatijah [1 ]
Chia, Suet Lin [1 ,3 ,4 ]
机构
[1] Malaysia Genome & Vaccine Inst, Kajang 43000, Selangor, Malaysia
[2] Univ Oxford, MRC Weatherall Inst Mol Med, MRC Translate Immune Discovery Unit, Oxford, England
[3] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Microbiol, Serdang, Malaysia
[4] Univ Putra Malaysia, Inst Biosci, UPM MAKNA Canc Res Lab, Serdang, Malaysia
关键词
Newcastle disease virus; avian virus; truncated anti-genome; reverse genetic system; viral vector; non-replicating; ONCOLYTIC VIRUS; REPLICATION; SEQUENCES; THERAPY; VACCINE; TRIAL;
D O I
10.1080/03079457.2024.2403412
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Newcastle disease virus (NDV) is an avian orthoavulavirus I that causes high morbidity and mortality in birds, depending on the pathotype of the virus. Several clinical studies have shown that NDV is a promising oncolytic virus for cancer therapies, yet its application to clinics is restricted due to the pathogenicity of this virus in poultry. Hence, it is important to produce a recombinant NDV (rNDV) with reduced virulence to make it a fit candidate as an oncolytic virus. In this study, we aimed to produce a rNDV with a truncated ant-igenome via reverse genetics to render it non-replicating (nr). The genes responsible for replication were removed from the NDV genome. The rescued nr-NDV was verified, propagated, and purified from tissue culture medium. The virus failed to propagate in embryonated eggs, confirming its non-replicating property. The virus retained its oncolytic activities similar to that of the replicating rAF-GFP as observed in a cell viability assay when a breast cancer cell line, MCF-7, was treated with the virus. In conclusion, this study has successfully generated a system to produce a non-replicating NDV which can be used as a viral vector for heterologous protein delivery, as a safer alternative compared to the virulent strains as an oncolytic virus.RESEARCH HIGHLIGHTSDevelopment of nr-NDV.Reverse transfection was applied for the recovery of nr-NDV.Propagation of nr-NDV was done by sub-passaging transfected BSR T7/5 cells.Safety profile was done to prove that the nr-NDV is non-replicating.
引用
收藏
页码:149 / 157
页数:9
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