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Optimizing environmental safety and cell-killing potential of oncolytic Newcastle Disease virus with modifications of the V, F and HN genes
被引:4
|作者:
de Graaf, J. Frederique
[1
]
van Nieuwkoop, Stefan
[1
]
Bestebroer, Theo
[1
]
Groeneveld, Daphne
[1
]
van Eijck, Casper H. J.
[2
]
Fouchier, Ron A. M.
[1
]
van den Hoogen, Bernadette G.
[1
]
机构:
[1] Erasmus MC, Virosci Dept, Rotterdam, Netherlands
[2] Erasmus MC, Dept Surg, Rotterdam, Netherlands
来源:
关键词:
FUSION PROTEIN;
CLEAVAGE SITE;
INTERFERON;
PATHOGENICITY;
REPLICATION;
DETERMINANT;
EXPRESSION;
INDUCTION;
VIRULENCE;
ALPHA;
D O I:
10.1371/journal.pone.0263707
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Newcastle Disease Virus (NDV) is an avian RNA virus, which was shown to be effective and safe for use in oncolytic viral therapy for several tumour malignancies. The presence of a multi basic cleavage site (MBCS) in the fusion protein improved its oncolytic efficacy in vitro and in vivo. However, NDV with a MBCS can be virulent in poultry. We aimed to develop an NDV with a MBCS but with reduced virulence for poultry while remaining effective in killing human tumour cells. To this end, the open reading frame of the V protein, an avian specific type I interferon antagonist, was disrupted by introducing multiple mutations. NDV with a mutated V gene was attenuated in avian cells and chicken and duck eggs. Although this virus still killed tumour cells, the efficacy was reduced compared to the virulent NDV. Introduction of various mutations in the fusion (F) and hemagglutinin-neuraminidase (HN) genes slightly improved this efficacy. Taken together, these data demonstrated that NDV with a MBCS but with abrogation of the V protein ORF and mutations in the F and HN genes can be safe for evaluation in oncolytic viral therapy.
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页数:19
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