毒力
新城疫
生物
病毒学
病毒
胚胎化的
微生物学
单反病毒
溶瘤病毒
感染剂量
病毒释放
副粘病毒科
融合蛋白
基因
病毒性疾病
遗传学
重组DNA
作者
Jean de Graaf,Stefan van Nieuwkoop,Dennis de Meulder,Pascal Lexmond,Thijs Kuiken,Dennis Groeneveld,Ron A. M. Fouchier,Bernadette G. van den Hoogen
标识
DOI:10.1016/j.vetmic.2022.109437
摘要
Newcastle Disease virus (NDV) has shown promise as an oncolytic virus for treatment of a wide range of tumours. NDV with a multi-basic cleavage site (MBCS) in the fusion (F) protein (NDV F3aa) has increased oncolytic efficacy in several tumour models, but also increased virulence in chickens compared to non-virulent NDV F0, raising potential environmental safety issues. Previously, we generated a variant of NDV F3aa with a disrupted V protein gene and a substitution of phenylalanine to serine at position 117 of the F protein (NDV F3aa-S-STOPV). Compared to NDV F3aa this virus had decreased virulence in embryonated chicken eggs. In this study, the virulence of the virus was evaluated upon inoculation of six-week-old chickens through a natural infection route and by determination of the intracerebral pathogenicity index (ICPI). Based on these data NDV F3aa-S-STOPV classified as a non-virulent virus. Although NDV F3aa was classified as a virulent virus based on the ICPI, the virus was also less pathogenic than NDV F0 upon inoculation of six-week-old chickens. These data indicate that NDV with a MBCS is not necessarily pathogenic in chickens. In addition, these data show that F3aa-S-STOPV is safe to use in viro-immunotherapies without posing a threat for chickens upon accidental exposure.
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