首页> 外文期刊>Veterinary Research: A Journal on Animal Infection >Construction and testing of a novel host-range defective myxoma virus vaccine with the M063 gene inactivated that is non-permissive for replication in rabbit cells.
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Construction and testing of a novel host-range defective myxoma virus vaccine with the M063 gene inactivated that is non-permissive for replication in rabbit cells.

机译:M063基因失活的新型宿主范围缺陷粘液瘤病毒疫苗的构建和测试,该疫苗不允许在兔细胞中复制。

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摘要

Deletion of the M063 gene from myxoma virus produces a virus that is unable to replicate in rabbit cells in vitro or in live rabbits but can be propagated in non-rabbit cell lines. A targeted M063 deletion mutant was constructed in the attenuated Uriarra strain of myxoma virus and the ability of this virus to act as a safe, non-transmissible vaccine against myxomatosis was tested in outbred laboratory rabbits. Immunization with the M063 deletion vaccine provided good short-term protection against lethal challenge with virulent myxoma virus. Long-term protection was similar to reported results with heterologous live virus, with some rabbits protected but others succumbing to challenge. Replication-deficient poxvirus vaccines, like the Modified Vaccinia Virus Ankara (MVA) in man and the myxoma virus vaccine described here in rabbits, are very attractive from a safety perspective. Seasonal boosting would be predicted to provide long-term protection. Targeted host-range gene deletions could have potential for rapid development of poxvirus vaccines in general.
机译:从粘液瘤病毒中删除M063基因会产生一种病毒,该病毒在体外或活兔中无法在兔细胞中复制,但可以在非兔细胞系中繁殖。在减毒的粘瘤病毒的Uriarra毒株中构建了靶向的M063缺失突变体,并在近交实验室的兔子中测试了该病毒作为安全的,不可传播的抗粘瘤病疫苗的能力。 M063缺失疫苗的免疫为抵抗强毒性粘液瘤病毒的致命攻击提供了良好的短期保护。长期保护与报道的使用异源活病毒的结果相似,有些兔子受到了保护,但另一些却屈服于挑战。从安全角度来看,复制缺陷型痘病毒疫苗,例如人用改良痘苗病毒安卡拉(MVA)和此处描述的兔用粘液瘤病毒疫苗,非常具有吸引力。预计季节性的提振将提供长期保护。一般而言,靶向宿主范围基因的缺失可能具有快速开发痘病毒疫苗的潜力。

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