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African swine fever virus (ASFV) protection mediated by NH/P68 and NH/P68 recombinant live-attenuated viruses

机译:非洲猪瘟病毒(ASFV)保护由NH / P68和NH / P68重组活减毒病毒介导

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摘要

The risk of spread of African swine fever virus (ASFV) from Russia and Caucasian areas to several EU countries has recently emerged, making it imperative to improve our knowledge and defensive tools against this important pathogen. The ASFV genome encodes many genes which are not essential for virus replication but are known to control host immune evasion, such as NFxB and the NFAT regulator A238L, the apoptosis inhibitor A224L, the MHC-I antigen presenting modulator EP153R, and the A276R gene, involved in modulating type I IFN. These genes are hypothesized to be involved in virulence of the genotype I parental ASFV NH/P68. We here describe the generation of putative live attenuated vaccines (LAV) prototypes by constructing recombinant NH/P68 viruses lacking these specific genes and containing specific markers. (C) 2018 Elsevier Ltd. All rights reserved.
机译:最近出现了来自俄罗斯和高加索地区的非洲猪瘟病毒(ASFV)的风险,最近出现了几个欧盟国家,使我们对抗这一重要病原体的知识和防御工具必须迫切。 ASFV基因组编码许多基因对病毒复制不是必不可少的基因,但是已知控制宿主免疫逃逸,例如NFXB和NFAT调节剂A238L,凋亡抑制剂A224L,MHC-I抗原呈现调节剂EP153R和A276R基因, 参与调制I IFN类型。 这些基因被假设涉及基因型I父母ASFV NH / P68的毒力。 我们在这里描述了通过构建缺乏这些特定基因和含有特异性标记的重组NH / P68病毒来描述推定的现场减毒疫苗(LAV)原型。 (c)2018年elestvier有限公司保留所有权利。

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