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A Fosmid-Based System for the Generation of Recombinant Cercopithecine Alphaherpesvirus 2 Encoding Reporter Genes

机译:基于Fosmid的系统生成重组Cercopithecine Alphaherpesvirus 2编码报告基因。

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摘要

The transmission of Macacine alphaherpesvirus 1 (McHV-1) from macaques, the natural host, to humans causes encephalitis. In contrast, human infection with Cercopithecine alphaherpesvirus 2 (CeHV-2), a closely related alphaherpesvirus from African vervet monkeys and baboons, has not been reported and it is believed that CeHV-2 is apathogenic in humans. The reasons for the differential neurovirulence of McHV-1 and CeHV-2 have not been explored on a molecular level, in part due to the absence of systems for the production of recombinant viruses. Here, we report the generation of a fosmid-based system for rescue of recombinant CeHV-2. Moreover, we show that, in this system, recombineering can be used to equip CeHV-2 with reporter genes. The recombinant CeHV-2 viruses replicated with the same efficiency as uncloned, wt virus and allowed the identification of cell lines that are highly susceptible to CeHV-2 infection. Collectively, we report a system that allows rescue and genetic modification of CeHV-2 and likely other alphaherpesviruses. This system should aid future analysis of CeHV-2 biology.
机译:Macacine alphaherpesvirus 1(McHV-1)从猕猴(天然宿主)向人类的传播会导致脑炎。相反,尚未报道人类感染了非洲非洲黑长尾猴和狒狒的密切相关的丙型上皮氨酸α疱疹病毒2(CeHV-2),并且认为CeHV-2对人类无致病性。尚未在分子水平上探讨McHV-1和CeHV-2差异神经毒力的原因,部分原因是缺乏生产重组病毒的系统。在这里,我们报告了基于化石的系统的生成,用于挽救重组CeHV-2。此外,我们表明,在该系统中,重组可用于为CeHV-2配备报道基因。重组CeHV-2病毒的复制效率与未克隆的wt病毒相同,可鉴定高度易受CeHV-2感染的细胞系。总体而言,我们报告了一个系统,该系统可以对CeHV-2和其他可能的α疱疹病毒进行抢救和基因修饰。该系统应有助于CeHV-2生物学的未来分析。

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