首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Construction of an attenuated Tian Tan vaccinia virus strain by deletion of TA35R and TJ2R genes
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Construction of an attenuated Tian Tan vaccinia virus strain by deletion of TA35R and TJ2R genes

机译:通过缺失Ta35R和TJ2R基因抑制天褐色痘病毒株的构建

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rVTT-TA35-TJ, an attenuated vaccinia virus Tian Tan strain (VTT), was constructed by knocking out two non-essential gene fragments (TA35R and TJ2R) related to virulence, immunomodulation, and host range; and by combining double marker screening with exogenous and endogenous selectable marker knock-out techniques. Here, the shuttle plasmids pSK-TA35 and pSK-TJ were constructed, containing two pairs of recombinant arms: early and late strong promoter pE/L and EGFP as an exogenous selectable marker. The recombinant vaccinia virus rVTT-TA35-TJ without exogenous selection markers was then obtained through homologous recombination technology and the Cre/loxP system. Knocking out the two gene fragments does not affect the replication ability of the virus and displays a good genetic stability. Furthermore, a series ofin vivoandin vitroexperiments demonstrate that although virulence of rVTT-TA35-TJ is attenuated significantly, high immunogenicity was maintained. These results support the potential development of rVTT-TA35-TJ as a safe viral vector or vaccine.
机译:RVTT-TA35-TJ是一种减毒的痘苗病毒田TAN TAN TAN TAN TAN菌株(VTT),通过敲出与毒力,免疫调节和主机范围有关的两个非必需基因片段(TA35R和TJ2R)构建;通过将双重标记筛选与外源性和内源性选择标记敲除技术相结合。在此,构建了梭子质粒psk-ta35和psk-tj,含有两对重组臂:早期和晚期强启动子PE / L和EGFP作为外源选择标记。然后通过同源重组技术和CRE / LOXP系统获得没有外源选择标记的重组痘苗病毒RVTT-TA35-Tj。敲除两种基因片段不影响病毒的复制能力,并显示出良好的遗传稳定性。此外,一系列vivoandin vitropperiments表明,尽管Rvtt-ta35-tj的毒力显着衰减,但保持高免疫原性。这些结果支持RVTT-TA35-TJ的潜在发展,作为安全的病毒载体或疫苗。

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