Mei Ya-Fang, Wu Haidong, Hultenby Kjell, Silver Jim
Department of Clinical Microbiology and Virology, Umeå University, SE-901 85 Umeå, Sweden.
Division of Clinical Research Centre, Department of Laboratory Medicine, Karolinska Institute, SE-14186 Stockholm, Sweden.
Virology. 2016 Oct;497:198-210. doi: 10.1016/j.virol.2016.07.026. Epub 2016 Aug 3.
Conventional adenovirus vectors harboring E1 or E3 deletions followed by the insertion of an exogenous gene show considerably reduced virion stability. Here, we report strategies to generate complete replication-competent Ad11p(RCAd11p) vectors that overcome the above disadvantage. A GFP cassette was successfully introduced either upstream of E1A or in the E3A region. The resulting vectors showed high expression levels of the hexon and E1genes and also strongly induced the cytopathic effect in targeted cells. When harboring oversized genomes, the RCAd11pE1 and RCAd11pE3 vectors showed significantly improved heat stability in comparison to Ad11pwt;of the three, RCAd11pE3 was the most tolerant to heat treatment. Electron microscopy showed that RCAd11pE3, RCAd11pE1, Ad11pwt, and Ad11pE1 Delmanifested dominant, moderate, minimum, or no full virus particles after heat treatment at 47°C for 5h. Our results demonstrated that both genome size and the insertion site in the viral genome affect virion stability.
携带E1或E3缺失并随后插入外源基因的传统腺病毒载体显示出病毒体稳定性显著降低。在此,我们报告了生成完全具有复制能力的Ad11p(RCAd11p)载体的策略,该策略克服了上述缺点。绿色荧光蛋白(GFP)盒成功地被引入到E1A上游或E3A区域。所得载体显示出六邻体和E1基因的高表达水平,并且还在靶细胞中强烈诱导细胞病变效应。当携带超大基因组时,与野生型Ad11p相比,RCAd11pE1和RCAd11pE3载体显示出显著提高的热稳定性;在这三者中,RCAd11pE3对热处理的耐受性最强。电子显微镜显示,在47°C热处理5小时后,RCAd11pE3、RCAd11pE1、Ad11pwt和Ad11pE1 Del分别表现出占主导、中等、最小或无完整病毒颗粒。我们的结果表明,基因组大小和病毒基因组中的插入位点都会影响病毒体稳定性。