首页> 外文期刊>Virus Genes >Functional analysis of Spodoptera litura nucleopolyhedrovirus p49 gene during Autographa californica nucleopolyhedrovirus infection of SpLi-221 cells.
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Functional analysis of Spodoptera litura nucleopolyhedrovirus p49 gene during Autographa californica nucleopolyhedrovirus infection of SpLi-221 cells.

机译:斜纹夜蛾核多角体病毒p49基因在加利福尼亚州Autographa californica核多角体病毒感染SpLi-221细胞期间的功能分析。

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摘要

The Spodoptera litura nucleopolyhedrovirus (SpltNPV) antiapoptotic gene Splt-p49 is able to rescue replication of a p35-null Autographa californica nucleopolyhedrovirus (AcMNPV) in AcMNPV-permissive Sf9 cells. In this study, an AcMNPV p35 knockout bacmid was generated through ET homologous recombination in Escherichia coli and designated as vAc(P35-KO). The Splt-p49 gene was transposed into the polyhedrin locus of vAc(P35-KO) to investigate if Splt-p49 has any antiapoptotic activity in the context of AcMNPV infection of AcMNPV-nonpermissive SpLi-221 cells. Our results demonstrated that Splt-p49 could not inhibit the apoptosis induced by AcMNPV infection of SpLi-221 cells when it was under the control of its native promoter. Western blot analysis showed that Splt-P49 was poorly expressed. When the expression of Splt-P49 was under the control of Drosophila hsp70 promoter, the expression of Splt-P49 was advanced, and a higher level of Splt-P49 was detected. As a result, the apoptosis of SpLi-221 cells was inhibited; however, budded-virus production did not improve in comparison with that in AcMNPV-infected SpLi-221 cells. These data indicated that there are other barrier(s) to AcMNPV replication in the nonpermissive SpLi-221 cells besides apoptosis.
机译:斜纹夜蛾核多角体病毒(SpltNPV)抗凋亡基因Splt-p49能够挽救pMN无效的加州产的加州产自传粉原核多角体病毒(AcMNPV)在AcMNPV允许的Sf9细胞中的复制。在这项研究中,通过在大肠杆菌中进行ET同源重组产生了AcMNPV p35基因敲除杆粒,并将其命名为vAc(P35-KO)。将Splt-p49基因转座到vAc(P35-KO)的多面体基因座中,以研究在AcMNPV不允许的SpMN-221细胞被AcMNPV感染的情况下Splt-p49是否具有抗凋亡活性。我们的结果表明,当Splt-p49受其天然启动子控制时,它不能抑制AcMNPV感染SpLi-221细胞诱导的凋亡。蛋白质印迹分析表明Splt-P49表达差。当Splt-P49的表达受果蝇hsp70启动子的控制时,Splt-P49的表达增加,并且检测到较高水平的Splt-P49。结果,SpLi-221细胞的凋亡被抑制。但是,与AcMNPV感染的SpLi-221细胞相比,芽病毒的生产没有改善。这些数据表明在非许可的SpLi-221细胞中除了凋亡外,还存在其他阻碍AcMNPV复制的障碍。

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