Molecular, Cellular, and Developmental Biology Program, Division of Biology, 116 Ackert Hall, Kansas State University, Manhattan, KS 66506, USA.
Virology. 2013 Jan 20;435(2):442-52. doi: 10.1016/j.virol.2012.10.015. Epub 2012 Nov 11.
Autographa californica M nucleopolyhedrovirus (AcMNPV) open reading frame 109 (ac109) is conserved in all known baculovirus genomes, suggesting a crucial role in virus replication. Although viruses lacking ac109 have been previously characterized, the phenotypes differ from production of non-infectious virions to lack of virion production. To re-examine ac109 function, we constructed a recombinant AcMNPV bacmid, AcBAC109KO, with a deletion in ac109. We did not detect infectious budded virus after transfection of AcBAC109KO DNA into cells. In the nucleus, nucleocapsids had envelopment defects and polyhedra lacked virions. DNA synthesis and gene expression between AcBAC109KO and a control virus were similar. However, lower levels of non-infectious budded virus were detected from AcBAC109KO DNA-transfected cells compared to the parental virus using Q-PCR to detect viral DNA or by immunoblotting to detect a budded virus protein. Therefore, deletion of ac109 affects envelopment of nucleocapsids in the nucleus and the production of infectious budded virus.
苜蓿银纹夜蛾多核型多角体病毒(AcMNPV)开放阅读框 109(ac109)在所有已知杆状病毒基因组中都保守存在,这表明其在病毒复制中具有关键作用。尽管以前已经对缺乏 ac109 的病毒进行了表征,但表型差异从产生无感染性病毒粒子到缺乏病毒粒子产生不等。为了重新研究 ac109 的功能,我们构建了一个重组 AcMNPV 杆状病毒 bacmid,命名为 AcBAC109KO,该 bacmid 在 ac109 中缺失。我们在将 AcBAC109KO DNA 转染细胞后没有检测到感染性芽生病毒。在细胞核中,核衣壳包被缺陷,多角体缺乏病毒粒子。AcBAC109KO 和对照病毒之间的 DNA 合成和基因表达相似。然而,与亲本病毒相比,从 AcBAC109KO DNA 转染的细胞中检测到的非感染性芽生病毒水平较低,这是通过 Q-PCR 检测病毒 DNA 或通过免疫印迹检测芽生病毒蛋白来检测的。因此,ac109 的缺失影响核内核衣壳的包被和感染性芽生病毒的产生。