Duffy Simon P, Becker Elisa M, Whittome Beatrixe H, Lucarotti Christopher J, Levin David B
The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
Department of Biology, University of Victoria, Victoria, BC V8W 2Y2, Canada.
J Gen Virol. 2007 Jul;88(Pt 7):1945-1951. doi: 10.1099/vir.0.82763-0.
DNA replication and transcription of NeabNPV, the nucleopolyhedrovirus (NPV) of the balsam fir sawfly, Neodiprion abietis (Hymenoptera: Diprionidae), in host larvae were investigated. NPV DNA replication kinetics and gene-expression patterns have been resolved only in lepidopteran cell-culture systems and in limited in vivo experiments with lepidopteran larvae. Furthermore, there are significant differences in pathologies caused by lepidopteran NPVs, which replicate in many tissues, and hymenopteran NPVs, known to replicate in midgut epithelium only. Despite the differences in host specificity and pathology, NeabNPV DNA replication kinetics were similar to those reported for lepidopteran NPVs. Maximal NeabNPV DNA synthesis was observed between 4 and 24 h post-inoculation (p.i.) but, in contrast to lepidopteran NPVs, synthesis continued at a lower rate up to 72 h p.i. Selected NeabNPV genes exhibited a cascade pattern of transcription similar to that of lepidopteran NPVs. RT-PCR products of the NeabNPV lef-1, lef-2 and dnapol transcripts were observed as early as 2 h p.i., whilst lef-8 and lef-9, encoding putative viral RNA polymerase subunits, were detected at 1 and 6 h p.i., respectively. Two structural late transcripts (gp41 and p74) were observed from 6 h p.i. The very late factor 1 (vlf-1) transcript, a transactivator of very late genes, was observed from 12 h p.i., but the very late transcript polh, encoding the major occlusion protein, polyhedrin, was observed from 24 h p.i. This study provides the first insight into DNA replication and gene expression of a non-lepidopteran baculovirus.
对香脂冷杉叶蜂(Neodiprion abietis,膜翅目:叶蜂科)的核多角体病毒(NPV)——NeabNPV在宿主幼虫中的DNA复制和转录进行了研究。NPV DNA复制动力学和基因表达模式仅在鳞翅目细胞培养系统以及对鳞翅目幼虫进行的有限体内实验中得到解析。此外,在许多组织中复制的鳞翅目NPV与仅在中肠上皮中复制的膜翅目NPV所引起的病理学存在显著差异。尽管宿主特异性和病理学存在差异,但NeabNPV的DNA复制动力学与报道的鳞翅目NPV相似。在接种后4至24小时观察到NeabNPV DNA合成达到最大值,但与鳞翅目NPV不同的是,合成以较低速率持续至接种后72小时。所选的NeabNPV基因表现出与鳞翅目NPV相似的转录级联模式。NeabNPV lef-1、lef-2和dnapol转录本的RT-PCR产物最早在接种后2小时观察到,而编码假定病毒RNA聚合酶亚基的lef-8和lef-9分别在接种后1小时和6小时检测到。从接种后6小时观察到两种结构晚期转录本(gp41和p74)。极晚期因子1(vlf-1)转录本,一种极晚期基因的反式激活因子,从接种后12小时观察到,但编码主要包涵体蛋白多角体蛋白的极晚期转录本polh从接种后24小时观察到。本研究首次深入了解了非鳞翅目杆状病毒的DNA复制和基因表达。