Yu Dong-Shuai, Chen Ya-Bin, Li Ming, Yang Ming-Jun, Yang Yang, Hu Jian-Sheng, Luo Kai-Jun
Key Laboratory for Animal Genetic Diversity and Evolution of High Education in Yunnan Province, School of Life Sciences, Yunnan University, Kunming, 650091, People's Republic of China.
Shanghai-MOST Key Laboratory of Health and Disease Genomic, Chinese National Human Genome Center at Shanghai, Shanghai, 201203, People's Republic of China.
Arch Virol. 2016 Nov;161(11):3095-124. doi: 10.1007/s00705-016-2988-3. Epub 2016 Aug 13.
Polydnaviruses (PDVs) play a critical role in altering host gene expression to induce immunosuppression. However, it remains largely unclear how PDV genes affect host genes. Here, the complete genome sequence of Microplitis bicoloratus bracovirus (MbBV), which is known to be an apoptosis inducer, was determined. The MbBV genome consisted of 17 putative double-stranded DNA circles and 179 fragments with a total size of 336,336 bp and contained 116 open reading frames (ORFs). Based on conserved domains, nine gene families were identified, of which the IκB-like viral ankyrin (vank) family included 28 members and was one of the largest families. Among the 116 ORFs, 13 MbBV genes were expressed in hemocytes undergoing MbBV-induced apoptosis and further analyzed. Three vank genes (vank86, vank92, vank101) were expressed in hemocytes collected from Spodoptera litura larvae parasitized by M. bicoloratus, in which host NF-κB/IκBs, including relish, dorsal, and cactus, were also persistently expressed. When Spli221 cells were infected with MbBV viral particles, mRNA levels of host and viral NF-κB/IκB genes were persistent and also varied in Spli221 cells undergoing virus-induced pre-apoptosis cell from 1 to 5 hours postinfection. Both were then expressed in a time-dependent expression in virus-induced apoptotic cells. These data show that viral IκB-like transcription does not inhibit host NF-κB/IκB expression, suggesting that transcription of these genes might be regulated by different mechanisms.
多分DNA病毒(PDVs)在改变宿主基因表达以诱导免疫抑制方面发挥着关键作用。然而,PDV基因如何影响宿主基因在很大程度上仍不清楚。在此,测定了已知为凋亡诱导剂的双色微颚茧蜂杆状病毒(MbBV)的完整基因组序列。MbBV基因组由17个推定的双链DNA环和179个片段组成,总大小为336,336 bp,包含116个开放阅读框(ORFs)。基于保守结构域,鉴定出9个基因家族,其中类IκB病毒锚蛋白(vank)家族包括28个成员,是最大的家族之一。在116个ORFs中,13个MbBV基因在经历MbBV诱导凋亡的血细胞中表达并进一步分析。3个vank基因(vank86、vank92、vank101)在被双色微颚茧蜂寄生的斜纹夜蛾幼虫采集的血细胞中表达,其中包括 relish、dorsal和cactus在内的宿主NF-κB/IκBs也持续表达。当Spli221细胞用MbBV病毒颗粒感染时,宿主和病毒NF-κB/IκB基因的mRNA水平持续存在,并且在感染后1至5小时经历病毒诱导的凋亡前期细胞的Spli221细胞中也有所变化。然后两者在病毒诱导的凋亡细胞中均呈时间依赖性表达。这些数据表明,病毒类IκB转录并不抑制宿主NF-κB/IκB表达,提示这些基因的转录可能受不同机制调控。