Gundersen-Rindal D E, Pedroni M J
US Department of Agriculture, Agricultural Research Service, Insect Biocontrol Laboratory, Bldg 011A, Room 214, BARC West, Beltsville, MD 20705, USA.
J Gen Virol. 2006 Feb;87(Pt 2):311-322. doi: 10.1099/vir.0.81326-0.
Glyptapanteles indiensis (Braconidae, Hymenoptera) is an endoparasitoid of Lymantria dispar, the gypsy moth. Expression of G. indiensis polydnavirus (GiBV)-encoded genes within the pest host results in inhibition of immune response and development and alteration of physiology, enabling successful development of the parasitoid. Here, GiBV genome segment F (segF), an 18.6 kb segment shown to encode nine protein tyrosine phosphatase (PTP) genes and a single ankyrin repeat gene (ank), is analysed. PTPs have presumed function as regulators of signal transduction, while ankyrin repeat genes are hypothesized to function in inhibition of NF-kappaB signalling in the parasitized host. In this study, transcription of each gene was mapped by 5'- and 3'-RACE (rapid amplification of cDNA ends) and temporal and tissue-specific expression was examined in the parasitized host. For polydnavirus gene prediction in the parasitized host, no available gene prediction parameters were entirely precise. The mRNAs for each GiBV segF gene initiated between 30 and 112 bp upstream of the translation initiation codon. All were encoded in single open reading frames (ORFs), with the exception of PTP9, which was transcribed as a bicistronic message with the adjacent ank gene. RT-PCR indicated that all GiBV segF PTPs were expressed early in parasitization and, for most, expression was sustained over the course of at least 7 days after parasitization, suggesting importance in both early and sustained virus-induced immunosuppression and alteration of physiology. Tissue-specific patterns of PTP expression of GiBV segF genes were variable, suggesting differing roles in facilitating parasitism.
印度刻绒茧蜂(茧蜂科,膜翅目)是舞毒蛾的一种内寄生蜂。印度刻绒茧蜂多角体病毒(GiBV)编码基因在害虫宿主体内的表达会导致免疫反应和发育受到抑制以及生理状态改变,从而使寄生蜂能够成功发育。在此,对GiBV基因组片段F(segF)进行了分析,该片段长18.6 kb,已显示编码9个蛋白酪氨酸磷酸酶(PTP)基因和1个锚蛋白重复基因(ank)。PTP被推测具有作为信号转导调节因子的功能,而锚蛋白重复基因被假设在被寄生宿主中抑制NF-κB信号传导发挥作用。在本研究中,通过5'-和3'-RACE(cDNA末端快速扩增)对每个基因的转录进行了定位,并在被寄生宿主中检测了其时间和组织特异性表达。对于被寄生宿主中的多角体病毒基因预测,没有可用的基因预测参数是完全精确的。每个GiBV segF基因的mRNA在翻译起始密码子上游30至112 bp之间起始。所有基因均编码在单个开放阅读框(ORF)中,但PTP9除外,它与相邻的ank基因转录为双顺反子信息。RT-PCR表明,所有GiBV segF PTPs在寄生早期表达,并且大多数在寄生后至少7天内持续表达,这表明它们在早期和持续的病毒诱导的免疫抑制以及生理改变中都很重要。GiBV segF基因的PTP表达的组织特异性模式各不相同,表明在促进寄生方面具有不同的作用。