Lapointe Renée, Wilson Rebecca, Vilaplana Lluïsa, O'Reilly David R, Falabella Patrizia, Douris Vassilis, Bernier-Cardou Michèle, Pennacchio Francesco, Iatrou Kostas, Malva Carla, Olszewski Julie A
Department of Biological Sciences, Imperial College, London SW7 2AZ, UK.
Dipartimento di Biologia, Difesa e Biotecnologie, Agro-Forestali-Università della Basilicata-Macchia Romana, 85100 Potenza, Italy.
J Gen Virol. 2005 Apr;86(Pt 4):963-971. doi: 10.1099/vir.0.80834-0.
The polydnavirus Toxoneuron nigriceps bracovirus (TnBV) is an obligate symbiont associated with the braconid wasp T. nigriceps, a parasitoid of Heliothis virescens larvae. Previously, to identify polydnavirus genes that allow parasitization by altering the host immune and endocrine systems, expression patterns of TnBV genes from parasitized H. virescens larvae were analysed and cDNAs were obtained. To study the function of the protein from one such cDNA, TnBV1, overexpression of the protein was attempted by using the baculovirus Autographa californica multicapsid nucleopolyhedrovirus. Recovery of stable recombinant virus was unsuccessful, with the exception of recombinants with deletions/mutations within the TnBV1 gene. It was hypothesized that TnBV1 expression was cytotoxic to the Spodoptera frugiperda (Sf21) insect cells that were used to produce the recombinants. Therefore, the Bac-to-Bac system was used to create recombinant baculoviruses maintained in Escherichia coli expressing either TnBV1 (Ac-TnBV1) or an initiator-methionine mutant [Ac-TnBV1(ATG-)]. Microscopy revealed substantial cell death of Sf21 and High Five cells from 48 h post-infection with Ac-TnBV1, but not with the Ac-TnBV1(ATG-) recombinant virus. Ac-TnBV1-infected Sf21 cells, but not those with parental virus infection, showed an increased caspase-3-like protease activity, as well as increased terminal deoxynucleotidyltransferase-mediated dUTP nick-end labelling (TUNEL) for breaks in host genomic DNA. Although indicative of apoptosis, blebbing and apoptotic bodies were not observed in infected cells. Transiently expressing TnBV1 alone caused TUNEL staining in High Five cells. These data suggest that TnBV1 expression alone can induce apoptosis-like programmed cell death in two insect cell lines. Injection of Ac-TnBV1 budded virus, compared with parental virus, did not result in an alteration of virulence in H. virescens larvae.
多DNA病毒黑头酸浆斑痣悬茧蜂杆状病毒(TnBV)是一种专性共生体,与茧蜂科昆虫黑头酸浆斑痣悬茧蜂相关,后者是棉铃虫幼虫的寄生蜂。此前,为了鉴定通过改变宿主免疫和内分泌系统来实现寄生的多DNA病毒基因,分析了来自被寄生的棉铃虫幼虫的TnBV基因的表达模式并获得了cDNA。为了研究来自其中一个这样的cDNA(TnBV1)的蛋白质的功能,尝试使用苜蓿银纹夜蛾多粒包埋核型多角体病毒通过杆状病毒来过表达该蛋白质。除了TnBV1基因内有缺失/突变的重组体之外,稳定重组病毒的回收未成功。据推测,TnBV1的表达对用于生产重组体的草地贪夜蛾(Sf21)昆虫细胞具有细胞毒性。因此,使用杆状病毒表达系统来创建在表达TnBV1(Ac-TnBV1)或起始甲硫氨酸突变体[Ac-TnBV1(ATG-)]的大肠杆菌中维持的重组杆状病毒。显微镜检查显示,感染Ac-TnBV1后48小时,Sf21和High Five细胞出现大量细胞死亡,但感染Ac-TnBV1(ATG-)重组病毒的细胞未出现这种情况。感染Ac-TnBV1的Sf21细胞,而非感染亲本病毒的细胞,显示出类似半胱天冬酶-3的蛋白酶活性增加,以及宿主基因组DNA断裂的末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)增加。尽管表明存在凋亡,但在感染细胞中未观察到细胞起泡和凋亡小体。单独瞬时表达TnBV1会导致High Five细胞出现TUNEL染色。这些数据表明,单独的TnBV1表达可在两种昆虫细胞系中诱导凋亡样程序性细胞死亡。与亲本病毒相比,注射Ac-TnBV1出芽病毒不会导致棉铃虫幼虫的毒力改变。