Rivkin Hadassah, Kroemer Jeremy A, Bronshtein Alexander, Belausov Eduard, Webb Bruce A, Chejanovsky Nor
Entomology Department, Institute of Plant Protection, The Volcani Center, POB 6, Bet Dagan 50250, Israel.
Department of Entomology, University of Kentucky, S-225 Agricultural Sciences Center North, Lexington, KY 40546, USA.
J Gen Virol. 2006 Aug;87(Pt 8):2217-2225. doi: 10.1099/vir.0.81918-0.
The Mediterranean lepidopteran pest Spodoptera littoralis is highly resistant to infection with the Autographa californica multiple nucleopolyhedrovirus (AcMNPV) via the oral route, but highly sensitive to infection with budded virus (BV) via the intrahaemocoelic route. To study the fate of AcMNPV infection in S. littoralis, vHSGFP, an AcMNPV recombinant that expresses the reporter green fluorescent protein gene under the control of the Drosophila heat-shock promoter, and high-resolution fluorescence microscopy were utilized. S. littoralis fourth-instar larvae infected orally with vHSGFP showed melanization and encapsulation of virus-infected tracheoblast cells serving the midgut columnar cells. At 72 h post-infection, the viral foci were removed during the moult clearing the infection. Thus, oral infection was restricted by immune responses to the midgut and midgut-associated tracheal cells. By contrast, injection of BV into the haemocoel resulted in successful infection of tracheoblasts, followed by spread of the virus through the tracheal epidermis to other tissues. However, in contrast to fully permissive infections where tracheoblasts and haemocytes are equally susceptible to infection, a severe limitation to vHSGFP infection of haemocytes was observed. To investigate the resistance of S. littoralis haemocytes to BV infection with AcMNPV, the larval immune system was suppressed with the Chelonus inanitus polydnavirus or a putatively immunosuppressive polydnavirus gene, P-vank-1. Both treatments increased the susceptibility of S. littoralis larvae to AcMNPV. It is concluded that the resistance of S. littoralis to AcMNPV infection involves both humoral and cellular immune responses that act at the gut and haemocyte levels. The results also support the hypothesis that tracheolar cells mediate establishment of systemic baculovirus infections in lepidopteran larvae. The finding that polydnaviruses and their encoded genes synergize baculovirus infection also provides an approach to dissecting the responses of the lepidopteran immune system to viruses by using specific polydnavirus immunosuppressive genes.
地中海鳞翅目害虫草地贪夜蛾对经口感染苜蓿银纹夜蛾多核多角体病毒(AcMNPV)具有高度抗性,但对经血腔途径感染出芽病毒(BV)高度敏感。为了研究AcMNPV在草地贪夜蛾中的感染命运,利用了vHSGFP(一种在果蝇热休克启动子控制下表达报告绿色荧光蛋白基因的AcMNPV重组体)和高分辨率荧光显微镜。经口感染vHSGFP的草地贪夜蛾四龄幼虫显示,为中肠柱状细胞提供服务的病毒感染气管母细胞出现黑化和包囊现象。感染后72小时,在蜕皮过程中病毒病灶被清除,感染得以消除。因此,经口感染受到对中肠和中肠相关气管细胞的免疫反应的限制。相比之下,将BV注入血腔会导致气管母细胞成功感染,随后病毒通过气管表皮扩散到其他组织。然而,与气管母细胞和血细胞对感染同样敏感的完全允许感染不同,观察到血细胞对vHSGFP感染存在严重限制。为了研究草地贪夜蛾血细胞对AcMNPV感染BV的抗性,用斜纹夜蛾多角体病毒或一个假定的免疫抑制多角体病毒基因P-vank-1抑制幼虫免疫系统。两种处理都增加了草地贪夜蛾幼虫对AcMNPV的易感性。得出的结论是,草地贪夜蛾对AcMNPV感染的抗性涉及在肠道和血细胞水平起作用的体液免疫和细胞免疫反应。结果还支持气管细胞介导鳞翅目幼虫系统性杆状病毒感染建立的假说。多角体病毒及其编码基因协同杆状病毒感染的发现,也为利用特定的多角体病毒免疫抑制基因剖析鳞翅目免疫系统对病毒的反应提供了一种方法。