Department of Entomology, The Pennsylvania State University, 501 ASI, University Park, PA 16802, USA.
J Gen Virol. 2010 Jun;91(Pt 6):1590-600. doi: 10.1099/vir.0.018952-0. Epub 2010 Feb 17.
Lymantria dispar has a long historical association with the baculovirus Lymantria dispar multiple nucleopolyhedrovirus (LdMNPV), which is one of the primary population regulators of L. dispar in the field. However, host larvae exhibit strong developmental resistance to fatal infection by LdMNPV; the LD50 in newly moulted fourth instars is 18-fold lower than in the middle of the instar (48-72 h post-moult). Using a recombinant of LdMNPV expressing lacZ, we examined the key steps of pathogenesis in the host to explore mechanisms of developmental resistance. At the midgut level, we observed reduced primary midgut infections in mid-fourth instars, indicating increased sloughing of infected cells. Additional barriers were observed as the virus escaped the midgut. Mid-fourth instars had higher numbers of melanized foci of infection associated with the midgut, apoptotic tracheal epidermal cells and haemocytes, and reduced numbers of infected haemocytes later in infection. Our results show that the co-evolutionary relationship between L. dispar and LdMNPV has resulted in both midgut-based and systemic antiviral defences and that these defences are age-dependent within the instar. This age-related susceptibility may contribute to how the virus is maintained in nature and could influence management of L. dispar by using the virus.
舞毒蛾与杆状病毒舞毒蛾多核多角体病毒(LdMNPV)有着悠久的历史联系,该病毒是舞毒蛾在野外的主要种群调节因子之一。然而,宿主幼虫对致命的 LdMNPV 感染表现出强烈的发育抗性;新蜕皮的第四龄幼虫的 LD50 比蜕皮中期(蜕皮后 48-72 小时)低 18 倍。我们使用表达 lacZ 的 LdMNPV 重组体,研究了宿主发病机制的关键步骤,以探索发育抗性的机制。在中肠水平,我们观察到第四龄中期的原发性中肠感染减少,表明感染细胞的脱落增加。随着病毒从中肠逃脱,观察到了其他的障碍。第四龄中期与中肠相关的感染黑色素焦点、凋亡的气管表皮细胞和血细胞数量增加,感染的血细胞数量在感染后期减少。我们的研究结果表明,舞毒蛾和 LdMNPV 之间的共同进化关系导致了基于中肠的和系统的抗病毒防御,并且这些防御在龄内是年龄依赖性的。这种与年龄相关的易感性可能有助于解释病毒在自然界中的维持方式,并可能影响利用该病毒来管理舞毒蛾。