Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha, Hunan, China.
College of Plant Protection, Hunan Agricultural University, Changsha, Hunan, China.
mBio. 2023 Feb 28;14(1):e0311922. doi: 10.1128/mbio.03119-22. Epub 2023 Feb 6.
Ascoviruses are insect-specific viruses thought to utilize the cellular apoptotic processes of host larvae to produce numerous virion-containing vesicles. In this study, we first determined the biochemical characteristics of ascovirus-infected, cultured insect cells and the possible antiapoptotic capacity of ascovirus-infected insect cells. The results indicated that the ascovirus infection in the first 24 h was different from the infection from 48 h to the later infection stages. In the early infection stage, the Spodoptera exigua host cells had high membrane permeability and cleaved gasdermin D (GSDMD) but uncleaved Casp-6 (SeCasp-6). In contrast, the later infection stage had no such increased membrane permeability and had cleaved SeCasp-6. Four different chemicals were used to induce apoptosis at different stages of ascovirus infection: hydrogen peroxide (HO) and actinomycin D (ActD) had similar effects on the ascovirus-infected cells, whereas cMYC inhibitors and tumor necrosis factor alpha (TNF-α) plus SM-164 apoptosis inducers (T/S) had similar effects on infected cells. The former two inducers inhibited viral DNA replication in most situations, while the latter two inducers inhibited viral DNA replication in the early stage of infection but promoted viral DNA replication in the later infection stage. Furthermore, immunoblotting assays verified that T/S treatment could increase the expression levels of viral major capsid protein (MCP) and the host inhibitor of apoptosis protein (SeIAP). Coimmunoprecipitation assays revealed interaction between SeIAP and SeCasps, but this interaction was disturbed in ascovirus-infected cells. This study details the infection process of ascovirus, indicating the utilization of pyroptosis for antiapoptosis cytopathology. Clarifying the relationship between different types of viral infections and host regulation of cell death (RCD) can provide insights into the interaction between viruses and host cells. Ascoviruses are insect-specific viruses with apoptosis-utilizing-like infection cytopathology. However, RCD does not only include apoptosis, and while in our previous transmission electron microscopic observations, ascovirus-infected cells did not show typical apoptotic characteristics (unpublished data), in this study, they did show increased membrane permeability. These results indicate that the cytopathology of ascovirus infection is a complex process in which the virus manipulates host RCD. The RCD of insect cells is quite different from that of mammals, and studies on the former are many fewer than those on the latter, especially in the case of RCD in lepidopteran insects. Our results will lay a foundation for understanding the RCD of lepidopteran insects and its function in the process of insect virus infection.
杆状病毒是一种特异性感染昆虫的病毒,被认为利用宿主幼虫的细胞凋亡过程产生大量含有病毒粒子的小泡。在本研究中,我们首先确定了杆状病毒感染的培养昆虫细胞的生化特征,以及杆状病毒感染的昆虫细胞可能的抗凋亡能力。结果表明,杆状病毒在感染的前 24 小时与 48 小时后的感染阶段不同。在早期感染阶段,斜纹夜蛾(Spodoptera exigua)宿主细胞具有较高的膜通透性和裂解的 gasdermin D(GSDMD),但未裂解的 Casp-6(SeCasp-6)。相比之下,后期感染阶段没有增加的膜通透性,且裂解了 SeCasp-6。在不同的杆状病毒感染阶段,使用四种不同的化学物质诱导细胞凋亡:过氧化氢(HO)和放线菌素 D(ActD)对杆状病毒感染的细胞有相似的作用,而 cMYC 抑制剂和肿瘤坏死因子 alpha(TNF-α)加 SM-164 凋亡诱导剂(T/S)对感染的细胞有相似的作用。前两种诱导剂在大多数情况下抑制病毒 DNA 的复制,而后两种诱导剂在感染的早期阶段抑制病毒 DNA 的复制,但在后期感染阶段促进病毒 DNA 的复制。此外,免疫印迹分析验证了 T/S 处理可以增加病毒主要衣壳蛋白(MCP)和宿主凋亡抑制蛋白(SeIAP)的表达水平。免疫共沉淀分析显示 SeIAP 和 SeCasps 之间存在相互作用,但这种相互作用在杆状病毒感染的细胞中受到干扰。本研究详细描述了杆状病毒的感染过程,表明其利用细胞焦亡进行抗凋亡细胞病理学。阐明不同类型病毒感染与宿主细胞死亡调控(RCD)之间的关系,可以深入了解病毒与宿主细胞之间的相互作用。杆状病毒是一种特异性感染昆虫的病毒,具有利用细胞凋亡的感染细胞病理学。然而,RCD 并不仅限于细胞凋亡,并且在我们之前的透射电子显微镜观察中,杆状病毒感染的细胞没有表现出典型的凋亡特征(未发表的数据),但在本研究中,它们确实表现出了增加的膜通透性。这些结果表明,杆状病毒感染的细胞病理学是一个复杂的过程,病毒操纵宿主 RCD。昆虫细胞的 RCD 与哺乳动物有很大的不同,而且对前者的研究比后者少得多,特别是在鳞翅目昆虫的 RCD 方面。我们的研究结果将为理解鳞翅目昆虫的 RCD 及其在昆虫病毒感染过程中的功能奠定基础。