感染质多角体病毒-23的 Sf9 细胞的转录分析
Transcriptional Analysis of Sf9 Cells Infected with Cypovirus-23.
作者信息
Kuang Wendong, Yang Jian, Wang Jinchang, Yan Chenghua, Chen Junhui, Liu Xinsheng, Yang Chunhua, Zhan Zhigao, Guan Limei, Li Jianghuai, Deng Tao, Yang Feiying, Ma Guangqiang, Jin Liang
机构信息
Institute of Microbiology, Jiangxi Academy of Sciences, Nanchang 330029, China.
Institute of Biological Resources, Jiangxi Academy of Sciences, Nanchang 330029, China.
出版信息
Int J Mol Sci. 2025 Aug 2;26(15):7487. doi: 10.3390/ijms26157487.
cypovirus-23 (DnCPV-23) is a new type of cypovirus that has a lethal effect on many species of Sphingidae pests. DnCPV-23 can replicate in Sf9 cells, but the replication characteristics of the virus in this cell line are still unclear. To determine the replication characteristics of DnCPV-23 in Sf9 cells, uninfected Sf9 cells and Sf9 cells at 24 and 72 h after DnCPV-23 infection were collected for transcriptome analysis. Compared to uninfected Sf9 cells, a total of 188 and 595 differentially expressed genes (DEGs) were identified in Sf9 cells collected at 24 hpi and 72 h, respectively. KEGG analyses revealed that 139 common DEGs in two treatment groups were related to nutrition and energy metabolism-related processes, cell membrane integrity and function-related pathways, detoxification-related pathways, growth and development-related pathways, and so on. We speculated that these cellular processes might be manipulated by viruses to promote replication. This study provides an important basis for further in-depth research on the mechanism of interaction between viruses and hosts. It provides additional basic information for the future exploitation of DnCPV-23 as a biological insecticide.
质型多角体病毒-23(DnCPV-23)是一种新型质型多角体病毒,对多种天蛾科害虫具有致死作用。DnCPV-23可在Sf9细胞中复制,但该病毒在这种细胞系中的复制特性仍不清楚。为了确定DnCPV-23在Sf9细胞中的复制特性,收集未感染的Sf9细胞以及感染DnCPV-23后24小时和72小时的Sf9细胞用于转录组分析。与未感染的Sf9细胞相比,在感染后24小时和72小时收集的Sf9细胞中分别鉴定出总共188个和595个差异表达基因(DEG)。KEGG分析表明,两个处理组中的139个共同DEG与营养和能量代谢相关过程、细胞膜完整性和功能相关途径、解毒相关途径、生长和发育相关途径等有关。我们推测这些细胞过程可能被病毒操纵以促进复制。本研究为进一步深入研究病毒与宿主之间的相互作用机制提供了重要依据。它为未来将DnCPV-23开发为生物杀虫剂提供了额外的基础信息。