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禽呼肠孤病毒可在培养细胞中诱导凋亡:诱导凋亡需要病毒脱壳,但不需要病毒基因表达。

Avian reoviruses cause apoptosis in cultured cells: viral uncoating, but not viral gene expression, is required for apoptosis induction.

作者信息

Labrada Lucía, Bodelón Gustavo, Viñuela Juan, Benavente Javier

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain.

出版信息

J Virol. 2002 Aug;76(16):7932-41. doi: 10.1128/jvi.76.16.7932-7941.2002.

Abstract

The cytopathic effect evidenced by cells infected with avian reovirus S1133 suggests that this virus may induce apoptosis in primary cultures of chicken embryo fibroblasts. In this report we present evidence that avian reovirus infection of cultured cells causes activation of the intracellular apoptotic program and that this activation takes place during an early stage of the viral life cycle. The ability of avian reoviruses to induce apoptosis is not restricted to a particular virus strain or to a specific cell type, since different avian reovirus isolates were able to induce apoptosis in several avian and mammalian cell lines. Apoptosis was also provoked in ribavirin-treated avian reovirus-infected cells and in cells infected with UV-irradiated reovirions, indicating that viral mRNA synthesis and subsequent steps in viral replication are not needed for apoptosis induction in avian reovirus-infected cells and that the number of inoculated virus particles, not their infectivity, is the critical factor for apoptosis induction by avian reovirus. Our finding that apoptosis is no longer induced when intracellular viral uncoating is blocked indicates that intraendosomal virion disassembly is required for apoptosis induction and that attachment and uptake of parental reovirions are not sufficient to cause apoptosis. Taken together, our results suggest that apoptosis is triggered from within the infected cell by viral products generated after intraendosomal uncoating of parental reovirions.

摘要

感染禽呼肠孤病毒S1133的细胞所表现出的细胞病变效应表明,该病毒可能在鸡胚成纤维细胞原代培养物中诱导细胞凋亡。在本报告中,我们提供证据表明,培养细胞感染禽呼肠孤病毒会导致细胞内凋亡程序的激活,且这种激活发生在病毒生命周期的早期阶段。禽呼肠孤病毒诱导细胞凋亡的能力并不局限于特定的病毒株或特定的细胞类型,因为不同的禽呼肠孤病毒分离株能够在多种禽类和哺乳动物细胞系中诱导细胞凋亡。利巴韦林处理的感染禽呼肠孤病毒的细胞以及感染紫外线照射的呼肠孤病毒粒子的细胞也会引发细胞凋亡,这表明禽呼肠孤病毒感染的细胞诱导细胞凋亡不需要病毒mRNA合成及病毒复制的后续步骤,且接种的病毒粒子数量而非其感染性是禽呼肠孤病毒诱导细胞凋亡的关键因素。我们的研究发现,当细胞内病毒脱壳被阻断时不再诱导细胞凋亡,这表明内体病毒粒子解体是诱导细胞凋亡所必需的,且亲本呼肠孤病毒粒子的附着和摄取不足以导致细胞凋亡。综上所述,我们的结果表明,细胞凋亡是由亲本呼肠孤病毒粒子在内体脱壳后产生的病毒产物在受感染细胞内触发的。

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