Li Qianjun, Liston Peter, Moyer Richard W
Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville, FL 32610-0266, USA.
J Virol. 2005 Feb;79(4):2335-45. doi: 10.1128/JVI.79.4.2335-2345.2005.
The entomopoxvirus from Amsacta moorei (AmEPV) contains none of the commonly recognized vertebrate poxvirus apoptotic suppressor genes. However, AmEPV carries a single inhibitor of apoptosis (iap) gene (AMViap) not present in vertebrate poxviruses. The AMViap gene was active when coexpressed with the Drosophila proapoptotic gene hid in Ld652 cells and can rescue cells from apoptosis as shown by increased number of surviving cells and reduced levels of caspase-3-like activity. We also showed that expression of the AMViap gene rescued polyhedron production in Autographa californica M nucleopolyhedrovirus (AcMNPV)Deltap35-infected Sf9 cells during an otherwise abortive infection induced by apoptosis. Surprisingly, deletion of the AMViap gene from the AmEPV genome led to only a modest (10-fold) loss of virion production in infected Ld652 cells, indicating that the AMViap gene is nonessential for virus replication under these conditions. However, infection of Ld652 cells by AmEPV lacking a functional iap gene led to a more rapid induction of cytotoxicity and increased levels of caspase-3-like activity. Similar results were observed and were more pronounced in infected Sf9 and S2 cells. The purified AMVIAP protein also inhibits the enzymatic activities of human caspase-9 and caspase-3 in vitro. Our results indicate that while the AMViap gene was active in controlling apoptosis through the intrinsic pathway, the virus likely encodes additional proteins that also regulate apoptosis.
来自摩尔粘虫(Amsacta moorei)的昆虫痘病毒(AmEPV)不包含任何常见的脊椎动物痘病毒凋亡抑制基因。然而,AmEPV携带一个脊椎动物痘病毒中不存在的凋亡抑制基因(iap)(AMViap)。当与果蝇促凋亡基因hid在Ld652细胞中共表达时,AMViap基因具有活性,并且如存活细胞数量增加和半胱天冬酶-3样活性水平降低所示,它可以拯救细胞免于凋亡。我们还表明,在由凋亡诱导的原本失败的感染过程中,AMViap基因的表达挽救了苜蓿银纹夜蛾多核型多角体病毒(AcMNPV)Δp35感染的Sf9细胞中的多角体产生。令人惊讶的是,从AmEPV基因组中缺失AMViap基因仅导致感染的Ld652细胞中病毒粒子产生适度(10倍)的损失,这表明在这些条件下AMViap基因对于病毒复制并非必需。然而,缺乏功能性iap基因的AmEPV感染Ld652细胞会导致细胞毒性更快诱导和半胱天冬酶-3样活性水平增加。在感染的Sf9和S2细胞中观察到了类似的结果,并且更为明显。纯化的AMVIAP蛋白在体外也抑制人半胱天冬酶-9和半胱天冬酶-3的酶活性。我们的结果表明,虽然AMViap基因在通过内在途径控制凋亡方面具有活性,但该病毒可能还编码其他调节凋亡的蛋白质。