Functional analysis of the Autographa californica nucleopolyhedrovirus IAP1 and IAP2.

XianDong Zeng, Fang Nan, ChangYong Liang, JianHua Song, Qian Wang, Just M Vlak, XinWen Chen
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引用次数: 22

Abstract

The Autographa californica nucleopolyhedrovirus (AcMNPV) contains three apoptosis suppressor genes: p35, iap1 and iap2. AcMNPV P35 functions as a pancaspase inhibitor, but the function of IAP1 and IAP2 has not been entirely resolved. In this paper, we analyze the function of IAP1 and IAP2 in detail. AcMNPV with p35-deletion inhibited the apoptosis of BTI-Tn-5B1-4 (Tn-Hi5) cells induced by a Helicoverpa armigera single nucleocapsid NPV (HearNPV) infection and rescued the replication of HearNPV and BV production in these cells. Transient-expression experiments indicated that both IAP1 and IAP2 suppress apoptosis of Tn-Hi5 cells during HearNPV infection. Recombinant HearNPVs expressing AcMNPV iap1, iap2 and p35, respectively, not only prevented apoptosis but also allowed HearNPV to replicate in Tn-Hi5 cells. However, the iap1, iap2 and p35 genes when expressed in HearNPV were unable to rescue BV production. These results indicate that both AcMNPV iap1 and iap2 function independently as apoptosis inhibitors of and are potential host range factors.

加州签名蝇核多角体病毒IAP1和IAP2的功能分析。
加州自签名核多角体病毒(AcMNPV)含有3个凋亡抑制基因:p35、iap1和iap2。AcMNPV P35作为pancaspase抑制剂,但IAP1和IAP2的功能尚未完全解决。本文详细分析了IAP1和IAP2的功能。缺失p35的AcMNPV抑制了棉铃虫单核衣壳NPV (HearNPV)感染诱导的BTI-Tn-5B1-4 (Tn-Hi5)细胞的凋亡,挽救了这些细胞的HearNPV复制和BV的产生。瞬时表达实验表明,IAP1和IAP2均可抑制肝病毒感染时Tn-Hi5细胞的凋亡。分别表达AcMNPV iap1、iap2和p35的重组HearNPV不仅能阻止细胞凋亡,还能使HearNPV在Tn-Hi5细胞中复制。然而,当iap1、iap2和p35基因在HearNPV中表达时,无法挽救BV的产生。这些结果表明,AcMNPV iap1和iap2作为凋亡抑制剂独立发挥作用,是潜在的宿主范围因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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