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NS1 Protein of Influenza A Virus Down-Regulates Apoptosis

机译:甲型流感病毒的NS1蛋白下调细胞凋亡

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摘要

Wild-type (WT) influenza A/PR/8/34 virus and its variant lacking the NS1 gene (delNS1) have been compared for their ability to mediate apoptosis in cultured cells and chicken embryos. Cell morphology, fragmentation of chromatin DNA, and caspase-dependent cleavage of the viral NP protein have been used as markers for apoptosis. Another marker was caspase cleavage of the viral M2 protein, which was also found to occur in an apoptosis-specific manner. In interferon (IFN)-competent host systems, such as MDCK cells, chicken fibroblasts, and 7-day-old chicken embryos, delNS1 virus induced apoptosis more rapidly and more efficiently than WT virus. As a consequence, delNS1 virus was also more lethal for chicken embryos than WT virus. In IFN-deficient Vero cells, however, apoptosis was delayed and developed with similar intensity after infection with both viruses. Taken together, these data indicate that the IFN antagonistic NS1 protein of influenza A viruses has IFN-dependent antiapoptotic potential.
机译:已经比较了野生型(WT)流感A / PR / 8/34病毒及其缺少NS1基因(delNS1)的变异体介导培养细胞和鸡胚凋亡的能力。细胞形态,染色质DNA片段化以及病毒NP蛋白的caspase依赖性切割已被用作凋亡的标志物。另一个标志是病毒M2蛋白的半胱天冬酶裂解,也发现它以凋亡特异性方式发生。在具有干扰素(IFN)功能的宿主系统中,例如MDCK细胞,鸡成纤维细胞和7天大的鸡胚,与WT病毒相比,delNS1病毒诱导凋亡的速度更快,效率更高。因此,与WT病毒相比,delNS1病毒对鸡胚的致命性也更高。但是,在缺乏IFN的Vero细胞中,两种病毒感染后,凋亡均被延迟并以相似的强度发展。综上所述,这些数据表明甲型流感病毒的IFN拮抗性NS1蛋白具有IFN依赖性的抗凋亡潜力。

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