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Nonstructural Protein of Infectious Bursal Disease Virus Inhibits Apoptosis at the Early Stage of Virus Infection

机译:传染性法氏囊病病毒的非结构蛋白在病毒感染的早期抑制细胞凋亡。

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摘要

Infectious bursal disease virus (IBDV), the causative agent of a highly contagious disease in chickens, carries a small nonstructural protein (NS). This protein has been implicated to play a role in the induction of apoptosis. In this study, we investigate the kinetics of viral replication during a single round of viral replication and examine the mechanism of IBDV-induced apoptosis. Our results show that it is caspase dependent and activates caspases 3 and 9. Nuclear factor kappa B (NF-κB) is also activated and is required for IBDV-induced apoptosis. The NF-κB inhibitor MG132 completely inhibited IBDV-induced DNA fragmentation, caspase 3 activation, and NF-κB activation. To study the function of the NS protein in this context, we generated the recombinant rGLS virus and an NS knockout mutant, rGLSNSΔ virus, using reverse genetics. Comparisons of the replication kinetics and markers for virally induced apoptosis indicated that the NS knockout mutant virus induces earlier and increased DNA fragmentation, caspase activity, and NF-κB activation. These results suggest that the NS protein has an antiapoptotic function at the early stage of virus infection.
机译:鸡传染性法氏囊病病毒(IBDV)是一种高度传染性疾病的病原体,携带一种小的非结构蛋白(NS)。已经暗示该蛋白在诱导细胞凋亡中起作用。在这项研究中,我们调查了单轮病毒复制过程中病毒复制的动力学,并研究了IBDV诱导的细胞凋亡的机制。我们的结果表明,它是caspase依赖性的,可以激活caspase 3和9。核因子kappa B(NF-κB)也被激活,是IBDV诱导的细胞凋亡所必需的。 NF-κB抑制剂MG132完全抑制IBDV诱导的DNA片段化,caspase 3激活和NF-κB激活。为了研究NS蛋白在这种情况下的功能,我们使用反向遗传学产生了重组rGLS病毒和NS基因敲除突变体rGLSNSΔ病毒。复制动力学和病毒诱导的凋亡标记的比较表明,NS基因敲除突变体病毒可诱导DNA片段化,胱天蛋白酶活性和NF-κB活化更早和增加。这些结果表明NS蛋白在病毒感染的早期具有抗凋亡功能。

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