Iqbal Munir, Poole Emma, Goodbourn Stephen, McCauley John W
Institute for Animal Health, Compton Laboratory, Compton, Newbury, Berkshire RG20 7NN, United Kingdom.
J Virol. 2004 Jan;78(1):136-45. doi: 10.1128/jvi.78.1.136-145.2004.
Production of alpha/beta interferon in response to viral double-stranded RNA (dsRNA) produced during viral replication is a first line of defense against viral infections. Here we demonstrate that the Erns glycoprotein of the pestivirus bovine viral diarrhea virus can act as an inhibitor of dsRNA-induced responses of cells. This effect is seen whether Erns is constitutively expressed in cells or exogenously added to the culture medium. The Erns effect is specific to dsRNA since activation of NF-kappaB in cells infected with Semliki Forest virus or treated with tumor necrosis factor alpha was not affected. We also show that Erns contains a dsRNA-binding activity, and its RNase is active against dsRNA at a low pH. Both the dsRNA binding and RNase activities are required for the inhibition of dsRNA signaling, and we discuss here a model to account for these observations.
在病毒复制过程中产生的病毒双链RNA(dsRNA)引发的α/β干扰素的产生是抵御病毒感染的第一道防线。在此我们证明,瘟病毒牛病毒性腹泻病毒的Erns糖蛋白可作为细胞dsRNA诱导反应的抑制剂。无论Erns是在细胞中组成性表达还是外源添加到培养基中,均可观察到这种效应。Erns的效应是dsRNA特异性的,因为感染辛德毕斯病毒或用肿瘤坏死因子α处理的细胞中NF-κB的激活不受影响。我们还表明,Erns具有dsRNA结合活性,并且其RNase在低pH下对dsRNA具有活性。dsRNA结合和RNase活性都是抑制dsRNA信号传导所必需的,我们在此讨论一个解释这些观察结果的模型。