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脑心肌炎病毒前导序列参与宿主细胞蛋白质合成的抑制。

Mengovirus leader is involved in the inhibition of host cell protein synthesis.

作者信息

Zoll J, Galama J M, van Kuppeveld F J, Melchers W J

机构信息

Department of Medical Microbiology, University of Nijmegen, The Netherlands.

出版信息

J Virol. 1996 Aug;70(8):4948-52. doi: 10.1128/JVI.70.8.4948-4952.1996.

Abstract

The presence of a leader peptide in picornaviruses is restricted to the Cardiovirus and Aphthovirus genera. However, the leader peptides of these two genera are structurally and functionally unrelated. The aphthovirus leader is a protease involved in viral polyprotein processing and host cell translation shutoff. The function of the cardiovirus leader peptide is still unknown. To gain an insight into the function of the cardiovirus leader peptide, a mengovirus leader peptide deletion mutant was constructed. The deletion mutant was able to grow at a reduced rate in baby hamster kidney cells (BHK-21). Mutant virus production in mouse fibroblasts (L929 cells), however, could be demonstrated only after inoculation of BHK-21 cells with the transfected L929 cells. Analysis of cellular and viral protein synthesis in mutant virus-infected cells showed a delayed inhibition of host cell protein synthesis and a reduced production of viral proteins. In a single-cycle infection, mutant virus produced only 1% of wild-type virus yield at 8 h postinfection. Host cell translation shutoff in L929 cells infected with mutant virus was restored by the addition of the kinase inhibitor 2-aminopurine. Mutant virus production in 2-aminopurine-treated L929 cells was increased to 60% of wild-type virus yield at 8 h postinfection. Our results suggest that the cardiovirus leader peptide is involved in the inhibition of host cell protein synthesis.

摘要

微小核糖核酸病毒中的前导肽仅存在于心病毒属和口蹄疫病毒属中。然而,这两个属的前导肽在结构和功能上并无关联。口蹄疫病毒前导肽是一种参与病毒多聚蛋白加工和宿主细胞翻译关闭的蛋白酶。心病毒前导肽的功能仍然未知。为了深入了解心病毒前导肽的功能,构建了一种脑心肌炎病毒前导肽缺失突变体。该缺失突变体能够在幼仓鼠肾细胞(BHK - 21)中以较低的速率生长。然而,只有在用转染的L929细胞接种BHK - 21细胞后,才能在小鼠成纤维细胞(L929细胞)中检测到突变病毒的产生。对突变病毒感染细胞中的细胞和病毒蛋白合成分析表明,宿主细胞蛋白合成的抑制延迟,且病毒蛋白产量降低。在单循环感染中,突变病毒在感染后8小时产生的病毒产量仅为野生型病毒产量的1%。通过添加激酶抑制剂2 - 氨基嘌呤,可恢复感染突变病毒的L929细胞中的宿主细胞翻译关闭。在感染后8小时,用2 - 氨基嘌呤处理的L929细胞中突变病毒的产量增加到野生型病毒产量的60%。我们的结果表明,心病毒前导肽参与抑制宿主细胞蛋白合成。

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