Díaz-Guerra M, Kahn J S, Esteban M
Department of Biochemistry, State University of New York, Brooklyn 11203.
Virology. 1993 Nov;197(1):485-91. doi: 10.1006/viro.1993.1618.
The role of vaccinia virus nucleoside triphosphate phosphohydrolase I (NPH-I) in determining the resistance of this virus to alpha-interferon (IFN) was analyzed by using a well-defined temperature-sensitive mutant (ts36) in the NPH-I gene. Detailed analysis of viral proteins and mRNAs produced in cultured cells treated with or without IFN-alpha showed a strong inhibition by IFN of the synthesis of late virus polypeptides at the nonpermissive temperature, e.g., 83.8% inhibition for the luciferase reporter gene, which is associated with a decrease in steady-state mRNA levels. Sensitivity of ts36 to IFN was only the consequence of the point mutation in the NPH-1 gene, as shown by characterization of the rescued virus, R36. Our findings demonstrate that functional NPH-1 is required, at least in part, for resistance of vaccinia virus to IFN.
通过使用NPH-I基因中一个明确的温度敏感突变体(ts36),分析了痘苗病毒核苷三磷酸磷酸水解酶I(NPH-I)在决定该病毒对α干扰素(IFN)抗性中的作用。对用或不用IFN-α处理的培养细胞中产生的病毒蛋白和mRNA的详细分析表明,在非允许温度下,IFN对晚期病毒多肽的合成有强烈抑制作用,例如,对荧光素酶报告基因的抑制率为83.8%,这与稳态mRNA水平的降低有关。如拯救病毒R36的特性所示,ts36对IFN的敏感性仅是NPH-1基因中该点突变的结果。我们的研究结果表明,功能性NPH-1至少部分是痘苗病毒对IFN产生抗性所必需的。