Marques M I, Costa J V
Gulbenkian Institute of Science, Oeiras, Portugal.
Virology. 1992 Nov;191(1):498-501. doi: 10.1016/0042-6822(92)90219-f.
African swine fever virus (ASFV) induces the synthesis of a virus-specific DNA polymerase, which is inhibited by phosphonoacetic acid and cytosine arabinoside. In contrast to all other alpha-like DNA polymerases of DNA viruses, ASFV-specific DNA polymerase is resistant to aphidicolin. Concentrations of the drug as high as 160 microM had no effect on virus production or plaquing efficiency. The resistance of ASFV DNA polymerase to aphidicolin was confirmed by analyzing the effect of the drug on viral DNA synthesis. A moderate inhibition of viral DNA synthesis was observed when aphidicolin was added immediately after virus adsorption but normal synthesis occurred, with a peak at 10 hr p.i., when the drug was added at 2 or 4 hr p.i. This suggests that a very early phase of ASFV DNA replication is sensitive to aphidicolin and is probably catalyzed by a different enzyme. An in vitro assay of DNA polymerase activity was used to assay the sensitivity of the virus-specific DNA polymerase to inhibitors. In correspondence to the results observed in vivo, phosphonoacetic acid strongly inhibited the enzyme activity, whereas aphidicolin had no effect. Resistance to aphidicolin was independent of the concentration of dCTP used in the assay. Three independent ASFV mutants resistant to phosphonoacetic acid showed the same resistance to aphidicolin as wild type virus.
非洲猪瘟病毒(ASFV)可诱导一种病毒特异性DNA聚合酶的合成,该酶受到膦甲酸和阿糖胞苷的抑制。与DNA病毒的所有其他α样DNA聚合酶不同,ASFV特异性DNA聚合酶对阿非迪霉素具有抗性。高达160 microM的药物浓度对病毒产生或噬斑形成效率没有影响。通过分析该药物对病毒DNA合成的影响,证实了ASFV DNA聚合酶对阿非迪霉素的抗性。当在病毒吸附后立即添加阿非迪霉素时,观察到病毒DNA合成受到适度抑制,但当在感染后2或4小时添加该药物时,正常合成发生,在感染后10小时达到峰值。这表明ASFV DNA复制的一个非常早期阶段对阿非迪霉素敏感,可能由一种不同的酶催化。使用DNA聚合酶活性的体外测定法来测定病毒特异性DNA聚合酶对抑制剂的敏感性。与体内观察到的结果一致,膦甲酸强烈抑制酶活性,而阿非迪霉素没有影响。对阿非迪霉素的抗性与测定中使用的dCTP浓度无关。三个独立的对膦甲酸具有抗性的ASFV突变体对阿非迪霉素的抗性与野生型病毒相同。