Alarcon B, Bugany H, Carrasco L
J Virol. 1984 Oct;52(1):183-7. doi: 10.1128/JVI.52.1.183-187.1984.
pppA2'p5'A blocked the production of infectious vesicular stomatitis virus in HeLa cells. When this compound was present from the beginning of infection, a selective inhibitory effect was observed in viral protein synthesis. Thus, cellular translation was not affected even after 10 h of incubation with this compound, and the bulk of viral proteins was not synthesized. However, this effect was not observed with ATP, GTP, or the core A2'p5'A. The step blocked by pppA2'p5'A is located early during virus infection, but adsorption, entry, and virus uncoating seemed to be unaffected by this compound. Analysis of the antiviral spectrum of pppA2'p5'A indicated that it is active against poliovirus, encephalomyocarditis virus, and Semliki Forest virus and shows no effect against herpes simplex virus type 1 and adenovirus type 5.
pppA2'p5'A可阻断HeLa细胞中传染性水疱性口炎病毒的产生。当从感染开始就存在这种化合物时,在病毒蛋白质合成中观察到选择性抑制作用。因此,即使与该化合物孵育10小时后,细胞翻译也未受影响,且大部分病毒蛋白质未合成。然而,ATP、GTP或核心A2'p5'A未观察到这种作用。pppA2'p5'A阻断的步骤位于病毒感染早期,但吸附、进入和病毒脱壳似乎不受该化合物影响。对pppA2'p5'A抗病毒谱的分析表明,它对脊髓灰质炎病毒、脑心肌炎病毒和Semliki森林病毒有活性,而对1型单纯疱疹病毒和5型腺病毒无作用。