Castilla Viviana, Larzábal Mariano, Sgalippa Natalia Aguirre, Wachsman Mónica B, Coto Celia E
Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón 2, Piso 4, 1428 Buenos Aires, Argentina.
Antiviral Res. 2005 Nov;68(2):88-95. doi: 10.1016/j.antiviral.2005.07.007. Epub 2005 Sep 7.
The antiviral mode of action of the synthetic brassinosteroid (22S,23S)-3beta-bromo-5alpha,22,23-trihydroxystigmastan-6-one (6b) against Junin virus replication in Vero cells was investigated. Time-related experiments showed that 6b mainly affects an early event of virus growth cycle. Neither adsorption nor internalization of viral particles was the target of the inhibitory action. The analysis of the effect of 6b on viral RNA synthesis demonstrated that the presence of the compound adversely affects virus RNA replication by preventing the synthesis of full length antigenomic RNA. Although 6b was most effective the earlier it was added to the cells after infection with JV, a high level of inhibition of JV yield and fusion activity of newly synthesized viral glycoproteins was still detected when the compound was present during the last hours of infection. Therefore, we cannot rule out an inhibitory action of 6b on later events of JV replicative cycle.
研究了合成油菜素内酯(22S,23S)-3β-溴-5α,22,23-三羟基豆甾烷-6-酮(6b)对朱宁病毒在Vero细胞中复制的抗病毒作用模式。与时间相关的实验表明,6b主要影响病毒生长周期的早期事件。病毒颗粒的吸附和内化均不是抑制作用的靶点。对6b对病毒RNA合成的影响分析表明,该化合物的存在通过阻止全长反基因组RNA的合成而对病毒RNA复制产生不利影响。尽管在感染朱宁病毒后越早向细胞中添加6b越有效,但当该化合物在感染的最后几个小时存在时,仍能检测到对朱宁病毒产量和新合成病毒糖蛋白融合活性的高水平抑制。因此,我们不能排除6b对朱宁病毒复制周期后期事件的抑制作用。