Grimley P M, Moss B
J Virol. 1971 Aug;8(2):225-31. doi: 10.1128/JVI.8.2.225-231.1971.
Membrane-limited structures, resembling virus envelope precursors previously shown to form during the interruption of poxvirus assembly by rifampin, were now observed by electron microscopy in vaccinia-infected HeLa cells treated with a series of rifamycin derivatives. The active compounds N-demethyl rifampin, AF/DMI, and 3-formyl rifamycin SV lacked, respectively, a methyl group, the piperazine ring, and the hydrazone portion of rifampin. A vaccinia mutant selected only for resistance to rifampin was also resistant to the effect on morphogenesis produced by all of the rifamycin derivatives. We concluded that this antiviral effect was specific and was a property associated with the macrocyclic ring rather than the hydrazone-containing side chain of rifampin. In addition to their effects on vaccinia morphogenesis, 3-formyl rifamycin SV and AF/DMI had unusual cytotoxic effects.
通过电子显微镜观察发现,在用一系列利福霉素衍生物处理的感染痘苗病毒的HeLa细胞中,出现了膜性受限结构,其类似于先前在利福平中断痘苗病毒装配过程中形成的病毒包膜前体。活性化合物N-去甲基利福平、AF/DMI和3-甲酰基利福霉素SV分别缺少利福平的一个甲基、哌嗪环和腙部分。仅选择对利福平具有抗性的痘苗病毒突变体对所有利福霉素衍生物对形态发生的影响也具有抗性。我们得出结论,这种抗病毒作用是特异性的,并且是与大环而非利福平含腙侧链相关的特性。除了对痘苗病毒形态发生的影响外,3-甲酰基利福霉素SV和AF/DMI还具有不同寻常的细胞毒性作用。