Hunt J M, Marcus P I
J Virol. 1974 Jul;14(1):99-109. doi: 10.1128/JVI.14.1.99-109.1974.
Heterologous viral interference is induced by Sindbis virus against vesicular stomatitis virus (VSV) in a manner analogous to intrinsic interference with Newcastle disease virus replication. Interference in both systems (i) depends upon early expression of the inducing virus genome, (ii) shows similar kinetics of induction, (iii) does not involve interferon action, and (iv) appears to be manifest as an all-or-none effect. VSV can be added to the list of viruses blocked by intrinsic interference. Sindbis virus-induced intrinsic interference with VSV replication is not mediated through homotypic interference by defective interfering particles; rather, T-particle and B-particle synthesis is inhibited. Significantly, intrinsic interference has no effect on primary transcription directed by the virion-associated transcriptase in VSV-challenged cells. However, Sindbis virus appears to induce interference with the VSV-RNA synthesized subsequent to primary transcription, namely, that which is dependent on protein synthesis. Thus, the target of intrinsic interference appears to be a reaction subsequent to primary transcription but prior to the appearance of protein synthesis-dependent VSV RNA, secondary transcription.
辛德毕斯病毒对水疱性口炎病毒(VSV)诱导的异源病毒干扰,其方式类似于对新城疫病毒复制的内在干扰。在这两种系统中,干扰(i)取决于诱导病毒基因组的早期表达,(ii)表现出相似的诱导动力学,(iii)不涉及干扰素作用,并且(iv)似乎表现为全或无效应。VSV可被添加到受内在干扰阻断的病毒列表中。辛德毕斯病毒诱导的对VSV复制的内在干扰不是通过缺陷干扰颗粒的同型干扰介导的;相反,T颗粒和B颗粒的合成受到抑制。值得注意的是,内在干扰对VSV感染细胞中由病毒体相关转录酶指导的初级转录没有影响。然而,辛德毕斯病毒似乎对初级转录后合成的VSV-RNA诱导干扰,即依赖于蛋白质合成的那些。因此,内在干扰的靶标似乎是初级转录后但在蛋白质合成依赖性VSV RNA(二级转录)出现之前的反应。