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Comparative inhibition of influenza and parainfluenza virus replication by ribavirin in MDCK cells.

机译:利巴韦林在MDCK细胞中比较抑制流感和副流感病毒复制。

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摘要

Actinomycin D inhibited the yield of influenza virus hemagglutinin from MDCK cells infected at high multiplicity, but had little effect on the yield of parainfluenza virus hemagglutinin. In similar hemagglutinin yield experiments, ribavirin was only slightly more active (threefold) against influenza virus than against parainfluenza virus replication. In plaque inhibition experiments, ribavirin depressed influenza virus plaque formation by 50% at a concentration of approximately 3 micrograms/ml, whereas the corresponding figure for parainfluenza viruses was threefold higher. The concentration of ribavirin demonstrating anti-influenza activity was indistinguishable for that inhibiting host cell growth. It is concluded that, unlike actinomycin D, ribavirin is unlikely to have a major effect on the provision of host cell 5-germinal methylated cap structures and the subsequent priming of influenza messenger ribonucleic acid synthesis.
机译:放线菌素D抑制高复数感染的MDCK细胞中流感病毒血凝素的产量,但对副流感病毒血凝素的产量影响很小。在类似的血凝素产量实验中,利巴韦林对流感病毒的活性(对副流感病毒复制的活性)仅稍高(三倍)。在噬菌斑抑制实验中,利巴韦林在大约3微克/毫升的浓度下抑制了50%的流感病毒噬菌斑形成,而副流感病毒的相应数字则高三倍。证明抗流感活性的利巴韦林浓度与抑制宿主细胞生长的浓度没有区别。结论是,与放线菌素D不同,利巴韦林不太可能对宿主细胞5的甲基化甲基化帽结构的提供和随后引发流感信使核糖核酸的合成产生重大影响。

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