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Gliotoxin:一种脊髓灰质炎病毒RNA合成抑制剂,可阻断病毒RNA聚合酶3Dpol。

Gliotoxin: inhibitor of poliovirus RNA synthesis that blocks the viral RNA polymerase 3Dpol.

作者信息

Rodriguez P L, Carrasco L

机构信息

Centro de Biología Molecular, Universidad Autónoma, Madrid, Spain.

出版信息

J Virol. 1992 Apr;66(4):1971-6. doi: 10.1128/JVI.66.4.1971-1976.1992.

DOI:10.1128/JVI.66.4.1971-1976.1992
PMID:1372367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC288985/
Abstract

The mode of action of gliotoxin against poliovirus has been analyzed in detail. This fungal metabolite inhibits the appearance of poliovirus proteins when present from the beginning of infection but has no effect on viral translation when added at late times. In agreement with previous findings, this toxin potently inhibited the incorporation of [3H]uridine into poliovirus RNA soon after its addition to the culture medium. Analysis of the synthesis of poliovirus plus- or minus-stranded RNA in the presence of gliotoxin suggests that this compound effectively hampered both processes. This result contrasts with the mode of action of other inhibitors of poliovirus RNA synthesis, such as guanidine or flavones, that selectively block plus-stranded RNA synthesis and suggests that the target of gliotoxin differs from the target of guanidine, i.e., poliovirus protein 2C. Indeed, gliotoxin was found to be a potent inhibitor of poliovirus RNA synthesis in cell-free systems, using membranous crude replication complexes, a reaction that is not blocked by guanidine or Ro 09-0179. Moreover, in vitro activity of the purified poliovirus polymerase 3Dpol was efficiently inhibited by gliotoxin. These results indicate that this toxin acts on the poliovirus polymerase 3Dpol, providing the first description of an inhibitor of this viral enzyme.

摘要

已对Gliotoxin抗脊髓灰质炎病毒的作用模式进行了详细分析。这种真菌代谢产物在感染开始时存在时会抑制脊髓灰质炎病毒蛋白的出现,但在后期添加时对病毒翻译没有影响。与先前的研究结果一致,这种毒素在添加到培养基后不久就能有效抑制[3H]尿苷掺入脊髓灰质炎病毒RNA。在Gliotoxin存在的情况下对脊髓灰质炎病毒正链或负链RNA合成的分析表明,这种化合物有效地阻碍了这两个过程。这一结果与脊髓灰质炎病毒RNA合成的其他抑制剂(如胍或黄酮)的作用模式形成对比,后者选择性地阻断正链RNA合成,表明Gliotoxin的作用靶点与胍的作用靶点不同,即脊髓灰质炎病毒蛋白2C。事实上,使用膜性粗复制复合物,发现在无细胞系统中Gliotoxin是脊髓灰质炎病毒RNA合成的有效抑制剂,而胍或Ro 09-0179不会阻断该反应。此外,纯化的脊髓灰质炎病毒聚合酶3Dpol的体外活性被Gliotoxin有效抑制。这些结果表明,这种毒素作用于脊髓灰质炎病毒聚合酶3Dpol,首次描述了这种病毒酶的一种抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/794cdd2870be/jvirol00166-0160-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/82b646e3b228/jvirol00166-0158-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/3b1492e8395c/jvirol00166-0159-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/794cdd2870be/jvirol00166-0160-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/82b646e3b228/jvirol00166-0158-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/3b1492e8395c/jvirol00166-0159-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d4/288985/794cdd2870be/jvirol00166-0160-a.jpg

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