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三萜类化合物苦瓜素-Ic通过阻止真核细胞中基因表达的起始来抑制人巨细胞病毒。

The Triterpenoid MOMORDIN-Ic Inhibits HCMV by Preventing the Initiation of Gene Expression in Eukaryotic Cells.

作者信息

Bradley Eleanor, Poole Emma, Reeves Matthew B

机构信息

Institute of Immunity & Transplantation, Division of Infection & Immunity, UCL, Royal Free Campus, London NW3 2PP, UK.

Division of Virology, Department of Pathology, University of Cambridge, Addenbrooke's Campus, Cambridge CB2 0QQ, UK.

出版信息

Pathogens. 2024 Jun 28;13(7):546. doi: 10.3390/pathogens13070546.

Abstract

Human cytomegalovirus (HCMV) primary infection, re-infection, and reactivation from latency cause morbidity in immune-compromised patients. Consequently, potential therapeutic strategies remain of interest for the treatment of infection. Naturally occurring triterpenoids derived from plants have been demonstrated to have anti-viral activity, although their precise mechanisms of action are not always fully understood. Here, we investigate the activity of Mormordin Ic (Mc) and demonstrate that it is potently anti-viral against HCMV. Through investigation of the mechanistic basis of this anti-viral activity, we identify that it is inhibitory to both viral and host gene expression, and to highly induced genes in particular. We go on to observe that Mc impacts on RNA Pol II activity and, specifically, reduces the occupancy of elongating RNA Pol II at a viral promoter. Next, we demonstrate that Mc is inhibitory to HCMV reactivation, and in doing so identify that it has greater activity against the canonical major immediate early promoter compared to the alternative ip2 promoter located downstream. Finally, we see evidence of RNA Pol II occupancy at the ip2 promoter in undifferentiated myeloid cells. Thus, Mc is potently anti-viral and a potential tool to probe the activity of multiple promoters considered important for controlling HCMV reactivation.

摘要

人巨细胞病毒(HCMV)的原发性感染、再感染以及潜伏状态的重新激活会导致免疫功能低下患者发病。因此,潜在的治疗策略仍是治疗该感染的研究热点。植物来源的天然三萜类化合物已被证明具有抗病毒活性,尽管其确切作用机制并不总是完全清楚。在此,我们研究了莫莫汀Ic(Mc)的活性,并证明它对HCMV具有强效抗病毒作用。通过研究这种抗病毒活性的机制基础,我们发现它对病毒和宿主基因表达均有抑制作用,尤其对高度诱导的基因。我们进一步观察到Mc影响RNA聚合酶II(RNA Pol II)的活性,具体而言,它会降低延伸中的RNA Pol II在病毒启动子上的占有率。接下来,我们证明Mc对HCMV的重新激活具有抑制作用,并在此过程中发现,与位于下游的替代ip2启动子相比,它对典型的主要立即早期启动子具有更强的活性。最后,我们在未分化的髓样细胞中观察到RNA Pol II在ip2启动子上占有率的证据。因此,Mc具有强效抗病毒作用,是一种潜在工具,可用于探究对控制HCMV重新激活至关重要的多个启动子的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8926/11280373/09ce9dc783ed/pathogens-13-00546-g001.jpg

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