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米替福新抑制基孔肯雅病毒在人原代表皮成纤维细胞中的复制。

Miltefosine inhibits Chikungunya virus replication in human primary dermal fibroblasts.

作者信息

Sharma Anuj, Bhomia Manish, Yeh Tze-Jou, Singh Jay, Maheshwari Radha K

机构信息

Department of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA.

出版信息

F1000Res. 2018 Jan 4;7:9. doi: 10.12688/f1000research.13242.1. eCollection 2018.

Abstract

: Chikungunya virus (CHIKV) is a re-emerging pathogen that has caused widespread outbreaks affecting millions of people around the globe. Currently, there is no specific therapeutic drug against CHIKV, with symptomatic treatment only to manage the disease. Pi3-akt signaling has been implicated in infection of several viruses including that of CHIKV. Effect of Pi3-akt signaling inhibitors on CHIKV replication was evaluated in this study. : Human primary dermal fibroblast cells were treated with inhibitors of the Pi3-akt signaling pathway. Suppression of CHIKV replication was evaluated as reduction in virus titer in cell supernatants. Effect of miltefosine (MF) on CHIKV replication was evaluated in pre and post treatment regimen. Inhibition of virus replication was determined by cell growth, virus titer and western blot. : Inhibition of Akt-phosphorylation significantly inhibited CHIKV replication. No effect on CHIKV replication was observed after treatment with Pi3-kinase and mTOR activation inhibitors. Further, MF, an FDA-approved Akt-inhibitor, inhibited CHIKV replication in pre- and post-infection treatment regimens. : Data suggests that Akt-phosphorylation can be an amenable target of therapy against CHIKV infection. This is the first study to show inhibition of CHIKV replication by MF, and presents a case for further development of MF as an anti-CHIKV drug.

摘要

基孔肯雅病毒(CHIKV)是一种再度出现的病原体,已引发广泛疫情,影响全球数百万人。目前,尚无针对CHIKV的特效治疗药物,仅采用对症治疗来控制病情。PI3-AKT信号通路与包括CHIKV在内的多种病毒感染有关。本研究评估了PI3-AKT信号通路抑制剂对CHIKV复制的影响。:用人原代表皮成纤维细胞用PI3-AKT信号通路抑制剂进行处理。通过细胞上清液中病毒滴度的降低来评估对CHIKV复制的抑制作用。在治疗前和治疗后方案中评估米替福新(MF)对CHIKV复制的影响。通过细胞生长、病毒滴度和蛋白质印迹法来确定病毒复制的抑制情况。:抑制Akt磷酸化可显著抑制CHIKV复制。用PI3激酶和mTOR激活抑制剂处理后,未观察到对CHIKV复制有影响。此外,MF是一种经美国食品药品监督管理局批准的Akt抑制剂,在感染前和感染后治疗方案中均能抑制CHIKV复制。:数据表明,Akt磷酸化可能是针对CHIKV感染的一个合适治疗靶点。这是第一项显示MF可抑制CHIKV复制的研究,并为进一步开发MF作为抗CHIKV药物提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01e7/5795271/3f17d1da7459/f1000research-7-14366-g0000.jpg

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