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次生代谢产物作为对抗寨卡病毒的潜在候选药物,寨卡病毒是一种新出现的迫在眉睫的人类威胁:当前形势、分子机制及未来挑战

Secondary metabolites as potential drug candidates against Zika virus, an emerging looming human threat: Current landscape, molecular mechanism and challenges ahead.

作者信息

Sadeer Nabeelah Bibi, El Kalamouni Chaker, Khalid Asaad, Abdalla Ashraf N, Zengin Gokhan, Khoa Bao Le Van, Mahomoodally Mohamad Fawzi

机构信息

Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, Mauritius.

Unité Mixte Processus Infectieux en Milieu Insulaire Tropical, Plateforme Technologique CYROI, Université de la Réunion, INSERM U1187, CNRS UMR 9192, IRD UMR 249, 94791 Sainte Clotilde, La Réunion, France.

出版信息

J Infect Public Health. 2023 May;16(5):754-770. doi: 10.1016/j.jiph.2023.03.008. Epub 2023 Mar 15.

Abstract

Nature has given us yet another wild card in the form of Zika virus (ZIKV). It was found in 1947, but has only recently become an important public health risk, predominantly to pregnant women and their unborn offspring. Currently, no specific therapeutic agent exists for ZIKV and treatment is mainly supportive. Natural products (NPs) can serve as a major source of potent antiviral drugs. To create this review, a comprehensive search was conducted from different databases (PubMed, ScienceDirect, Google scholar). A statistical analysis on the number of publications related to NPs and ZIKV was conducted to analyse the trend in research covering the period 1980-2020. From the data collated in this review, a number of NPs have been found to be inhibitive towards different stages of the ZIKV lifecycle in in vitro studies. For instance, baicalin, (-)-epigallocatechin gallate, curcumin, nanchangmycin, gossypol, cephaeline, emetine, resveratrol, berberine, amongst others, can prevent viral entry by attacking ZIKV E protein. Compounds luteolin, myricetin, astragalin, rutin, (-)-epigallocatechin gallate, carnosine, pedalitin, amongst others, inhibited NS2B-NS3 protease activity which consequently hamper replication. Interestingly, a few NPs had the ability to arrest both viral entry and replication, namely baicalin, (-)-epigallocatechin gallate, curcumin, cephaeline, emetine, and resveratrol. To the best of our knowledge, we obtained only one in vivo study conducted on emetine and results showed that it decreased the levels of circulating ZIKV by approximately 10-fold. Our understanding on NPs exhibiting anti-ZIKV effects in in vivo testing as well as clinical trials is limited. Our trend analysis showed that interest in searching for a cure or prevention against Zika in NPs is negligible and there are no publications yet covering the clinical evaluation. NPs with anti-ZIKV property can a winning strategy in controlling the bio-burden of an epidemic or pandemic. We therefore opine that in the future, more research should be devoted to ZIKV. This review attempts to provide baseline data and roadmap to pursuit detailed investigations for developing potent and novel therapeutic agents to prevent and cure ZIKV infection.

摘要

大自然以寨卡病毒(ZIKV)的形式又给了我们一张“百搭牌”。它于1947年被发现,但直到最近才成为一个重要的公共卫生风险,主要影响孕妇及其未出生的后代。目前,针对寨卡病毒没有特效治疗药物,治疗主要是支持性的。天然产物(NPs)可以成为强效抗病毒药物的主要来源。为撰写本综述,我们从不同数据库(PubMed、ScienceDirect、谷歌学术)进行了全面检索。对与天然产物和寨卡病毒相关的出版物数量进行了统计分析,以分析1980年至2020年期间的研究趋势。根据本综述整理的数据,在体外研究中发现许多天然产物对寨卡病毒生命周期的不同阶段具有抑制作用。例如,黄芩苷、(-)-表没食子儿茶素没食子酸酯、姜黄素、南昌霉素、棉酚、吐根碱、依米丁、白藜芦醇、黄连素等,可以通过攻击寨卡病毒E蛋白来阻止病毒进入。木犀草素、杨梅素、黄芪苷、芦丁、(-)-表没食子儿茶素没食子酸酯、肌肽、pedalitin等化合物抑制NS2B-NS3蛋白酶活性,从而阻碍病毒复制。有趣的是,一些天然产物能够同时阻止病毒进入和复制,即黄芩苷、(-)-表没食子儿茶素没食子酸酯、姜黄素、吐根碱、依米丁和白藜芦醇。据我们所知,我们仅获得了一项针对依米丁的体内研究,结果表明它使循环中的寨卡病毒水平降低了约10倍。我们对天然产物在体内试验以及临床试验中表现出的抗寨卡病毒作用的了解有限。我们的趋势分析表明,在天然产物中寻找寨卡病毒治疗或预防方法的研究兴趣微乎其微,目前还没有关于临床评估的出版物。具有抗寨卡病毒特性的天然产物可能是控制流行病或大流行生物负担的成功策略。因此,我们认为未来应该对寨卡病毒进行更多研究。本综述试图提供基线数据和路线图,以推动开展详细研究,开发有效且新颖的治疗药物来预防和治疗寨卡病毒感染。

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