Department of Pharmaceutical Products, Faculty of Pharmacy, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, MG, Brazil.
Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, MG, Brazil.
Viruses. 2023 May 20;15(5):1211. doi: 10.3390/v15051211.
(ZIKV) is an arbovirus whose infection in humans can lead to severe outcomes. This article reviews studies reporting the anti-ZIKV activity of natural products (NPs) and derivatives published from 1997 to 2022, which were carried out with NPs obtained from plants (82.4%) or semisynthetic/synthetic derivatives, fungi (3.1%), bacteria (7.6%), animals (1.2%) and marine organisms (1.9%) along with miscellaneous compounds (3.8%). Classes of NPs reported to present anti-ZIKV activity include polyphenols, triterpenes, alkaloids, and steroids, among others. The highest values of the selectivity index, the ratio between cytotoxicity and antiviral activity (SI = CC/EC), were reported for epigallocatechin gallate (SI ≥ 25,000) and anisomycin (SI ≥ 11,900) obtained from bacteria, dolastane (SI = 1246) isolated from the marine seaweed , and the flavonol myricetin (SI ≥ 862). NPs mostly act at the stages of viral adsorption and internalization in addition to presenting virucidal effect. The data demonstrate the potential of NPs for developing new anti-ZIKV agents and highlight the lack of studies addressing their molecular mechanisms of action and pre-clinical studies of efficacy and safety in animal models. To the best of our knowledge, none of the active compounds has been submitted to clinical studies.
(ZIKV)是一种虫媒病毒,其感染人类可导致严重后果。本文综述了 1997 年至 2022 年期间发表的关于天然产物(NPs)及其衍生物抗 ZIKV 活性的研究报告,这些研究使用了来自植物(82.4%)或半合成/合成衍生物、真菌(3.1%)、细菌(7.6%)、动物(1.2%)和海洋生物(1.9%)以及杂类化合物(3.8%)的 NPs。报告具有抗 ZIKV 活性的 NPs 类别包括多酚、三萜、生物碱和类固醇等。报道的最高细胞毒性指数选择性指数(SI = CC/EC)值分别为来源于细菌的表没食子儿茶素没食子酸酯(SI ≥ 25,000)和anisomycin(SI ≥ 11,900)、从海洋海藻中分离得到的 dolastane(SI = 1246)以及黄酮醇杨梅素(SI ≥ 862)。NPs 主要作用于病毒吸附和内化阶段,此外还具有杀病毒作用。这些数据表明 NPs 具有开发新型抗 ZIKV 药物的潜力,并强调了缺乏针对其作用机制和在动物模型中进行疗效和安全性的临床前研究的情况。据我们所知,没有一种活性化合物已经提交给临床研究。