Insight into the Natural Biomolecules (BMs): Promising Candidates as Zika Virus Inhibitors.

Kiran Dobhal, Ruchika Garg, Alka Singh, Amit Semwal
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Abstract

Zika virus (ZIKV) is among the relatively new infectious disease threats that include SARS-CoV-2, coronavirus, monkeypox (Mpox) virus, etc. ZIKV has been reported to cause severe health risks to the fetus. To date, satisfactory treatment is still not available for the treatment of ZIKV infection. This review examines the last five years of work using natural biomolecules (BMs) to counteract the ZIKV through virtual screening and in vitro investigations. Virtual screening has identified doramectin, pinocembrin, hesperidins, epigallocatechin gallate, pedalitin, and quercetin as potentially active versus ZIKV infection. In vitro, testing has shown that nordihydroguaiaretic acid, mefloquine, isoquercitrin, glycyrrhetinic acid, patentiflorin-A, rottlerin, and harringtonine can reduce ZIKV infections in cell lines. However, in vivo, testing is limited, fortunately, emetine, rottlerin, patentiflorin-A, and lycorine have shown in vivo anti- ZIKV potential. This review focuses on natural biomolecules that show a particularly high selective index (>10). There is limited in vivo and clinical trial data for natural BMs, which needs to be an active area of investigation. This review aims to compile the known reference data and discuss the barriers associated with discovering and using natural BM agents to control ZIKV infection.

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洞察天然生物分子(BMs):有望成为寨卡病毒抑制剂的候选物质。
寨卡病毒(ZIKV)是与 SARS-CoV2、冠状病毒、猴痘(Mpox)病毒等并列的相对较新的传染病威胁之一。据报道,寨卡病毒会对胎儿的健康造成严重危害。迄今为止,治疗 ZIKV 感染的方法仍不尽人意。本综述通过虚拟筛选和体外研究,对过去五年利用天然生物大分子(BMs)对抗 ZIKV 的工作进行了研究。通过虚拟筛选发现,多拉菌素、皮诺虫草素、橙皮甙、表没食子儿茶素没食子酸酯、踏板素和槲皮素对 ZIKV 感染具有潜在的活性。体外测试表明,正氢愈创木脂酸、甲氟喹、异槲皮素、甘草亭酸、漆树苷-A、腐霉利素和哈灵宁可以减少细胞系中的 ZIKV 感染。然而,在体内进行的测试还很有限,幸运的是,依美汀、腐竹素、漆树花素-A 和番荔枝碱已在体内显示出抗 ZIKV 的潜力。本综述主要关注那些显示出特别高选择性指数(大于 10)的天然生物分子。天然生物分子的体内和临床试验数据有限,这需要成为一个积极的研究领域。本综述旨在汇编已知的参考数据,并讨论发现和使用天然生物分子制剂控制 ZIKV 感染的相关障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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