Natural Products and Derivatives as Potential Zika virus Inhibitors: A Comprehensive Review

Viruses. 2023 May 20;15(5):1211. doi: 10.3390/v15051211.

Abstract

Zika virus (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 = CC50/EC50), were reported for epigallocatechin gallate (SI ≥ 25,000) and anisomycin (SI ≥ 11,900) obtained from Streptomyces bacteria, dolastane (SI = 1246) isolated from the marine seaweed Canistrocarpus cervicorni, 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.

Keywords: anti-ZIKV compounds; in silico assays; in vitro assays; in vivo assays; natural products.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • Biological Products* / pharmacology
  • Biological Products* / therapeutic use
  • Chlorocebus aethiops
  • Humans
  • Vero Cells
  • Virus Replication
  • Zika Virus Infection*
  • Zika Virus*

Substances

  • Biological Products
  • Antiviral Agents

Grants and funding

This study received support from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil (grant 421563/2018-4 to F.C.B.), as well as from the INCT-CNPq Program (grant 465425/2014-3 to M.M.T.).