Andrographolide and Its 14-Aryloxy Analogues Inhibit Zika and Dengue Virus Infection

Molecules. 2020 Oct 30;25(21):5037. doi: 10.3390/molecules25215037.

Abstract

Andrographolide is a labdene diterpenoid with potential applications against a number of viruses, including the mosquito-transmitted dengue virus (DENV). In this study, we evaluated the anti-viral activity of three 14-aryloxy analogues (ZAD-1 to ZAD-3) of andrographolide against Zika virus (ZIKV) and DENV. Interestingly, one analogue, ZAD-1, showed better activity against both ZIKV and DENV than the parental andrographolide. A two-dimension (2D) proteomic analysis of human A549 cells treated with ZAD-1 compared to cells treated with andrographolide identified four differentially expressed proteins (heat shock 70 kDa protein 1 (HSPA1A), phosphoglycerate kinase 1 (PGK1), transketolase (TKT) and GTP-binding nuclear protein Ran (Ran)). Western blot analysis confirmed that ZAD-1 treatment downregulated expression of HSPA1A and upregulated expression of PGK1 as compared to andrographolide treatment. These results suggest that 14-aryloxy analogues of andrographolide have the potential for further development as anti-DENV and anti-ZIKV agents.

Keywords: HSPA1A; PGK1; Zika virus; andrographolide; dengue virus.

MeSH terms

  • A549 Cells
  • Antiviral Agents* / chemistry
  • Antiviral Agents* / pharmacology
  • Dengue / drug therapy*
  • Dengue / metabolism
  • Dengue / pathology
  • Dengue Virus / growth & development*
  • Diterpenes* / chemistry
  • Diterpenes* / pharmacology
  • HEK293 Cells
  • Humans
  • Zika Virus / growth & development*
  • Zika Virus Infection / drug therapy*
  • Zika Virus Infection / metabolism
  • Zika Virus Infection / pathology

Substances

  • Antiviral Agents
  • Diterpenes
  • andrographolide