1. Academic Validation
  2. Andrographolide Prevents EV-D68 Replication by Inhibiting the Acidification of Virus-Containing Endocytic Vesicles

Andrographolide Prevents EV-D68 Replication by Inhibiting the Acidification of Virus-Containing Endocytic Vesicles

  • Front Microbiol. 2018 Oct 8;9:2407. doi: 10.3389/fmicb.2018.02407.
Dongyin Wang 1 2 Haoran Guo 2 Junliang Chang 2 3 Dong Wang 1 2 Bin Liu 4 Pujun Gao 1 Wei Wei 2
Affiliations

Affiliations

  • 1 Department of Hepatology, The First Hospital of Jilin University, Jilin University, Changchun, China.
  • 2 Institute of Virology and AIDS Research, The First Hospital of Jilin University, Changchun, China.
  • 3 Changchun Institute of Biological Products, Changchun, China.
  • 4 Department of Hand Surgery, The First Hospital of Jilin University, Changchun, China.
Abstract

Enterovirus D68 (EV-D68) has emerged as a significant respiratory pathogen that can cause severe respiratory disease and acute neurologic disease. At present, there are no approved Antiviral agents or vaccines for EV-D68. In this study, we demonstrate that andrographolide (ADO), an active component of Andrographis paniculata, exerts substantial Antiviral activity against EV-D68 Infection. ADO treatment dramatically inhibited EV-D68 RNA replication (EC50 = 3.45 μM) and protein synthesis without producing significant cytotoxicity at virucidal concentrations. ADO-treated cells did not show any changes in host immune activation, EV-D68 attachment, or viral 5' UTR activity. Using a pH-sensitive fluorescent indicator system for endocytosis in living cells, we found that ADO prevented the acidification of endocytic vesicles after receptor-mediated endocytosis. Finally, we showed that ADO inhibited the viral replication of circulating isolated EV-D68 strains. In summary, our results demonstrate that ADO suppresses EV-D68 replication by targeting the maturation of virus-containing endosomes of EV-D68. This mechanism represents a promising strategy for drug development.

Keywords

acidification; andrographolide; drug development; endocytosis; enterovirus D68.

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