Direkt zum Inhalt
Direkt zum Inhalt

Neue Veröffentlichung in Scientific Reports: Domperidone inhibits dengue virus infection by targeting the viral envelope protein and nonstructural protein 1

Veröffentlichung von der Arbeitsgruppe Theoretische Chemie in Zusammenarbeit mit der Arbeitsgruppe von Sansanee Noisakran erschienen in Scientific Reports im Jahr 2025

Abstrakt

Dengue is a mosquito-borne disease caused by dengue virus (DENV) infection, which remains a major
public health concern worldwide owing to the lack of specific treatments or antiviral drugs available.
This study investigated the potential repurposing of domperidone, an antiemetic and gastrokinetic
agent, to control DENV infection. Domperidone was identified by pharmacophore-based virtual
screening as a small molecule that can bind to both the viral envelope (E) and the nonstructural protein
1 (NS1) of DENV. Molecular dynamics (MD) simulations and surface plasmon resonance (SPR) analysis
were subsequently performed to determine specific interactions of domperidone with the DENV E and
NS1 proteins and their binding affinity. Treatment of immortalized human hepatocyte-like cells (imHC)
with domperidone could inhibit DENV production and NS1 secretion in a dose-dependent manner
following infection with DENV serotype 2. These inhibitory effects were mediated by reduction in viral
RNA replication and viral E and NS1 protein expression, but not by interference with virus entry into
cells or NS1 oligomerization. The suppression of DENV production and NS1 secretion by domperidone
was observed across all four DENV serotypes to varying degrees between different virus strains. The
findings from our study suggest viral target-based repurposing of domperidone for modulating DENV.

 

Referenz

Kaewjiw N, Thaingtamtanha T, Mehra D, Chawnawa W, Prommool T, Puttikhunt C, Songjaeng A, Kongmanas K, Avirutnan P, Luangaram P, Srisawat C, Roytrakul S, Bäurle SA, Noisakran S. Domperidone inhibits dengue virus infection by targeting the viral envelope protein and nonstructural protein 1. Sci Rep. 2025 Jan 30;15(1):3817. doi: 10.1038/s41598-025-87146-w

 

Ansprechpartner

Stephan Bäurle Universität Siegen

PD Dr. Stephan Bäurle

Mitglied des ZiGS
Icon Nachricht

Kontakt Pressestelle

Stabsstelle für Presse, Kommunikation und Marketing

  • Icon Mail

    presse@uni-siegen.de

  • Icon Kartennadel

    Adolf-Reichwein-Straße 2a

    Gebäude AVZ (Gebäudeteil AR-NA)

    57068 Siegen

Universität Siegen Adolf-Reichwein-Campus