In Vitro Antiviral Activity of α-Mangostin against Dengue Virus Serotype-2 (DENV-2).
FFU assay
IFA
antiviral
dengue
quantitative RT-PCR
xanthonoids
α-Mangostin
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
19 May 2021
19 May 2021
Historique:
received:
15
03
2021
revised:
29
04
2021
accepted:
05
05
2021
entrez:
2
6
2021
pubmed:
3
6
2021
medline:
27
7
2021
Statut:
epublish
Résumé
Dengue virus (DENV), a member of the family Flaviviridae, is a threat for global health as it infects more than 100 million people yearly. Approved antiviral therapies or vaccines for the treatment or prevention of DENV infections are not available. In the present study, natural compounds were screened for their antiviral activity against DENV by in vitro cell line-based assay. α-Mangostin, a xanthanoid, was observed to exert antiviral activity against DENV-2 under pre-, co- and post-treatment testing conditions. The antiviral activity was determined by foci forming unit (FFU) assay, quantitative RT-PCR and cell-based immunofluorescence assay (IFA). A complete inhibition of DENV-2 was observed at 8 µM under the co-treatment condition. The possible inhibitory mechanism of α-Mangostin was also determined by docking studies. The molecular docking experiments indicate that α-Mangostin can interact with multiple DENV protein targets such as the NS5 methyltransferase, NS2B-NS3 protease and the glycoprotein E. The in vitro and in silico findings suggest that α-Mangostin possesses the ability to suppress DENV-2 production at different stages of its replication cycle and might act as a prophylactic/therapeutic agent against DENV-2.
Identifiants
pubmed: 34069351
pii: molecules26103016
doi: 10.3390/molecules26103016
pmc: PMC8158742
pii:
doi:
Substances chimiques
Antiviral Agents
0
Xanthones
0
mangostin
U6RIV93RU1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Indian Council of Medical Research
ID : VIR/32/2019/ECD-I
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