Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)

Enterovirus A71 (EV-A71) is a major neurovirulent agent capable of causing severe hand, foot and mouth disease (HFMD) associated with neurological complications and death. Currently, no FDA-approved antiviral is available for the treatment of EV-A71 infections. The flavonoid silymarin was shown to e...

Full description

Bibliographic Details
Main Authors: Lalani, S.*, Masomian, Malihe *, Poh, Chit Laa *
Format: Article
Language:English
Published: MDPI 2021
Subjects:
Online Access:http://eprints.sunway.edu.my/1836/
http://eprints.sunway.edu.my/1836/1/Malihe%20Masomian%20Functional%20insights%20into%20silymarin%20as%20an%20antiviral%20agent-ijms-22-08757%20%281%29.pdf
_version_ 1848802144535183360
author Lalani, S.*
Masomian, Malihe *
Poh, Chit Laa *
author_facet Lalani, S.*
Masomian, Malihe *
Poh, Chit Laa *
author_sort Lalani, S.*
building SU Institutional Repository
collection Online Access
description Enterovirus A71 (EV-A71) is a major neurovirulent agent capable of causing severe hand, foot and mouth disease (HFMD) associated with neurological complications and death. Currently, no FDA-approved antiviral is available for the treatment of EV-A71 infections. The flavonoid silymarin was shown to exert virucidal effects, but the binding site on the capsid was unknown. In this study, the ligand interacting site of silymarin was determined in silico and validated in vitro. Moreover, the potential of EV-A71 to develop resistance against silymarin was further evaluated. Molecular docking of silymarin with the capsid of EV-A71 indicated that silymarin binds to viral protein 1 (VP1) of EV-A71, specifically at the GH loop of VP1. The in vitro binding of silymarin with VP1 of EV-A71 was validated using recombinant VP1 through ELISA competitive binding assay. Continuous passaging of EV-A71 in the presence of silymarin resulted in the emergence of a mutant carrying a substitution of isoleucine by threonine (I97T) at position 97 of the BC loop of EV-A71. The mutation was speculated to overcome the inhibitory effects of silymarin. This study provides functional insights into the underlying mechanism of EV-A71 inhibition by silymarin, but warrants further in vivo evaluation before being developed as a potential therapeutic agent.
first_indexed 2025-11-14T21:18:41Z
format Article
id sunway-1836
institution Sunway University
institution_category Local University
language English
last_indexed 2025-11-14T21:18:41Z
publishDate 2021
publisher MDPI
recordtype eprints
repository_type Digital Repository
spelling sunway-18362021-08-23T07:55:52Z http://eprints.sunway.edu.my/1836/ Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71) Lalani, S.* Masomian, Malihe * Poh, Chit Laa * QR355 Virology Enterovirus A71 (EV-A71) is a major neurovirulent agent capable of causing severe hand, foot and mouth disease (HFMD) associated with neurological complications and death. Currently, no FDA-approved antiviral is available for the treatment of EV-A71 infections. The flavonoid silymarin was shown to exert virucidal effects, but the binding site on the capsid was unknown. In this study, the ligand interacting site of silymarin was determined in silico and validated in vitro. Moreover, the potential of EV-A71 to develop resistance against silymarin was further evaluated. Molecular docking of silymarin with the capsid of EV-A71 indicated that silymarin binds to viral protein 1 (VP1) of EV-A71, specifically at the GH loop of VP1. The in vitro binding of silymarin with VP1 of EV-A71 was validated using recombinant VP1 through ELISA competitive binding assay. Continuous passaging of EV-A71 in the presence of silymarin resulted in the emergence of a mutant carrying a substitution of isoleucine by threonine (I97T) at position 97 of the BC loop of EV-A71. The mutation was speculated to overcome the inhibitory effects of silymarin. This study provides functional insights into the underlying mechanism of EV-A71 inhibition by silymarin, but warrants further in vivo evaluation before being developed as a potential therapeutic agent. MDPI 2021-08 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/1836/1/Malihe%20Masomian%20Functional%20insights%20into%20silymarin%20as%20an%20antiviral%20agent-ijms-22-08757%20%281%29.pdf Lalani, S.* and Masomian, Malihe * and Poh, Chit Laa * (2021) Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71). International Journal of Molecular Sciences, 22 (16). p. 8757. ISSN 1422-0067 http://doi.org/10.3390/ijms22168757 doi:10.3390/ijms22168757
spellingShingle QR355 Virology
Lalani, S.*
Masomian, Malihe *
Poh, Chit Laa *
Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)
title Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)
title_full Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)
title_fullStr Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)
title_full_unstemmed Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)
title_short Functional insights into Silymarin as an antiviral agent against Enterovirus A71 (EV-A71)
title_sort functional insights into silymarin as an antiviral agent against enterovirus a71 (ev-a71)
topic QR355 Virology
url http://eprints.sunway.edu.my/1836/
http://eprints.sunway.edu.my/1836/
http://eprints.sunway.edu.my/1836/
http://eprints.sunway.edu.my/1836/1/Malihe%20Masomian%20Functional%20insights%20into%20silymarin%20as%20an%20antiviral%20agent-ijms-22-08757%20%281%29.pdf