Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro

IntroductionThe Getah virus (GETV) is a zoonotic arbovirus causing disease in humans and animals, a member of the Alphavirus genus. Currently, approved antiviral drugs and vaccines against alphaviruses are few available. This study aimed to investigate the anti-GETV activity of the Extract of Scutel...

Full description

Saved in:
Bibliographic Details
Main Authors: Baoling Liu, Yuling Wang, Lina Shao, Yuanhang Chen, Zhiwen Xu, Ling Zhu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Veterinary Science
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fvets.2025.1551501/full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850099093235302400
author Baoling Liu
Yuling Wang
Lina Shao
Yuanhang Chen
Zhiwen Xu
Zhiwen Xu
Ling Zhu
Ling Zhu
author_facet Baoling Liu
Yuling Wang
Lina Shao
Yuanhang Chen
Zhiwen Xu
Zhiwen Xu
Ling Zhu
Ling Zhu
author_sort Baoling Liu
collection DOAJ
description IntroductionThe Getah virus (GETV) is a zoonotic arbovirus causing disease in humans and animals, a member of the Alphavirus genus. Currently, approved antiviral drugs and vaccines against alphaviruses are few available. This study aimed to investigate the anti-GETV activity of the Extract of Scutellaria baicalensis Georgi (ESG) in vivo and in vitro.MethodsThe cytotoxic effects of ESG on BHK-21 cells were quantitatively evaluated through the MTT assay. Quantitative analysis of viral replication was performed using qRT-PCR, while E2 protein expression was analyzed through western blotting. Furthermore, molecular docking simulations were conducted to examine the binding affinity between the principal bioactive constituents of ESG and the E2 structural proteins. Additionally, the therapeutic potential of ESG in alleviating viremia was evaluated in GETV-infected mouse models.ResultsThe results showed that ESG significantly attenuated the cytopathic effects induced by GETV infection in BHK-21 cells, concurrently reducing both viral replication and E2 protein expression. Notably, ESG exhibited its most potent antiviral activity during the viral attachment and entry phases, with IC50 values of 3.69 μg/mL and 3.94 μg/mL, respectively. At a concentration of 10 μg/mL, ESG achieved 95.08% inhibition efficiency against viral attachment. Furthermore, in vivo studies revealed that ESG treatment significantly reduced the peak viral load and shortened the duration of viremia in GETV-infected mice. The main components of ESG are baicalin and baicalein, and molecular docking simulations demonstrated strong binding affinities between these compounds and the active site of GETV E2 protein, with docking scores of −6.99 kcal/mol for baicalin and −5.21 kcal/mol for baicalein.ConclusionThe experimental findings demonstrate that ESG exhibits significant antiviral efficacy against GETV infection both in vitro and in vivo. These results indicate that ESG represents a promising therapeutic candidate for the prevention and treatment of GETV infections. Mechanistically, the antiviral activity of ESG appears to be mediated, at least in part, through the modulation of E2 protein expression.
format Article
id doaj-art-f67b078d5f7a43a6a2b37e9a8c04baf7
institution DOAJ
issn 2297-1769
language English
publishDate 2025-03-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Veterinary Science
spelling doaj-art-f67b078d5f7a43a6a2b37e9a8c04baf72025-08-20T02:40:34ZengFrontiers Media S.A.Frontiers in Veterinary Science2297-17692025-03-011210.3389/fvets.2025.15515011551501Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitroBaoling Liu0Yuling Wang1Lina Shao2Yuanhang Chen3Zhiwen Xu4Zhiwen Xu5Ling Zhu6Ling Zhu7College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, ChinaSichuan Key Laboratory of Animal Epidemic Disease and Human Health, Sichuan Agricultural University, Chengdu, ChinaCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, ChinaSichuan Key Laboratory of Animal Epidemic Disease and Human Health, Sichuan Agricultural University, Chengdu, ChinaIntroductionThe Getah virus (GETV) is a zoonotic arbovirus causing disease in humans and animals, a member of the Alphavirus genus. Currently, approved antiviral drugs and vaccines against alphaviruses are few available. This study aimed to investigate the anti-GETV activity of the Extract of Scutellaria baicalensis Georgi (ESG) in vivo and in vitro.MethodsThe cytotoxic effects of ESG on BHK-21 cells were quantitatively evaluated through the MTT assay. Quantitative analysis of viral replication was performed using qRT-PCR, while E2 protein expression was analyzed through western blotting. Furthermore, molecular docking simulations were conducted to examine the binding affinity between the principal bioactive constituents of ESG and the E2 structural proteins. Additionally, the therapeutic potential of ESG in alleviating viremia was evaluated in GETV-infected mouse models.ResultsThe results showed that ESG significantly attenuated the cytopathic effects induced by GETV infection in BHK-21 cells, concurrently reducing both viral replication and E2 protein expression. Notably, ESG exhibited its most potent antiviral activity during the viral attachment and entry phases, with IC50 values of 3.69 μg/mL and 3.94 μg/mL, respectively. At a concentration of 10 μg/mL, ESG achieved 95.08% inhibition efficiency against viral attachment. Furthermore, in vivo studies revealed that ESG treatment significantly reduced the peak viral load and shortened the duration of viremia in GETV-infected mice. The main components of ESG are baicalin and baicalein, and molecular docking simulations demonstrated strong binding affinities between these compounds and the active site of GETV E2 protein, with docking scores of −6.99 kcal/mol for baicalin and −5.21 kcal/mol for baicalein.ConclusionThe experimental findings demonstrate that ESG exhibits significant antiviral efficacy against GETV infection both in vitro and in vivo. These results indicate that ESG represents a promising therapeutic candidate for the prevention and treatment of GETV infections. Mechanistically, the antiviral activity of ESG appears to be mediated, at least in part, through the modulation of E2 protein expression.https://www.frontiersin.org/articles/10.3389/fvets.2025.1551501/fullantiviralScutellaria baicalensis Georgi ExtractGetah virusnatural compoundstraditional Chinese medicine
spellingShingle Baoling Liu
Yuling Wang
Lina Shao
Yuanhang Chen
Zhiwen Xu
Zhiwen Xu
Ling Zhu
Ling Zhu
Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro
Frontiers in Veterinary Science
antiviral
Scutellaria baicalensis Georgi Extract
Getah virus
natural compounds
traditional Chinese medicine
title Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro
title_full Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro
title_fullStr Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro
title_full_unstemmed Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro
title_short Antiviral activity of Scutellaria baicalensis Georgi Extract against Getah virus in vivo and in vitro
title_sort antiviral activity of scutellaria baicalensis georgi extract against getah virus in vivo and in vitro
topic antiviral
Scutellaria baicalensis Georgi Extract
Getah virus
natural compounds
traditional Chinese medicine
url https://www.frontiersin.org/articles/10.3389/fvets.2025.1551501/full
work_keys_str_mv AT baolingliu antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT yulingwang antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT linashao antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT yuanhangchen antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT zhiwenxu antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT zhiwenxu antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT lingzhu antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro
AT lingzhu antiviralactivityofscutellariabaicalensisgeorgiextractagainstgetahvirusinvivoandinvitro