In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2

In spite of the large number of repositioned drugs and direct-acting antivirals in clinical trials for the management of the ongoing COVID-19 pandemic, there are few cost-effective therapeutic options for severe acute respiratory syndrome (SARS) coronavirus 2 (SCoV2) infection. In this paper, we sho...

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Autores principales: Minwoo Kim, Hee Cho, Dae-Gyun Ahn, Hae-Gwang Jung, Han Young Seo, Ji-Su Kim, Youn-Jung Lee, Jun Yong Choi, In Ho Park, Jeon-Soo Shin, Seong-Jun Kim, Jong-Won Oh
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/937bed01cc4a41f99ba2c4b884aae531
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spelling oai:doaj.org-article:937bed01cc4a41f99ba2c4b884aae5312021-11-25T16:51:25ZIn Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 210.3390/biomedicines91117252227-9059https://doaj.org/article/937bed01cc4a41f99ba2c4b884aae5312021-11-01T00:00:00Zhttps://www.mdpi.com/2227-9059/9/11/1725https://doaj.org/toc/2227-9059In spite of the large number of repositioned drugs and direct-acting antivirals in clinical trials for the management of the ongoing COVID-19 pandemic, there are few cost-effective therapeutic options for severe acute respiratory syndrome (SARS) coronavirus 2 (SCoV2) infection. In this paper, we show that xanthorrhizol (XNT), a bisabolane-type sesquiterpenoid compound isolated from the <i>Curcuma xanthorrhizza</i> Roxb., a ginger-line plant of the family <i>Zingiberaceae</i>, displays a potent antiviral efficacy in vitro against SCoV2 and other related coronaviruses, including SARS-CoV-1 (SCoV1) and a common cold-causing human coronavirus. XNT reduced infectious SCoV2 titer by ~3-log<sub>10</sub> at 20 μM and interfered with the replication of the SCoV1 subgenomic replicon, while it had no significant antiviral effects against hepatitis C virus and noroviruses. Further, XNT exerted similar antiviral functions against SCoV2 variants, such as a GH clade strain and a delta strain currently predominant worldwide. Neither SCoV2 entry into cells nor the enzymatic activity of viral RNA polymerase (Nsp12), RNA helicase (Nsp13), or the 3CL main protease (Nsp5) was inhibited by XNT. While its CoV replication inhibitory mechanism remains elusive, our results demonstrate that the traditional folk medicine XNT could be a promising antiviral candidate that inhibits a broad range of SCoV2 variants of concern and other related CoVs.Minwoo KimHee ChoDae-Gyun AhnHae-Gwang JungHan Young SeoJi-Su KimYoun-Jung LeeJun Yong ChoiIn Ho ParkJeon-Soo ShinSeong-Jun KimJong-Won OhMDPI AGarticleSARS-CoV-2xanthorrhizolpan-coronavirus antiviralsherbal medicineSARS-CoV-1human coronavirusBiology (General)QH301-705.5ENBiomedicines, Vol 9, Iss 1725, p 1725 (2021)
institution DOAJ
collection DOAJ
language EN
topic SARS-CoV-2
xanthorrhizol
pan-coronavirus antivirals
herbal medicine
SARS-CoV-1
human coronavirus
Biology (General)
QH301-705.5
spellingShingle SARS-CoV-2
xanthorrhizol
pan-coronavirus antivirals
herbal medicine
SARS-CoV-1
human coronavirus
Biology (General)
QH301-705.5
Minwoo Kim
Hee Cho
Dae-Gyun Ahn
Hae-Gwang Jung
Han Young Seo
Ji-Su Kim
Youn-Jung Lee
Jun Yong Choi
In Ho Park
Jeon-Soo Shin
Seong-Jun Kim
Jong-Won Oh
In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2
description In spite of the large number of repositioned drugs and direct-acting antivirals in clinical trials for the management of the ongoing COVID-19 pandemic, there are few cost-effective therapeutic options for severe acute respiratory syndrome (SARS) coronavirus 2 (SCoV2) infection. In this paper, we show that xanthorrhizol (XNT), a bisabolane-type sesquiterpenoid compound isolated from the <i>Curcuma xanthorrhizza</i> Roxb., a ginger-line plant of the family <i>Zingiberaceae</i>, displays a potent antiviral efficacy in vitro against SCoV2 and other related coronaviruses, including SARS-CoV-1 (SCoV1) and a common cold-causing human coronavirus. XNT reduced infectious SCoV2 titer by ~3-log<sub>10</sub> at 20 μM and interfered with the replication of the SCoV1 subgenomic replicon, while it had no significant antiviral effects against hepatitis C virus and noroviruses. Further, XNT exerted similar antiviral functions against SCoV2 variants, such as a GH clade strain and a delta strain currently predominant worldwide. Neither SCoV2 entry into cells nor the enzymatic activity of viral RNA polymerase (Nsp12), RNA helicase (Nsp13), or the 3CL main protease (Nsp5) was inhibited by XNT. While its CoV replication inhibitory mechanism remains elusive, our results demonstrate that the traditional folk medicine XNT could be a promising antiviral candidate that inhibits a broad range of SCoV2 variants of concern and other related CoVs.
format article
author Minwoo Kim
Hee Cho
Dae-Gyun Ahn
Hae-Gwang Jung
Han Young Seo
Ji-Su Kim
Youn-Jung Lee
Jun Yong Choi
In Ho Park
Jeon-Soo Shin
Seong-Jun Kim
Jong-Won Oh
author_facet Minwoo Kim
Hee Cho
Dae-Gyun Ahn
Hae-Gwang Jung
Han Young Seo
Ji-Su Kim
Youn-Jung Lee
Jun Yong Choi
In Ho Park
Jeon-Soo Shin
Seong-Jun Kim
Jong-Won Oh
author_sort Minwoo Kim
title In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2
title_short In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2
title_full In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2
title_fullStr In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2
title_full_unstemmed In Vitro Replication Inhibitory Activity of Xanthorrhizol against Severe Acute Respiratory Syndrome Coronavirus 2
title_sort in vitro replication inhibitory activity of xanthorrhizol against severe acute respiratory syndrome coronavirus 2
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/937bed01cc4a41f99ba2c4b884aae531
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