The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro

The coronavirus disease 2019 (COVID-19), caused by a novel coronavirus (SARS-CoV-2), has spread worldwide, affecting over 250 million people and resulting in over five million deaths. Antivirals that are effective are still limited. The antiviral activities of the <i>Petasites hybdridus</i&...

Full description

Bibliographic Details
Main Authors: Lorena Urda, Matthias Heinrich Kreuter, Jürgen Drewe, Georg Boonen, Veronika Butterweck, Thomas Klimkait
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/14/1/106
_version_ 1797489743695446016
author Lorena Urda
Matthias Heinrich Kreuter
Jürgen Drewe
Georg Boonen
Veronika Butterweck
Thomas Klimkait
author_facet Lorena Urda
Matthias Heinrich Kreuter
Jürgen Drewe
Georg Boonen
Veronika Butterweck
Thomas Klimkait
author_sort Lorena Urda
collection DOAJ
description The coronavirus disease 2019 (COVID-19), caused by a novel coronavirus (SARS-CoV-2), has spread worldwide, affecting over 250 million people and resulting in over five million deaths. Antivirals that are effective are still limited. The antiviral activities of the <i>Petasites hybdridus</i> CO<sub>2</sub> extract Ze 339 were previously reported. Thus, to assess the anti-SARS-CoV-2 activity of Ze 339 as well as isopetasin and neopetasin as major active compounds, a CPE and plaque reduction assay in Vero E6 cells was used for viral output. Antiviral effects were tested using the original virus (Wuhan) and the Delta variant of SARS-CoV-2. The antiviral drug remdesivir was used as control. Pre-treatment with Ze 339 in SARS-CoV-2-infected Vero E6 cells with either virus variant significantly inhibited virus replication with IC<sub>50</sub> values of 0.10 and 0.40 μg/mL, respectively. The IC<sub>50</sub> values obtained for isopetasin ranged between 0.37 and 0.88 μM for both virus variants, and that of remdesivir ranged between 1.53 and 2.37 μM. In conclusion, Ze 339 as well as the petasins potently inhibited SARS-CoV-2 replication in vitro of the Wuhan and Delta variants. Since time is of essence in finding effective treatments, clinical studies will have to demonstrate if Ze339 can become a therapeutic option to treat SARS-CoV-2 infections.
first_indexed 2024-03-10T00:21:01Z
format Article
id doaj.art-98e9e24048f3488d921e4e78a0049821
institution Directory Open Access Journal
issn 1999-4915
language English
last_indexed 2024-03-10T00:21:01Z
publishDate 2022-01-01
publisher MDPI AG
record_format Article
series Viruses
spelling doaj.art-98e9e24048f3488d921e4e78a00498212023-11-23T15:42:19ZengMDPI AGViruses1999-49152022-01-0114110610.3390/v14010106The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In VitroLorena Urda0Matthias Heinrich Kreuter1Jürgen Drewe2Georg Boonen3Veronika Butterweck4Thomas Klimkait5Department Biomedicine, University of Basel, Petersplatz 10, 4051 Basel, SwitzerlandMedical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, SwitzerlandMedical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, SwitzerlandMedical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, SwitzerlandMedical Department, Max Zeller & Söhne AG, Seeblickstrasse 4, 8590 Romanshorn, SwitzerlandDepartment Biomedicine, University of Basel, Petersplatz 10, 4051 Basel, SwitzerlandThe coronavirus disease 2019 (COVID-19), caused by a novel coronavirus (SARS-CoV-2), has spread worldwide, affecting over 250 million people and resulting in over five million deaths. Antivirals that are effective are still limited. The antiviral activities of the <i>Petasites hybdridus</i> CO<sub>2</sub> extract Ze 339 were previously reported. Thus, to assess the anti-SARS-CoV-2 activity of Ze 339 as well as isopetasin and neopetasin as major active compounds, a CPE and plaque reduction assay in Vero E6 cells was used for viral output. Antiviral effects were tested using the original virus (Wuhan) and the Delta variant of SARS-CoV-2. The antiviral drug remdesivir was used as control. Pre-treatment with Ze 339 in SARS-CoV-2-infected Vero E6 cells with either virus variant significantly inhibited virus replication with IC<sub>50</sub> values of 0.10 and 0.40 μg/mL, respectively. The IC<sub>50</sub> values obtained for isopetasin ranged between 0.37 and 0.88 μM for both virus variants, and that of remdesivir ranged between 1.53 and 2.37 μM. In conclusion, Ze 339 as well as the petasins potently inhibited SARS-CoV-2 replication in vitro of the Wuhan and Delta variants. Since time is of essence in finding effective treatments, clinical studies will have to demonstrate if Ze339 can become a therapeutic option to treat SARS-CoV-2 infections.https://www.mdpi.com/1999-4915/14/1/106SARS-CoV-2COVID-19anti-COVID-19antiviralDelta variant<i>Petasites hybridus</i>
spellingShingle Lorena Urda
Matthias Heinrich Kreuter
Jürgen Drewe
Georg Boonen
Veronika Butterweck
Thomas Klimkait
The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro
Viruses
SARS-CoV-2
COVID-19
anti-COVID-19
antiviral
Delta variant
<i>Petasites hybridus</i>
title The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro
title_full The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro
title_fullStr The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro
title_full_unstemmed The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro
title_short The <i>Petasites hybridus</i> CO<sub>2</sub> Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro
title_sort i petasites hybridus i co sub 2 sub extract ze 339 blocks sars cov 2 replication in vitro
topic SARS-CoV-2
COVID-19
anti-COVID-19
antiviral
Delta variant
<i>Petasites hybridus</i>
url https://www.mdpi.com/1999-4915/14/1/106
work_keys_str_mv AT lorenaurda theipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT matthiasheinrichkreuter theipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT jurgendrewe theipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT georgboonen theipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT veronikabutterweck theipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT thomasklimkait theipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT lorenaurda ipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT matthiasheinrichkreuter ipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT jurgendrewe ipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT georgboonen ipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT veronikabutterweck ipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro
AT thomasklimkait ipetasiteshybridusicosub2subextractze339blockssarscov2replicationinvitro