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In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms

BACKGROUND: Fungi are rich source of biologically active metabolites aimed for the improvement of human health through the prevention of various diseases, including infections and inflammatory disorders. AIM: We aimed to in vitro examine the anti-SARS CoV-2 activity of the aqueous extract of each Pl...

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Autores principales: Elhusseiny, Shaza M, El-Mahdy, Taghrid S, Elleboudy, Nooran S, Yahia, Ibrahim S, Farag, Mohamed M S, Ismail, Nasser S M, Yassien, Mahmoud A, Aboshanab, Khaled M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259418/
https://www.ncbi.nlm.nih.gov/pubmed/35813084
http://dx.doi.org/10.2147/IDR.S362823
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author Elhusseiny, Shaza M
El-Mahdy, Taghrid S
Elleboudy, Nooran S
Yahia, Ibrahim S
Farag, Mohamed M S
Ismail, Nasser S M
Yassien, Mahmoud A
Aboshanab, Khaled M
author_facet Elhusseiny, Shaza M
El-Mahdy, Taghrid S
Elleboudy, Nooran S
Yahia, Ibrahim S
Farag, Mohamed M S
Ismail, Nasser S M
Yassien, Mahmoud A
Aboshanab, Khaled M
author_sort Elhusseiny, Shaza M
collection PubMed
description BACKGROUND: Fungi are rich source of biologically active metabolites aimed for the improvement of human health through the prevention of various diseases, including infections and inflammatory disorders. AIM: We aimed to in vitro examine the anti-SARS CoV-2 activity of the aqueous extract of each Pleurotus (P.) ostreatus, Lentinula (L.) edodes and Agaricus (A.) bisporus edible mushroom followed by docking analysis of certain metabolites against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-main protease (protease M(pro)). METHODS: Antiviral and cytotoxic effects were tested on hCoV-19/Egypt/NRC-3/2020/Vero-E6 cells and analyzed via (3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide Assay (MTT) assay. Ligand-protein and protein-protein docking studies were performed to explore the interaction of different mushroom extracts at the binding site of protease M(pro). Molecular dynamics (MD) simulations were performed on the most promising ligand-target complexes to investigate their dynamic properties and confirm docking results. RESULTS: Substantial antiviral activities with an IC(50) of 39.19, 26.17, and 10.3.3 µg/mL and a selectivity index (SI) of 4.34, 3.44, and 1.5 for P. ostreatus, L. edodes and A. bisporus, were observed, respectively. Docking analysis revealed that, catechin from three mushroom isolates, chlorogenic acid from A. bisporus, kamperferol of P. ostreatus and quercetin from L. edodes, with a C-DOCKER interaction energy in the range of 22.8–37.61 (Kcal/mol) with protease compared to boceprevir ligand of 41.6 (Kcal/mol). Docking of superoxide dismutase, catalase from the three mushrooms, tyrosinase from A. bisporus showed ligand contact surface area with the protein as 252.74 Å(2) while receptor contact surface area was 267.23 Å(2). CONCLUSION: P. ostreatus, L. edodes and A. bisporus have potential and remarkable in vitro antiviral activities against SARS-CoV-2. Quercetin from L. edodes, Kaempferol from P. ostreatus, chlorogenic acid and ascorbic acid, catechin, superoxide dismutase and catalase of the three mushrooms extracts were effectively bounded to M(pro) of SARS-CoV-2 as conferred by docking analysis.
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spelling pubmed-92594182022-07-08 In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms Elhusseiny, Shaza M El-Mahdy, Taghrid S Elleboudy, Nooran S Yahia, Ibrahim S Farag, Mohamed M S Ismail, Nasser S M Yassien, Mahmoud A Aboshanab, Khaled M Infect Drug Resist Original Research BACKGROUND: Fungi are rich source of biologically active metabolites aimed for the improvement of human health through the prevention of various diseases, including infections and inflammatory disorders. AIM: We aimed to in vitro examine the anti-SARS CoV-2 activity of the aqueous extract of each Pleurotus (P.) ostreatus, Lentinula (L.) edodes and Agaricus (A.) bisporus edible mushroom followed by docking analysis of certain metabolites against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-main protease (protease M(pro)). METHODS: Antiviral and cytotoxic effects were tested on hCoV-19/Egypt/NRC-3/2020/Vero-E6 cells and analyzed via (3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide Assay (MTT) assay. Ligand-protein and protein-protein docking studies were performed to explore the interaction of different mushroom extracts at the binding site of protease M(pro). Molecular dynamics (MD) simulations were performed on the most promising ligand-target complexes to investigate their dynamic properties and confirm docking results. RESULTS: Substantial antiviral activities with an IC(50) of 39.19, 26.17, and 10.3.3 µg/mL and a selectivity index (SI) of 4.34, 3.44, and 1.5 for P. ostreatus, L. edodes and A. bisporus, were observed, respectively. Docking analysis revealed that, catechin from three mushroom isolates, chlorogenic acid from A. bisporus, kamperferol of P. ostreatus and quercetin from L. edodes, with a C-DOCKER interaction energy in the range of 22.8–37.61 (Kcal/mol) with protease compared to boceprevir ligand of 41.6 (Kcal/mol). Docking of superoxide dismutase, catalase from the three mushrooms, tyrosinase from A. bisporus showed ligand contact surface area with the protein as 252.74 Å(2) while receptor contact surface area was 267.23 Å(2). CONCLUSION: P. ostreatus, L. edodes and A. bisporus have potential and remarkable in vitro antiviral activities against SARS-CoV-2. Quercetin from L. edodes, Kaempferol from P. ostreatus, chlorogenic acid and ascorbic acid, catechin, superoxide dismutase and catalase of the three mushrooms extracts were effectively bounded to M(pro) of SARS-CoV-2 as conferred by docking analysis. Dove 2022-07-02 /pmc/articles/PMC9259418/ /pubmed/35813084 http://dx.doi.org/10.2147/IDR.S362823 Text en © 2022 Elhusseiny et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Elhusseiny, Shaza M
El-Mahdy, Taghrid S
Elleboudy, Nooran S
Yahia, Ibrahim S
Farag, Mohamed M S
Ismail, Nasser S M
Yassien, Mahmoud A
Aboshanab, Khaled M
In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms
title In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms
title_full In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms
title_fullStr In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms
title_full_unstemmed In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms
title_short In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms
title_sort in vitro anti sars-cov-2 activity and docking analysis of pleurotus ostreatus, lentinula edodes and agaricus bisporus edible mushrooms
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259418/
https://www.ncbi.nlm.nih.gov/pubmed/35813084
http://dx.doi.org/10.2147/IDR.S362823
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