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Screening of Natural Products Inhibitors of SARS-CoV-2 Entry

The COVID-19 pandemic has led to the search for new molecules with antiviral activity against SARS-CoV-2. The entry of the virus into the cell is one of the main targets for inhibiting SARS-CoV-2 infection. Natural products are an important source of new therapeutic alternatives against diseases. Ps...

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Autores principales: González-Maldonado, Pamela, Alvarenga, Nelson, Burgos-Edwards, Alberto, Flores-Giubi, Ma. Eugenia, Barúa, Javier E., Romero-Rodríguez, Ma. Cristina, Soto-Rifo, Ricardo, Valiente-Echeverría, Fernando, Langjahr, Patricia, Cantero-González, Guadalupe, Sotelo, Pablo H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911944/
https://www.ncbi.nlm.nih.gov/pubmed/35268843
http://dx.doi.org/10.3390/molecules27051743
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author González-Maldonado, Pamela
Alvarenga, Nelson
Burgos-Edwards, Alberto
Flores-Giubi, Ma. Eugenia
Barúa, Javier E.
Romero-Rodríguez, Ma. Cristina
Soto-Rifo, Ricardo
Valiente-Echeverría, Fernando
Langjahr, Patricia
Cantero-González, Guadalupe
Sotelo, Pablo H.
author_facet González-Maldonado, Pamela
Alvarenga, Nelson
Burgos-Edwards, Alberto
Flores-Giubi, Ma. Eugenia
Barúa, Javier E.
Romero-Rodríguez, Ma. Cristina
Soto-Rifo, Ricardo
Valiente-Echeverría, Fernando
Langjahr, Patricia
Cantero-González, Guadalupe
Sotelo, Pablo H.
author_sort González-Maldonado, Pamela
collection PubMed
description The COVID-19 pandemic has led to the search for new molecules with antiviral activity against SARS-CoV-2. The entry of the virus into the cell is one of the main targets for inhibiting SARS-CoV-2 infection. Natural products are an important source of new therapeutic alternatives against diseases. Pseudotyped viruses allow the study of SARS-CoV-2 viral entry inhibitors, and due to their simplicity, they allow the screening of a large number of antiviral candidates in Biosafety Level 2 facilities. We used pseudotyped HIV-1 with the D614G SARS-CoV-2 spike glycoprotein to test its ability to infect ACE2-expressing HEK 293T cells in the presence of diverse natural products, including 21 plant extracts, 7 essential oils, and 13 compounds from plants and fungi. The 50% cytotoxic concentration (CC(50)) was evaluated using the resazurin method. From these analyses, we determined the inhibitory activity of the extract of Stachytarpheta cayennensis, which had a half-maximal inhibitory concentration (IC(50)) of 91.65 µg/mL, a CC(50) of 693.5 µg/mL, and a selectivity index (SI) of 7.57, indicating its potential use as an inhibitor of SARS-CoV-2 entry. Moreover, our work indicates the usefulness of the pseudotyped-virus system in the screening of SARS-CoV-2 entry inhibitors.
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spelling pubmed-89119442022-03-11 Screening of Natural Products Inhibitors of SARS-CoV-2 Entry González-Maldonado, Pamela Alvarenga, Nelson Burgos-Edwards, Alberto Flores-Giubi, Ma. Eugenia Barúa, Javier E. Romero-Rodríguez, Ma. Cristina Soto-Rifo, Ricardo Valiente-Echeverría, Fernando Langjahr, Patricia Cantero-González, Guadalupe Sotelo, Pablo H. Molecules Article The COVID-19 pandemic has led to the search for new molecules with antiviral activity against SARS-CoV-2. The entry of the virus into the cell is one of the main targets for inhibiting SARS-CoV-2 infection. Natural products are an important source of new therapeutic alternatives against diseases. Pseudotyped viruses allow the study of SARS-CoV-2 viral entry inhibitors, and due to their simplicity, they allow the screening of a large number of antiviral candidates in Biosafety Level 2 facilities. We used pseudotyped HIV-1 with the D614G SARS-CoV-2 spike glycoprotein to test its ability to infect ACE2-expressing HEK 293T cells in the presence of diverse natural products, including 21 plant extracts, 7 essential oils, and 13 compounds from plants and fungi. The 50% cytotoxic concentration (CC(50)) was evaluated using the resazurin method. From these analyses, we determined the inhibitory activity of the extract of Stachytarpheta cayennensis, which had a half-maximal inhibitory concentration (IC(50)) of 91.65 µg/mL, a CC(50) of 693.5 µg/mL, and a selectivity index (SI) of 7.57, indicating its potential use as an inhibitor of SARS-CoV-2 entry. Moreover, our work indicates the usefulness of the pseudotyped-virus system in the screening of SARS-CoV-2 entry inhibitors. MDPI 2022-03-07 /pmc/articles/PMC8911944/ /pubmed/35268843 http://dx.doi.org/10.3390/molecules27051743 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
González-Maldonado, Pamela
Alvarenga, Nelson
Burgos-Edwards, Alberto
Flores-Giubi, Ma. Eugenia
Barúa, Javier E.
Romero-Rodríguez, Ma. Cristina
Soto-Rifo, Ricardo
Valiente-Echeverría, Fernando
Langjahr, Patricia
Cantero-González, Guadalupe
Sotelo, Pablo H.
Screening of Natural Products Inhibitors of SARS-CoV-2 Entry
title Screening of Natural Products Inhibitors of SARS-CoV-2 Entry
title_full Screening of Natural Products Inhibitors of SARS-CoV-2 Entry
title_fullStr Screening of Natural Products Inhibitors of SARS-CoV-2 Entry
title_full_unstemmed Screening of Natural Products Inhibitors of SARS-CoV-2 Entry
title_short Screening of Natural Products Inhibitors of SARS-CoV-2 Entry
title_sort screening of natural products inhibitors of sars-cov-2 entry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911944/
https://www.ncbi.nlm.nih.gov/pubmed/35268843
http://dx.doi.org/10.3390/molecules27051743
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