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In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2

In 2019, coronavirus has made the third apparition in the form of SARS-CoV-2, a novel strain of coronavirus that is extremely pathogenic and it uses the same receptor as SARS-CoV, the angiotensin-converting enzyme 2 (ACE2). However, more than 182 vaccine candidates have been announced; and 12 vaccin...

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Autores principales: Matsabisa, M. G., Alexandre, K., Ibeji, Collins U., Tripathy, S., Erukainure, Ochuko L., Malatji, K., Chauke, S., Okole, B., Chabalala, H. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207029/
https://www.ncbi.nlm.nih.gov/pubmed/35718800
http://dx.doi.org/10.1038/s41598-022-13599-y
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author Matsabisa, M. G.
Alexandre, K.
Ibeji, Collins U.
Tripathy, S.
Erukainure, Ochuko L.
Malatji, K.
Chauke, S.
Okole, B.
Chabalala, H. P.
author_facet Matsabisa, M. G.
Alexandre, K.
Ibeji, Collins U.
Tripathy, S.
Erukainure, Ochuko L.
Malatji, K.
Chauke, S.
Okole, B.
Chabalala, H. P.
author_sort Matsabisa, M. G.
collection PubMed
description In 2019, coronavirus has made the third apparition in the form of SARS-CoV-2, a novel strain of coronavirus that is extremely pathogenic and it uses the same receptor as SARS-CoV, the angiotensin-converting enzyme 2 (ACE2). However, more than 182 vaccine candidates have been announced; and 12 vaccines have been approved for use, although, even vaccinated individuals are still vulnerable to infection. In this study, we investigated PHELA, recognized as an herbal combination of four exotic African medicinal plants namely; Clerodendrum glabrum E. Mey. Lamiaceae, Gladiolus dalenii van Geel, Rotheca myricoides (Hochst.) Steane & Mabb, and Senna occidentalis (L.) Link; as a candidate therapy for COVID-19. In vitro testing found that PHELA inhibited > 90% of SARS-CoV-2 and SARS-CoV infection at concentration levels of 0.005 mg/ml to 0.03 mg/ml and close to 100% of MERS-CoV infection at 0.1 mg/ml to 0.6 mg/ml. The in vitro average IC(50) of PHELA on SARS-COV-2, SARS-CoV and MERS-COV were ~ 0.01 mg/ml. Secondly in silico docking studies of compounds identified in PHELA showed very strong binding energy interactions with the SARS-COV-2 proteins. Compound 5 showed the highest affinity for SARS-COV-2 protein compared to other compounds with the binding energy of − 6.8 kcal mol(−1). Our data showed that PHELA has potential and could be developed as a COVID-19 therapeutic.
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spelling pubmed-92070292022-06-21 In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2 Matsabisa, M. G. Alexandre, K. Ibeji, Collins U. Tripathy, S. Erukainure, Ochuko L. Malatji, K. Chauke, S. Okole, B. Chabalala, H. P. Sci Rep Article In 2019, coronavirus has made the third apparition in the form of SARS-CoV-2, a novel strain of coronavirus that is extremely pathogenic and it uses the same receptor as SARS-CoV, the angiotensin-converting enzyme 2 (ACE2). However, more than 182 vaccine candidates have been announced; and 12 vaccines have been approved for use, although, even vaccinated individuals are still vulnerable to infection. In this study, we investigated PHELA, recognized as an herbal combination of four exotic African medicinal plants namely; Clerodendrum glabrum E. Mey. Lamiaceae, Gladiolus dalenii van Geel, Rotheca myricoides (Hochst.) Steane & Mabb, and Senna occidentalis (L.) Link; as a candidate therapy for COVID-19. In vitro testing found that PHELA inhibited > 90% of SARS-CoV-2 and SARS-CoV infection at concentration levels of 0.005 mg/ml to 0.03 mg/ml and close to 100% of MERS-CoV infection at 0.1 mg/ml to 0.6 mg/ml. The in vitro average IC(50) of PHELA on SARS-COV-2, SARS-CoV and MERS-COV were ~ 0.01 mg/ml. Secondly in silico docking studies of compounds identified in PHELA showed very strong binding energy interactions with the SARS-COV-2 proteins. Compound 5 showed the highest affinity for SARS-COV-2 protein compared to other compounds with the binding energy of − 6.8 kcal mol(−1). Our data showed that PHELA has potential and could be developed as a COVID-19 therapeutic. Nature Publishing Group UK 2022-06-19 /pmc/articles/PMC9207029/ /pubmed/35718800 http://dx.doi.org/10.1038/s41598-022-13599-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Matsabisa, M. G.
Alexandre, K.
Ibeji, Collins U.
Tripathy, S.
Erukainure, Ochuko L.
Malatji, K.
Chauke, S.
Okole, B.
Chabalala, H. P.
In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2
title In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2
title_full In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2
title_fullStr In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2
title_full_unstemmed In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2
title_short In vitro study on efficacy of PHELA, an African traditional drug against SARS-CoV-2
title_sort in vitro study on efficacy of phela, an african traditional drug against sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207029/
https://www.ncbi.nlm.nih.gov/pubmed/35718800
http://dx.doi.org/10.1038/s41598-022-13599-y
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