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Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage
Streptococcus pyogenes is an important human pathogen worldwide. The identification of natural antibacterial phytochemicals has renewed interest due to the current scarcity of antibiotic development. Carvacrol is a monoterpenoid found in herbs. We evaluated carvacrol alone and combined with selected...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811018/ https://www.ncbi.nlm.nih.gov/pubmed/33452275 http://dx.doi.org/10.1038/s41598-020-79713-0 |
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author | Wijesundara, Niluni M. Lee, Song F. Cheng, Zhenyu Davidson, Ross Rupasinghe, H. P. Vasantha |
author_facet | Wijesundara, Niluni M. Lee, Song F. Cheng, Zhenyu Davidson, Ross Rupasinghe, H. P. Vasantha |
author_sort | Wijesundara, Niluni M. |
collection | PubMed |
description | Streptococcus pyogenes is an important human pathogen worldwide. The identification of natural antibacterial phytochemicals has renewed interest due to the current scarcity of antibiotic development. Carvacrol is a monoterpenoid found in herbs. We evaluated carvacrol alone and combined with selected antibiotics against four strains of S. pyogenes in vitro. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of carvacrol against S. pyogenes were 125 µg/mL (0.53 mM) and 250 µg/mL (1.05 mM), respectively. Kill curve results showed that carvacrol exhibits instantaneous bactericidal activity against S. pyogenes. We also demonstrated the potential mechanism of action of carvacrol through compromising the cell membrane integrity. Carvacrol induced membrane integrity changes leading to leakage of cytoplasmic content such as lactate dehydrogenase enzymes and nucleic acids. We further confirmed dose-dependent rupturing of cells and cell deaths using transmission electron microscopy. The chequerboard assay results showed that carvacrol possesses an additive-synergistic effect with clindamycin or penicillin. Carvacrol alone, combined with clindamycin or penicillin, can be used as a safe and efficacious natural health product for managing streptococcal pharyngitis. |
format | Online Article Text |
id | pubmed-7811018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78110182021-01-21 Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage Wijesundara, Niluni M. Lee, Song F. Cheng, Zhenyu Davidson, Ross Rupasinghe, H. P. Vasantha Sci Rep Article Streptococcus pyogenes is an important human pathogen worldwide. The identification of natural antibacterial phytochemicals has renewed interest due to the current scarcity of antibiotic development. Carvacrol is a monoterpenoid found in herbs. We evaluated carvacrol alone and combined with selected antibiotics against four strains of S. pyogenes in vitro. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of carvacrol against S. pyogenes were 125 µg/mL (0.53 mM) and 250 µg/mL (1.05 mM), respectively. Kill curve results showed that carvacrol exhibits instantaneous bactericidal activity against S. pyogenes. We also demonstrated the potential mechanism of action of carvacrol through compromising the cell membrane integrity. Carvacrol induced membrane integrity changes leading to leakage of cytoplasmic content such as lactate dehydrogenase enzymes and nucleic acids. We further confirmed dose-dependent rupturing of cells and cell deaths using transmission electron microscopy. The chequerboard assay results showed that carvacrol possesses an additive-synergistic effect with clindamycin or penicillin. Carvacrol alone, combined with clindamycin or penicillin, can be used as a safe and efficacious natural health product for managing streptococcal pharyngitis. Nature Publishing Group UK 2021-01-15 /pmc/articles/PMC7811018/ /pubmed/33452275 http://dx.doi.org/10.1038/s41598-020-79713-0 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Wijesundara, Niluni M. Lee, Song F. Cheng, Zhenyu Davidson, Ross Rupasinghe, H. P. Vasantha Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage |
title | Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage |
title_full | Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage |
title_fullStr | Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage |
title_full_unstemmed | Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage |
title_short | Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage |
title_sort | carvacrol exhibits rapid bactericidal activity against streptococcus pyogenes through cell membrane damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811018/ https://www.ncbi.nlm.nih.gov/pubmed/33452275 http://dx.doi.org/10.1038/s41598-020-79713-0 |
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