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Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones

The increasing bacterial resistance to antibiotics is a worldwide concern. Essential oils are known to possess remarkable antibacterial properties, but their high chemical variability complicates their development into new antibacterial agents. Therefore, the main purpose of this study was to standa...

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Autores principales: Oliveira Ribeiro, Sofia, Fontaine, Véronique, Mathieu, Véronique, Abdesselam, Zhiri, Dominique, Baudoux, Caroline, Stévigny, Florence, Souard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156816/
https://www.ncbi.nlm.nih.gov/pubmed/34069154
http://dx.doi.org/10.3390/antibiotics10050584
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author Oliveira Ribeiro, Sofia
Fontaine, Véronique
Mathieu, Véronique
Abdesselam, Zhiri
Dominique, Baudoux
Caroline, Stévigny
Florence, Souard
author_facet Oliveira Ribeiro, Sofia
Fontaine, Véronique
Mathieu, Véronique
Abdesselam, Zhiri
Dominique, Baudoux
Caroline, Stévigny
Florence, Souard
author_sort Oliveira Ribeiro, Sofia
collection PubMed
description The increasing bacterial resistance to antibiotics is a worldwide concern. Essential oils are known to possess remarkable antibacterial properties, but their high chemical variability complicates their development into new antibacterial agents. Therefore, the main purpose of this study was to standardize their chemical composition. Several commercial essential oils of ajowan (Trachyspermum ammi L.) and thyme (chemotype thymol) (Thymus vulgaris L.) were bought on the market. GC–MS analysis revealed that thyme essential oils have a chemical composition far more consistent than ajowan essential oils. Sometimes thymol was not even the major compound. The most abundant compounds and the homemade mixtures were tested against two Staphylococcus aureus strains. The antibacterial property of β-caryophyllene presented no direct activity against S. aureus LMG 15975, but in association with thymol or carvacrol at equal percentages an MIC of 125 μg/mL was observed. The mixture of those three compounds at equivalent percentages also decreased by 16-fold the MIC of the penicillin V. Against S. aureus LMG 21674, β-caryophyllene presented an MIC of 31.3 μg/mL and decreased by 267-fold the MIC of the penicillin V. These observations led us to question the benefits of using a complex chemical mixture instead of one active compound to fight bacterial resistance.
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spelling pubmed-81568162021-05-28 Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones Oliveira Ribeiro, Sofia Fontaine, Véronique Mathieu, Véronique Abdesselam, Zhiri Dominique, Baudoux Caroline, Stévigny Florence, Souard Antibiotics (Basel) Article The increasing bacterial resistance to antibiotics is a worldwide concern. Essential oils are known to possess remarkable antibacterial properties, but their high chemical variability complicates their development into new antibacterial agents. Therefore, the main purpose of this study was to standardize their chemical composition. Several commercial essential oils of ajowan (Trachyspermum ammi L.) and thyme (chemotype thymol) (Thymus vulgaris L.) were bought on the market. GC–MS analysis revealed that thyme essential oils have a chemical composition far more consistent than ajowan essential oils. Sometimes thymol was not even the major compound. The most abundant compounds and the homemade mixtures were tested against two Staphylococcus aureus strains. The antibacterial property of β-caryophyllene presented no direct activity against S. aureus LMG 15975, but in association with thymol or carvacrol at equal percentages an MIC of 125 μg/mL was observed. The mixture of those three compounds at equivalent percentages also decreased by 16-fold the MIC of the penicillin V. Against S. aureus LMG 21674, β-caryophyllene presented an MIC of 31.3 μg/mL and decreased by 267-fold the MIC of the penicillin V. These observations led us to question the benefits of using a complex chemical mixture instead of one active compound to fight bacterial resistance. MDPI 2021-05-14 /pmc/articles/PMC8156816/ /pubmed/34069154 http://dx.doi.org/10.3390/antibiotics10050584 Text en © 2021 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
Oliveira Ribeiro, Sofia
Fontaine, Véronique
Mathieu, Véronique
Abdesselam, Zhiri
Dominique, Baudoux
Caroline, Stévigny
Florence, Souard
Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones
title Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones
title_full Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones
title_fullStr Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones
title_full_unstemmed Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones
title_short Antibacterial Activities of Homemade Matrices Miming Essential Oils Compared to Commercial Ones
title_sort antibacterial activities of homemade matrices miming essential oils compared to commercial ones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156816/
https://www.ncbi.nlm.nih.gov/pubmed/34069154
http://dx.doi.org/10.3390/antibiotics10050584
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