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Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates

Much effort has focused on examining the inhibitory effect of Salvadora persica (miswak) on oral microorganisms, but information concerning its antibacterial activity against other human pathogens, particularly multidrug resistant (MDR) isolates, is scarce. Therefore, this study aimed to assess the...

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Autores principales: Al-Ayed, Mohamed Saeed Zayed, Asaad, Ahmed Morad, Qureshi, Mohamed Ansar, Attia, Hany Goda, AlMarrani, Abduljabbar Hadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745819/
https://www.ncbi.nlm.nih.gov/pubmed/26904146
http://dx.doi.org/10.1155/2016/7083964
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author Al-Ayed, Mohamed Saeed Zayed
Asaad, Ahmed Morad
Qureshi, Mohamed Ansar
Attia, Hany Goda
AlMarrani, Abduljabbar Hadi
author_facet Al-Ayed, Mohamed Saeed Zayed
Asaad, Ahmed Morad
Qureshi, Mohamed Ansar
Attia, Hany Goda
AlMarrani, Abduljabbar Hadi
author_sort Al-Ayed, Mohamed Saeed Zayed
collection PubMed
description Much effort has focused on examining the inhibitory effect of Salvadora persica (miswak) on oral microorganisms, but information concerning its antibacterial activity against other human pathogens, particularly multidrug resistant (MDR) isolates, is scarce. Therefore, this study aimed to assess the in vitro antibacterial activities of Salvadora persica L. extracts against 10 MDR bacterial clinical isolates other than oral pathogens. The antibacterial activity of aqueous and methanol miswak extracts was assessed using the agar dilution and minimum inhibitory concentration (MIC) methods. Overall, the 400 mg/mL of miswak extract was the most effective on all strains. The methanol extract exhibited a stronger antibacterial activity against Gram-negative (3.3–13.6 mm) than Gram-positive (1.8–8.3 mm) bacteria. The lowest MIC value was seen for E. coli (0.39, 1.56 µg/mL), followed by Streptococcus pyogenes (1.56 µg/mL). The highest MIC value (6.25, 12.5 µg/mL) was recorded for methicillin-resistant Staphylococcus aureus (MRSA), Acinetobacter baumannii, and Stenotrophomonas maltophilia. This study demonstrates, for the first time, the moderate to strong antibacterial activity of miswak extracts against all tested MDR-pathogens. Methanol extract appears to be a potent antimicrobial agent that could be considered as complementary and alternative medicine against resistant pathogens. Further studies on a large number of MDR organisms are necessary to investigate and standardize the inhibitory effect of miswak extracts against these emerging pathogens.
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spelling pubmed-47458192016-02-22 Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates Al-Ayed, Mohamed Saeed Zayed Asaad, Ahmed Morad Qureshi, Mohamed Ansar Attia, Hany Goda AlMarrani, Abduljabbar Hadi Evid Based Complement Alternat Med Research Article Much effort has focused on examining the inhibitory effect of Salvadora persica (miswak) on oral microorganisms, but information concerning its antibacterial activity against other human pathogens, particularly multidrug resistant (MDR) isolates, is scarce. Therefore, this study aimed to assess the in vitro antibacterial activities of Salvadora persica L. extracts against 10 MDR bacterial clinical isolates other than oral pathogens. The antibacterial activity of aqueous and methanol miswak extracts was assessed using the agar dilution and minimum inhibitory concentration (MIC) methods. Overall, the 400 mg/mL of miswak extract was the most effective on all strains. The methanol extract exhibited a stronger antibacterial activity against Gram-negative (3.3–13.6 mm) than Gram-positive (1.8–8.3 mm) bacteria. The lowest MIC value was seen for E. coli (0.39, 1.56 µg/mL), followed by Streptococcus pyogenes (1.56 µg/mL). The highest MIC value (6.25, 12.5 µg/mL) was recorded for methicillin-resistant Staphylococcus aureus (MRSA), Acinetobacter baumannii, and Stenotrophomonas maltophilia. This study demonstrates, for the first time, the moderate to strong antibacterial activity of miswak extracts against all tested MDR-pathogens. Methanol extract appears to be a potent antimicrobial agent that could be considered as complementary and alternative medicine against resistant pathogens. Further studies on a large number of MDR organisms are necessary to investigate and standardize the inhibitory effect of miswak extracts against these emerging pathogens. Hindawi Publishing Corporation 2016 2016-01-19 /pmc/articles/PMC4745819/ /pubmed/26904146 http://dx.doi.org/10.1155/2016/7083964 Text en Copyright © 2016 Mohamed Saeed Zayed Al-Ayed et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Al-Ayed, Mohamed Saeed Zayed
Asaad, Ahmed Morad
Qureshi, Mohamed Ansar
Attia, Hany Goda
AlMarrani, Abduljabbar Hadi
Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates
title Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates
title_full Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates
title_fullStr Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates
title_full_unstemmed Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates
title_short Antibacterial Activity of Salvadora persica L. (Miswak) Extracts against Multidrug Resistant Bacterial Clinical Isolates
title_sort antibacterial activity of salvadora persica l. (miswak) extracts against multidrug resistant bacterial clinical isolates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745819/
https://www.ncbi.nlm.nih.gov/pubmed/26904146
http://dx.doi.org/10.1155/2016/7083964
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