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Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus

Methicillin resistant Staphylococcus aureus (MRSA) infection is a global concern nowadays. Due to its multi-drug resistant nature, treatment with conventional antibiotics does not assure desired clinical outcomes. Therefore, there is a need to find new compounds and/or alternative methods to get ars...

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Autores principales: Kyaw, Bhone Myint, arora, Shuchi, Lim, Chu Sing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768864/
https://www.ncbi.nlm.nih.gov/pubmed/24031910
http://dx.doi.org/10.1590/S1517-838220120003000013
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author Kyaw, Bhone Myint
arora, Shuchi
Lim, Chu Sing
author_facet Kyaw, Bhone Myint
arora, Shuchi
Lim, Chu Sing
author_sort Kyaw, Bhone Myint
collection PubMed
description Methicillin resistant Staphylococcus aureus (MRSA) infection is a global concern nowadays. Due to its multi-drug resistant nature, treatment with conventional antibiotics does not assure desired clinical outcomes. Therefore, there is a need to find new compounds and/or alternative methods to get arsenal against the pathogen. Combination therapies using conventional antibiotics and phytochemicals fulfill both requirements. In this study, the efficacy of different phytochemicals in combination with selected antibiotics was tested against 12 strains of S. aureus (ATCC MRSA 43300, ATCC methicillin sensitive S. aureus or MSSA 29213 and 10 MRSA clinical strains collected from National University Hospital, Singapore). Out of the six phytochemicals used, tannic acid was synergistic with fusidic acid, minocycline, cefotaxime and rifampicin against most of strains tested and additive with ofloxacin and vancomycin. Quercetin showed synergism with minocycline, fusidic acid and rifampicin against most of the strains. Gallic acid ethyl ester showed additivity against all strains in combination with all antibiotics under investigation except with vancomycin where it showed indifference effect. Eugenol, menthone and caffeic acid showed indifference results against all strains in combination with all antibiotics. Interestingly, no antagonism was observed within these interactions. Based on the fractional inhibitory concentration indices, synergistic pairs were further examined by time-kill assays to confirm the accuracy and killing rate of the combinations over time. The two methods concurred with each other with 92% accuracy and the combinatory pairs were effective throughout the 24 hours of assay. The study suggests a possible incorporation of effective phytochemicals in combination therapies for MRSA infections.
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spelling pubmed-37688642013-09-12 Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus Kyaw, Bhone Myint arora, Shuchi Lim, Chu Sing Braz J Microbiol Medical Microbiology Methicillin resistant Staphylococcus aureus (MRSA) infection is a global concern nowadays. Due to its multi-drug resistant nature, treatment with conventional antibiotics does not assure desired clinical outcomes. Therefore, there is a need to find new compounds and/or alternative methods to get arsenal against the pathogen. Combination therapies using conventional antibiotics and phytochemicals fulfill both requirements. In this study, the efficacy of different phytochemicals in combination with selected antibiotics was tested against 12 strains of S. aureus (ATCC MRSA 43300, ATCC methicillin sensitive S. aureus or MSSA 29213 and 10 MRSA clinical strains collected from National University Hospital, Singapore). Out of the six phytochemicals used, tannic acid was synergistic with fusidic acid, minocycline, cefotaxime and rifampicin against most of strains tested and additive with ofloxacin and vancomycin. Quercetin showed synergism with minocycline, fusidic acid and rifampicin against most of the strains. Gallic acid ethyl ester showed additivity against all strains in combination with all antibiotics under investigation except with vancomycin where it showed indifference effect. Eugenol, menthone and caffeic acid showed indifference results against all strains in combination with all antibiotics. Interestingly, no antagonism was observed within these interactions. Based on the fractional inhibitory concentration indices, synergistic pairs were further examined by time-kill assays to confirm the accuracy and killing rate of the combinations over time. The two methods concurred with each other with 92% accuracy and the combinatory pairs were effective throughout the 24 hours of assay. The study suggests a possible incorporation of effective phytochemicals in combination therapies for MRSA infections. Sociedade Brasileira de Microbiologia 2012 2012-06-01 /pmc/articles/PMC3768864/ /pubmed/24031910 http://dx.doi.org/10.1590/S1517-838220120003000013 Text en © Sociedade Brasileira de Microbiologia http://creativecommons.org/licenses/by-nc/3.0/ All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License
spellingShingle Medical Microbiology
Kyaw, Bhone Myint
arora, Shuchi
Lim, Chu Sing
Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus
title Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus
title_full Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus
title_fullStr Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus
title_full_unstemmed Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus
title_short Bactericidal antibiotic-phytochemical combinations against methicillin resistant Staphylococcus aureus
title_sort bactericidal antibiotic-phytochemical combinations against methicillin resistant staphylococcus aureus
topic Medical Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768864/
https://www.ncbi.nlm.nih.gov/pubmed/24031910
http://dx.doi.org/10.1590/S1517-838220120003000013
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