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Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains

Due to the indiscriminate use of antibiotics, resistance to antibiotics has increased remarkably in Staphylococcus aureus. Vancomycin is the final drug to treat the S. aureus infection, but nowadays, resistance to this antibiotic is also increasing. So, the investigation of antibiotic resistance pat...

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Autores principales: Das, Balaram, Mandal, Debasis, Dash, Sandeep Kumar, Chattopadhyay, Sourav, Tripathy, Satyajit, Dolai, Durga Pada, Dey, Sankar Kumar, Roy, Somenath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756864/
https://www.ncbi.nlm.nih.gov/pubmed/26917967
http://dx.doi.org/10.4137/IDRT.S31741
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author Das, Balaram
Mandal, Debasis
Dash, Sandeep Kumar
Chattopadhyay, Sourav
Tripathy, Satyajit
Dolai, Durga Pada
Dey, Sankar Kumar
Roy, Somenath
author_facet Das, Balaram
Mandal, Debasis
Dash, Sandeep Kumar
Chattopadhyay, Sourav
Tripathy, Satyajit
Dolai, Durga Pada
Dey, Sankar Kumar
Roy, Somenath
author_sort Das, Balaram
collection PubMed
description Due to the indiscriminate use of antibiotics, resistance to antibiotics has increased remarkably in Staphylococcus aureus. Vancomycin is the final drug to treat the S. aureus infection, but nowadays, resistance to this antibiotic is also increasing. So, the investigation of antibiotic resistance pattern is important. As there is already resistance to vancomycin, there is an urgent need to develop a new kind of antimicrobial to treat S. aureus infection. Eugenol may be the new drug of choice. This study was conducted to evaluate the antibacterial activity of eugenol against vancomycin-resistant S. aureus isolated from clinical pus samples. Thirty six pus samples were included in the study. Samples were isolated, identified and antimicrobial susceptibility tests were performed as per routine laboratory protocol. The antimicrobial activity and mechanisms of killing of eugenol were studied. Out of 36 pus samples, only 20 isolates were confirmed as S. aureus strains and 6 isolates exhibited vancomycin resistance. Eugenol successfully destroyed the vancomycin-resistant strains via reactive oxygen species generation and membrane damage. The prevalence of vancomycin resistance is increased day by day in different countries, and necessary steps to prevent the spread and emergence of resistance should be taken. The findings of the study suggested that eugenol might be used to treat vancomycin-resistant S. aureus.
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spelling pubmed-47568642016-02-25 Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains Das, Balaram Mandal, Debasis Dash, Sandeep Kumar Chattopadhyay, Sourav Tripathy, Satyajit Dolai, Durga Pada Dey, Sankar Kumar Roy, Somenath Infect Dis (Auckl) Original Research Due to the indiscriminate use of antibiotics, resistance to antibiotics has increased remarkably in Staphylococcus aureus. Vancomycin is the final drug to treat the S. aureus infection, but nowadays, resistance to this antibiotic is also increasing. So, the investigation of antibiotic resistance pattern is important. As there is already resistance to vancomycin, there is an urgent need to develop a new kind of antimicrobial to treat S. aureus infection. Eugenol may be the new drug of choice. This study was conducted to evaluate the antibacterial activity of eugenol against vancomycin-resistant S. aureus isolated from clinical pus samples. Thirty six pus samples were included in the study. Samples were isolated, identified and antimicrobial susceptibility tests were performed as per routine laboratory protocol. The antimicrobial activity and mechanisms of killing of eugenol were studied. Out of 36 pus samples, only 20 isolates were confirmed as S. aureus strains and 6 isolates exhibited vancomycin resistance. Eugenol successfully destroyed the vancomycin-resistant strains via reactive oxygen species generation and membrane damage. The prevalence of vancomycin resistance is increased day by day in different countries, and necessary steps to prevent the spread and emergence of resistance should be taken. The findings of the study suggested that eugenol might be used to treat vancomycin-resistant S. aureus. Libertas Academica 2016-02-16 /pmc/articles/PMC4756864/ /pubmed/26917967 http://dx.doi.org/10.4137/IDRT.S31741 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Original Research
Das, Balaram
Mandal, Debasis
Dash, Sandeep Kumar
Chattopadhyay, Sourav
Tripathy, Satyajit
Dolai, Durga Pada
Dey, Sankar Kumar
Roy, Somenath
Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains
title Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains
title_full Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains
title_fullStr Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains
title_full_unstemmed Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains
title_short Eugenol Provokes ROS-Mediated Membrane Damage-Associated Antibacterial Activity Against Clinically Isolated Multidrug-Resistant Staphylococcus aureus Strains
title_sort eugenol provokes ros-mediated membrane damage-associated antibacterial activity against clinically isolated multidrug-resistant staphylococcus aureus strains
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756864/
https://www.ncbi.nlm.nih.gov/pubmed/26917967
http://dx.doi.org/10.4137/IDRT.S31741
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