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Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems

Antibiotic resistance is an increasingly serious threat to global health. Consequently, the development of non-antibiotic based therapies and disinfectants, which avoid induction of resistance, or cross-resistance, is of high priority. We report the synthesis of a biocidal complex, which is produced...

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Autores principales: Tonoyan, Lilit, Fleming, Gerard T. A., Mc Cay, Paul H., Friel, Ruairi, O'Flaherty, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412088/
https://www.ncbi.nlm.nih.gov/pubmed/28512449
http://dx.doi.org/10.3389/fmicb.2017.00680
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author Tonoyan, Lilit
Fleming, Gerard T. A.
Mc Cay, Paul H.
Friel, Ruairi
O'Flaherty, Vincent
author_facet Tonoyan, Lilit
Fleming, Gerard T. A.
Mc Cay, Paul H.
Friel, Ruairi
O'Flaherty, Vincent
author_sort Tonoyan, Lilit
collection PubMed
description Antibiotic resistance is an increasingly serious threat to global health. Consequently, the development of non-antibiotic based therapies and disinfectants, which avoid induction of resistance, or cross-resistance, is of high priority. We report the synthesis of a biocidal complex, which is produced by the reaction between ionic oxidizable salts—iodide and thiocyanate—in the presence of hydrogen peroxide as an oxidation source. The reaction generates bactericidal reactive oxygen and iodine species. In this study, we report that the iodo-thiocyanate complex (ITC) is an effective bactericidal agent with activity against planktonic and biofilm cells of Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus and methicillin-resistant S. aureus) bacteria. The minimum bactericidal concentrations and the minimum biofilm eradication concentrations of the biocidal composite were in the range of 7.8–31.3 and 31.3–250 μg ml(−1), respectively. As a result, the complex was capable to cause a rapid cell death of planktonic test cultures at between 0.5 and 2 h, and complete eradication of dual and mono-species biofilms between 30 s and 10 min. Furthermore, the test bacteria, including a MRSA strain, exposed to the cocktail failed to develop resistance after serial passages. The antimicrobial activity of the ITC appears to derive from the combinational effect of the powerful species capable of oxidizing the essential biomolecules of bacteria. The use of this composition may provide an effective and efficient method for killing potential pathogens, as well as for disinfecting and removing biofilm contamination.
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spelling pubmed-54120882017-05-16 Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems Tonoyan, Lilit Fleming, Gerard T. A. Mc Cay, Paul H. Friel, Ruairi O'Flaherty, Vincent Front Microbiol Microbiology Antibiotic resistance is an increasingly serious threat to global health. Consequently, the development of non-antibiotic based therapies and disinfectants, which avoid induction of resistance, or cross-resistance, is of high priority. We report the synthesis of a biocidal complex, which is produced by the reaction between ionic oxidizable salts—iodide and thiocyanate—in the presence of hydrogen peroxide as an oxidation source. The reaction generates bactericidal reactive oxygen and iodine species. In this study, we report that the iodo-thiocyanate complex (ITC) is an effective bactericidal agent with activity against planktonic and biofilm cells of Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus and methicillin-resistant S. aureus) bacteria. The minimum bactericidal concentrations and the minimum biofilm eradication concentrations of the biocidal composite were in the range of 7.8–31.3 and 31.3–250 μg ml(−1), respectively. As a result, the complex was capable to cause a rapid cell death of planktonic test cultures at between 0.5 and 2 h, and complete eradication of dual and mono-species biofilms between 30 s and 10 min. Furthermore, the test bacteria, including a MRSA strain, exposed to the cocktail failed to develop resistance after serial passages. The antimicrobial activity of the ITC appears to derive from the combinational effect of the powerful species capable of oxidizing the essential biomolecules of bacteria. The use of this composition may provide an effective and efficient method for killing potential pathogens, as well as for disinfecting and removing biofilm contamination. Frontiers Media S.A. 2017-05-02 /pmc/articles/PMC5412088/ /pubmed/28512449 http://dx.doi.org/10.3389/fmicb.2017.00680 Text en Copyright © 2017 Tonoyan, Fleming, Mc Cay, Friel and O'Flaherty. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Tonoyan, Lilit
Fleming, Gerard T. A.
Mc Cay, Paul H.
Friel, Ruairi
O'Flaherty, Vincent
Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems
title Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems
title_full Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems
title_fullStr Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems
title_full_unstemmed Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems
title_short Antibacterial Potential of an Antimicrobial Agent Inspired by Peroxidase-Catalyzed Systems
title_sort antibacterial potential of an antimicrobial agent inspired by peroxidase-catalyzed systems
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412088/
https://www.ncbi.nlm.nih.gov/pubmed/28512449
http://dx.doi.org/10.3389/fmicb.2017.00680
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