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Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin

Antimicrobial resistance is a growing global concern in human and veterinary medicine, with an ever-increasing void in the arsenal of clinicians. Novel classes of compounds including carbon monoxoide-releasing molecules (CORMs), for example the light-activated metal complex [Mn(CO)(3)(tpa-κ(3)N)]Br,...

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Autores principales: Betts, Jonathan, Nagel, Christopher, Schatzschneider, Ulrich, Poole, Robert, La Ragione, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645124/
https://www.ncbi.nlm.nih.gov/pubmed/29040287
http://dx.doi.org/10.1371/journal.pone.0186359
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author Betts, Jonathan
Nagel, Christopher
Schatzschneider, Ulrich
Poole, Robert
La Ragione, Robert M.
author_facet Betts, Jonathan
Nagel, Christopher
Schatzschneider, Ulrich
Poole, Robert
La Ragione, Robert M.
author_sort Betts, Jonathan
collection PubMed
description Antimicrobial resistance is a growing global concern in human and veterinary medicine, with an ever-increasing void in the arsenal of clinicians. Novel classes of compounds including carbon monoxoide-releasing molecules (CORMs), for example the light-activated metal complex [Mn(CO)(3)(tpa-κ(3)N)]Br, could be used as alternatives/to supplement traditional antibacterials. Avian pathogenic Escherichia coli (APEC) represent a large reservoir of antibiotic resistance and can cause serious clinical disease in poultry, with potential as zoonotic pathogens, due to shared serotypes and virulence factors with human pathogenic E. coli. The in vitro activity of [Mn(CO)(3)(tpa-κ(3)N)]Br against multidrug-resistant APECs was assessed via broth microtitre dilution assays and synergy testing with colistin performed using checkerboard and time-kill assays. In vivo antibacterial activity of [Mn(CO)(3)(tpa-κ(3)N)]Br alone and in combination with colistin was determined using the Galleria mellonella wax moth larvae model. Animals were monitored for life/death, melanisation and bacterial numbers enumerated from larval haemolymph. In vitro testing produced relatively high [Mn(CO)(3)(tpa-κ(3)N)]Br minimum inhibitory concentrations (MICs) of 1024 mg/L. However, its activity was significantly increased with the addition of colistin, bringing MICs down to ≤32 mg/L. This synergy was confirmed in time-kill assays. In vivo assays showed that the combination of [Mn(CO)(3)(tpa-κ(3)N)]Br with colistin produced superior bacterial killing and significantly increased larval survival. In both in vitro and in vivo assays light activation was not required for antibacterial activity. This data supports further evaluation of [Mn(CO)(3)(tpa-κ(3)N)]Br as a potential agent for treatment of systemic infections in humans and animals, when used with permeabilising agents such as colistin.
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spelling pubmed-56451242017-10-30 Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin Betts, Jonathan Nagel, Christopher Schatzschneider, Ulrich Poole, Robert La Ragione, Robert M. PLoS One Research Article Antimicrobial resistance is a growing global concern in human and veterinary medicine, with an ever-increasing void in the arsenal of clinicians. Novel classes of compounds including carbon monoxoide-releasing molecules (CORMs), for example the light-activated metal complex [Mn(CO)(3)(tpa-κ(3)N)]Br, could be used as alternatives/to supplement traditional antibacterials. Avian pathogenic Escherichia coli (APEC) represent a large reservoir of antibiotic resistance and can cause serious clinical disease in poultry, with potential as zoonotic pathogens, due to shared serotypes and virulence factors with human pathogenic E. coli. The in vitro activity of [Mn(CO)(3)(tpa-κ(3)N)]Br against multidrug-resistant APECs was assessed via broth microtitre dilution assays and synergy testing with colistin performed using checkerboard and time-kill assays. In vivo antibacterial activity of [Mn(CO)(3)(tpa-κ(3)N)]Br alone and in combination with colistin was determined using the Galleria mellonella wax moth larvae model. Animals were monitored for life/death, melanisation and bacterial numbers enumerated from larval haemolymph. In vitro testing produced relatively high [Mn(CO)(3)(tpa-κ(3)N)]Br minimum inhibitory concentrations (MICs) of 1024 mg/L. However, its activity was significantly increased with the addition of colistin, bringing MICs down to ≤32 mg/L. This synergy was confirmed in time-kill assays. In vivo assays showed that the combination of [Mn(CO)(3)(tpa-κ(3)N)]Br with colistin produced superior bacterial killing and significantly increased larval survival. In both in vitro and in vivo assays light activation was not required for antibacterial activity. This data supports further evaluation of [Mn(CO)(3)(tpa-κ(3)N)]Br as a potential agent for treatment of systemic infections in humans and animals, when used with permeabilising agents such as colistin. Public Library of Science 2017-10-17 /pmc/articles/PMC5645124/ /pubmed/29040287 http://dx.doi.org/10.1371/journal.pone.0186359 Text en © 2017 Betts et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Betts, Jonathan
Nagel, Christopher
Schatzschneider, Ulrich
Poole, Robert
La Ragione, Robert M.
Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin
title Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin
title_full Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin
title_fullStr Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin
title_full_unstemmed Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin
title_short Antimicrobial activity of carbon monoxide-releasing molecule [Mn(CO)(3)(tpa-κ(3)N)]Br versus multidrug-resistant isolates of Avian Pathogenic Escherichia coli and its synergy with colistin
title_sort antimicrobial activity of carbon monoxide-releasing molecule [mn(co)(3)(tpa-κ(3)n)]br versus multidrug-resistant isolates of avian pathogenic escherichia coli and its synergy with colistin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645124/
https://www.ncbi.nlm.nih.gov/pubmed/29040287
http://dx.doi.org/10.1371/journal.pone.0186359
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