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Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa

Iron is an essential nutrient for virtually all microbes and limiting the concentration of available iron is a potential strategy to be used as an alternative to antibiotic treatment. In this study we analysed the antimicrobial activity of two chelators, specifically 3-hydroxy-1,2-dimethyl-4(1H)-pyr...

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Autores principales: Houshmandyar, Sharareh, Eggleston, Ian M., Bolhuis, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940164/
https://www.ncbi.nlm.nih.gov/pubmed/33428087
http://dx.doi.org/10.1007/s10534-020-00281-x
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author Houshmandyar, Sharareh
Eggleston, Ian M.
Bolhuis, Albert
author_facet Houshmandyar, Sharareh
Eggleston, Ian M.
Bolhuis, Albert
author_sort Houshmandyar, Sharareh
collection PubMed
description Iron is an essential nutrient for virtually all microbes and limiting the concentration of available iron is a potential strategy to be used as an alternative to antibiotic treatment. In this study we analysed the antimicrobial activity of two chelators, specifically 3-hydroxy-1,2-dimethyl-4(1H)-pyridone (deferiprone, DFP), which is clinically approved for the treatment of iron overload disorders, and its 1,2-diethyl homologue, CP94. Both compounds showed moderate activity towards planktonically growing P. aeruginosa cells, and the mechanism of action of these chelators was indeed by limiting the amount of free iron. Surprisingly, the compounds behaved very differently when the cells were grown in biofilms. DFP also showed inhibitory effects on biofilm formation but in contrast, CP94 stimulated this process, in particular at high concentrations. We hypothesised that CP94 behaves as an iron carrier, which was confirmed by our observation that it had antimicrobial synergy with the toxic metals, gallium and copper. This suggests that P. aeruginosa produces a biofilm-specific transport protein that recognises CP94 but not the closely related compound DFP. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10534-020-00281-x.
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spelling pubmed-79401642021-03-21 Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa Houshmandyar, Sharareh Eggleston, Ian M. Bolhuis, Albert Biometals Article Iron is an essential nutrient for virtually all microbes and limiting the concentration of available iron is a potential strategy to be used as an alternative to antibiotic treatment. In this study we analysed the antimicrobial activity of two chelators, specifically 3-hydroxy-1,2-dimethyl-4(1H)-pyridone (deferiprone, DFP), which is clinically approved for the treatment of iron overload disorders, and its 1,2-diethyl homologue, CP94. Both compounds showed moderate activity towards planktonically growing P. aeruginosa cells, and the mechanism of action of these chelators was indeed by limiting the amount of free iron. Surprisingly, the compounds behaved very differently when the cells were grown in biofilms. DFP also showed inhibitory effects on biofilm formation but in contrast, CP94 stimulated this process, in particular at high concentrations. We hypothesised that CP94 behaves as an iron carrier, which was confirmed by our observation that it had antimicrobial synergy with the toxic metals, gallium and copper. This suggests that P. aeruginosa produces a biofilm-specific transport protein that recognises CP94 but not the closely related compound DFP. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10534-020-00281-x. Springer Netherlands 2021-01-11 2021 /pmc/articles/PMC7940164/ /pubmed/33428087 http://dx.doi.org/10.1007/s10534-020-00281-x Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Houshmandyar, Sharareh
Eggleston, Ian M.
Bolhuis, Albert
Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
title Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
title_full Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
title_fullStr Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
title_full_unstemmed Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
title_short Biofilm-specific uptake of a 4-pyridone-based iron chelator by Pseudomonas aeruginosa
title_sort biofilm-specific uptake of a 4-pyridone-based iron chelator by pseudomonas aeruginosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940164/
https://www.ncbi.nlm.nih.gov/pubmed/33428087
http://dx.doi.org/10.1007/s10534-020-00281-x
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