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Unsuspected pyocyanin effect in yeast under anaerobiosis

The blue–green phenazine, Pyocyanin (PYO), is a well-known virulence factor produced by Pseudomonas aeruginosa, notably during cystic fibrosis lung infections. It is toxic to both eukaryotic and bacterial cells and several mechanisms, including the induction of oxidative stress, have been postulated...

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Autores principales: Barakat, Rana, Goubet, Isabelle, Manon, Stephen, Berges, Thierry, Rosenfeld, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937724/
https://www.ncbi.nlm.nih.gov/pubmed/24307284
http://dx.doi.org/10.1002/mbo3.142
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author Barakat, Rana
Goubet, Isabelle
Manon, Stephen
Berges, Thierry
Rosenfeld, Eric
author_facet Barakat, Rana
Goubet, Isabelle
Manon, Stephen
Berges, Thierry
Rosenfeld, Eric
author_sort Barakat, Rana
collection PubMed
description The blue–green phenazine, Pyocyanin (PYO), is a well-known virulence factor produced by Pseudomonas aeruginosa, notably during cystic fibrosis lung infections. It is toxic to both eukaryotic and bacterial cells and several mechanisms, including the induction of oxidative stress, have been postulated. However, the mechanism of PYO toxicity under the physiological conditions of oxygen limitation that are encountered by P. aeruginosa and by target organisms in vivo remains unclear. In this study, wild-type and mutant strains of the yeast Saccharomyces cerevisiae were used as an effective eukaryotic model to determine the toxicity of PYO (100–500 μmol/L) under key growth conditions. Under respiro-fermentative conditions (with glucose as substrate), WT strains and certain H(2)O(2)-hypersensitive strains showed a low-toxic response to PYO. Under respiratory conditions (with glycerol as substrate) all the strains tested were significantly more sensitive to PYO. Four antioxidants were tested but only N-acetylcysteine was capable of partially counteracting PYO toxicity. PYO did not appear to affect short-term respiratory O(2) uptake, but it did seem to interfere with cyanide-poisoned mitochondria through a complex III-dependent mechanism. Therefore, a combination of oxidative stress and respiration disturbance could partly explain aerobic PYO toxicity. Surprisingly, the toxic effects of PYO were more significant under anaerobic conditions. More pronounced effects were observed in several strains including a ‘petite’ strain lacking mitochondrial DNA, strains with increased or decreased levels of ABC transporters, and strains deficient in DNA damage repair. Therefore, even though PYO is toxic for actively respiring cells, O(2) may indirectly protect the cells from the higher anaerobic-linked toxicity of PYO. The increased sensitivity to PYO under anaerobic conditions is not unique to S. cerevisiae and was also observed in another yeast, Candida albicans.
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spelling pubmed-39377242014-03-07 Unsuspected pyocyanin effect in yeast under anaerobiosis Barakat, Rana Goubet, Isabelle Manon, Stephen Berges, Thierry Rosenfeld, Eric Microbiologyopen Original Research The blue–green phenazine, Pyocyanin (PYO), is a well-known virulence factor produced by Pseudomonas aeruginosa, notably during cystic fibrosis lung infections. It is toxic to both eukaryotic and bacterial cells and several mechanisms, including the induction of oxidative stress, have been postulated. However, the mechanism of PYO toxicity under the physiological conditions of oxygen limitation that are encountered by P. aeruginosa and by target organisms in vivo remains unclear. In this study, wild-type and mutant strains of the yeast Saccharomyces cerevisiae were used as an effective eukaryotic model to determine the toxicity of PYO (100–500 μmol/L) under key growth conditions. Under respiro-fermentative conditions (with glucose as substrate), WT strains and certain H(2)O(2)-hypersensitive strains showed a low-toxic response to PYO. Under respiratory conditions (with glycerol as substrate) all the strains tested were significantly more sensitive to PYO. Four antioxidants were tested but only N-acetylcysteine was capable of partially counteracting PYO toxicity. PYO did not appear to affect short-term respiratory O(2) uptake, but it did seem to interfere with cyanide-poisoned mitochondria through a complex III-dependent mechanism. Therefore, a combination of oxidative stress and respiration disturbance could partly explain aerobic PYO toxicity. Surprisingly, the toxic effects of PYO were more significant under anaerobic conditions. More pronounced effects were observed in several strains including a ‘petite’ strain lacking mitochondrial DNA, strains with increased or decreased levels of ABC transporters, and strains deficient in DNA damage repair. Therefore, even though PYO is toxic for actively respiring cells, O(2) may indirectly protect the cells from the higher anaerobic-linked toxicity of PYO. The increased sensitivity to PYO under anaerobic conditions is not unique to S. cerevisiae and was also observed in another yeast, Candida albicans. John Wiley & Sons Ltd 2014-02 2013-12-05 /pmc/articles/PMC3937724/ /pubmed/24307284 http://dx.doi.org/10.1002/mbo3.142 Text en © 2013 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Barakat, Rana
Goubet, Isabelle
Manon, Stephen
Berges, Thierry
Rosenfeld, Eric
Unsuspected pyocyanin effect in yeast under anaerobiosis
title Unsuspected pyocyanin effect in yeast under anaerobiosis
title_full Unsuspected pyocyanin effect in yeast under anaerobiosis
title_fullStr Unsuspected pyocyanin effect in yeast under anaerobiosis
title_full_unstemmed Unsuspected pyocyanin effect in yeast under anaerobiosis
title_short Unsuspected pyocyanin effect in yeast under anaerobiosis
title_sort unsuspected pyocyanin effect in yeast under anaerobiosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937724/
https://www.ncbi.nlm.nih.gov/pubmed/24307284
http://dx.doi.org/10.1002/mbo3.142
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