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Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa

Bacteria are often iron-limited, and hence produce extracellular iron-scavenging siderophores. A crucial feature of siderophore production is that it can be an altruistic behaviour (individually costly but benefitting neighbouring cells), thus siderophore producers can be invaded by non-producing so...

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Autores principales: O'Brien, Siobhán, Hodgson, David J., Buckling, Angus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071558/
https://www.ncbi.nlm.nih.gov/pubmed/24898376
http://dx.doi.org/10.1098/rspb.2014.0858
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author O'Brien, Siobhán
Hodgson, David J.
Buckling, Angus
author_facet O'Brien, Siobhán
Hodgson, David J.
Buckling, Angus
author_sort O'Brien, Siobhán
collection PubMed
description Bacteria are often iron-limited, and hence produce extracellular iron-scavenging siderophores. A crucial feature of siderophore production is that it can be an altruistic behaviour (individually costly but benefitting neighbouring cells), thus siderophore producers can be invaded by non-producing social ‘cheats’. Recent studies have shown that siderophores can also bind other heavy metals (such as Cu and Zn), but in this case siderophore chelation actually reduces metal uptake by bacteria. These complexes reduce heavy metal toxicity, hence siderophore production may contribute to toxic metal bioremediation. Here, we show that siderophore production in the context of bioremediation is also an altruistic trait and can be exploited by cheating phenotypes in the opportunistic pathogen Pseudomonas aeruginosa. Specifically, we show that in toxic copper concentrations (i) siderophore non-producers evolve de novo and reach high frequencies, and (ii) producing strains are fitter than isogenic non-producing strains in monoculture, and vice versa in co-culture. Moreover, we show that the evolutionary effect copper has on reducing siderophore production is greater than the reduction observed under iron-limited conditions. We discuss the relevance of these results to the evolution of siderophore production in natural communities and heavy metal bioremediation.
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spelling pubmed-40715582014-07-22 Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa O'Brien, Siobhán Hodgson, David J. Buckling, Angus Proc Biol Sci Research Articles Bacteria are often iron-limited, and hence produce extracellular iron-scavenging siderophores. A crucial feature of siderophore production is that it can be an altruistic behaviour (individually costly but benefitting neighbouring cells), thus siderophore producers can be invaded by non-producing social ‘cheats’. Recent studies have shown that siderophores can also bind other heavy metals (such as Cu and Zn), but in this case siderophore chelation actually reduces metal uptake by bacteria. These complexes reduce heavy metal toxicity, hence siderophore production may contribute to toxic metal bioremediation. Here, we show that siderophore production in the context of bioremediation is also an altruistic trait and can be exploited by cheating phenotypes in the opportunistic pathogen Pseudomonas aeruginosa. Specifically, we show that in toxic copper concentrations (i) siderophore non-producers evolve de novo and reach high frequencies, and (ii) producing strains are fitter than isogenic non-producing strains in monoculture, and vice versa in co-culture. Moreover, we show that the evolutionary effect copper has on reducing siderophore production is greater than the reduction observed under iron-limited conditions. We discuss the relevance of these results to the evolution of siderophore production in natural communities and heavy metal bioremediation. The Royal Society 2014-07-22 /pmc/articles/PMC4071558/ /pubmed/24898376 http://dx.doi.org/10.1098/rspb.2014.0858 Text en http://creativecommons.org/licenses/by/3.0/ © 2014 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
O'Brien, Siobhán
Hodgson, David J.
Buckling, Angus
Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa
title Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa
title_full Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa
title_fullStr Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa
title_full_unstemmed Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa
title_short Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa
title_sort social evolution of toxic metal bioremediation in pseudomonas aeruginosa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071558/
https://www.ncbi.nlm.nih.gov/pubmed/24898376
http://dx.doi.org/10.1098/rspb.2014.0858
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