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Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia

Explaining how cooperation can persist in the presence of cheaters, exploiting the cooperative acts, is a challenge for evolutionary biology. Microbial systems have proved extremely useful to test evolutionary theory and identify mechanisms maintaining cooperation. One of the most widely studied sys...

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Autores principales: Sathe, Santosh, Mathew, Anugraha, Agnoli, Kirsty, Eberl, Leo, Kümmerli, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906993/
https://www.ncbi.nlm.nih.gov/pubmed/31844554
http://dx.doi.org/10.1002/evl3.144
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author Sathe, Santosh
Mathew, Anugraha
Agnoli, Kirsty
Eberl, Leo
Kümmerli, Rolf
author_facet Sathe, Santosh
Mathew, Anugraha
Agnoli, Kirsty
Eberl, Leo
Kümmerli, Rolf
author_sort Sathe, Santosh
collection PubMed
description Explaining how cooperation can persist in the presence of cheaters, exploiting the cooperative acts, is a challenge for evolutionary biology. Microbial systems have proved extremely useful to test evolutionary theory and identify mechanisms maintaining cooperation. One of the most widely studied system is the secretion and sharing of iron‐scavenging siderophores by Pseudomonas bacteria, with many insights gained from this system now being considered as hallmarks of bacterial cooperation. Here, we introduce siderophore secretion by the bacterium Burkholderia cenocepacia H111 as a novel parallel study system, and show that this system behaves differently. For ornibactin, the main siderophore of this species, we discovered a novel mechanism of how cheating can be prevented. Particularly, we found that secreted ornibactin cannot be exploited by ornibactin‐defective mutants because ornibactin receptor and synthesis genes are co‐expressed from the same operon, such that disruptive mutations in synthesis genes compromise receptor availability required for siderophore uptake and cheating. For pyochelin, the secondary siderophore of this species, we found that cheating was possible, but the relative success of cheaters was positive frequency dependent, thus diametrically opposite to the Pseudomonas and other microbial systems. Altogether, our results highlight that expanding our repertoire of microbial study systems leads to new discoveries and suggest that there is an enormous diversity of social interactions out there in nature, and we might have only looked at the tip of the iceberg so far.
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spelling pubmed-69069932019-12-16 Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia Sathe, Santosh Mathew, Anugraha Agnoli, Kirsty Eberl, Leo Kümmerli, Rolf Evol Lett Letters Explaining how cooperation can persist in the presence of cheaters, exploiting the cooperative acts, is a challenge for evolutionary biology. Microbial systems have proved extremely useful to test evolutionary theory and identify mechanisms maintaining cooperation. One of the most widely studied system is the secretion and sharing of iron‐scavenging siderophores by Pseudomonas bacteria, with many insights gained from this system now being considered as hallmarks of bacterial cooperation. Here, we introduce siderophore secretion by the bacterium Burkholderia cenocepacia H111 as a novel parallel study system, and show that this system behaves differently. For ornibactin, the main siderophore of this species, we discovered a novel mechanism of how cheating can be prevented. Particularly, we found that secreted ornibactin cannot be exploited by ornibactin‐defective mutants because ornibactin receptor and synthesis genes are co‐expressed from the same operon, such that disruptive mutations in synthesis genes compromise receptor availability required for siderophore uptake and cheating. For pyochelin, the secondary siderophore of this species, we found that cheating was possible, but the relative success of cheaters was positive frequency dependent, thus diametrically opposite to the Pseudomonas and other microbial systems. Altogether, our results highlight that expanding our repertoire of microbial study systems leads to new discoveries and suggest that there is an enormous diversity of social interactions out there in nature, and we might have only looked at the tip of the iceberg so far. John Wiley and Sons Inc. 2019-10-02 /pmc/articles/PMC6906993/ /pubmed/31844554 http://dx.doi.org/10.1002/evl3.144 Text en © 2019 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Sathe, Santosh
Mathew, Anugraha
Agnoli, Kirsty
Eberl, Leo
Kümmerli, Rolf
Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia
title Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia
title_full Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia
title_fullStr Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia
title_full_unstemmed Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia
title_short Genetic architecture constrains exploitation of siderophore cooperation in the bacterium Burkholderia cenocepacia
title_sort genetic architecture constrains exploitation of siderophore cooperation in the bacterium burkholderia cenocepacia
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906993/
https://www.ncbi.nlm.nih.gov/pubmed/31844554
http://dx.doi.org/10.1002/evl3.144
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