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

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          Abstract

          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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          Most cited references55

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          Siderophore-based iron acquisition and pathogen control.

          High-affinity iron acquisition is mediated by siderophore-dependent pathways in the majority of pathogenic and nonpathogenic bacteria and fungi. Considerable progress has been made in characterizing and understanding mechanisms of siderophore synthesis, secretion, iron scavenging, and siderophore-delivered iron uptake and its release. The regulation of siderophore pathways reveals multilayer networks at the transcriptional and posttranscriptional levels. Due to the key role of many siderophores during virulence, coevolution led to sophisticated strategies of siderophore neutralization by mammals and (re)utilization by bacterial pathogens. Surprisingly, hosts also developed essential siderophore-based iron delivery and cell conversion pathways, which are of interest for diagnostic and therapeutic studies. In the last decades, natural and synthetic compounds have gained attention as potential therapeutics for iron-dependent treatment of infections and further diseases. Promising results for pathogen inhibition were obtained with various siderophore-antibiotic conjugates acting as "Trojan horse" toxins and siderophore pathway inhibitors. In this article, general aspects of siderophore-mediated iron acquisition, recent findings regarding iron-related pathogen-host interactions, and current strategies for iron-dependent pathogen control will be reviewed. Further concepts including the inhibition of novel siderophore pathway targets are discussed.
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            Chemistry and biology of siderophores.

            Siderophores are compounds produced by bacteria, fungi and graminaceous plants for scavenging iron from the environment. They are low-molecular-weight compounds (500-1500 daltons) possessing a high affinity for iron(III) (Kf > 1030), the biosynthesis of which is regulated by iron levels and the function of which is to supply iron to the cell. This article briefly describes the classification and chemical properties of siderophores, before outlining research on siderophore biosynthesis and transport. Clinically important siderophores and the therapeutic potential of siderophore design are described. Appendix 1 provides a comprehensive list of siderophore structures.
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              Social evolution theory for microorganisms.

              Microorganisms communicate and cooperate to perform a wide range of multicellular behaviours, such as dispersal, nutrient acquisition, biofilm formation and quorum sensing. Microbiologists are rapidly gaining a greater understanding of the molecular mechanisms involved in these behaviours, and the underlying genetic regulation. Such behaviours are also interesting from the perspective of social evolution - why do microorganisms engage in these behaviours given that cooperative individuals can be exploited by selfish cheaters, who gain the benefit of cooperation without paying their share of the cost? There is great potential for interdisciplinary research in this fledgling field of sociomicrobiology, but a limiting factor is the lack of effective communication of social evolution theory to microbiologists. Here, we provide a conceptual overview of the different mechanisms through which cooperative behaviours can be stabilized, emphasizing the aspects most relevant to microorganisms, the novel problems that microorganisms pose and the new insights that can be gained from applying evolutionary theory to microorganisms.
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                Author and article information

                Contributors
                santosh.iisc@gmail.com
                rolf.kuemmerli@uzh.ch
                Journal
                Evol Lett
                Evol Lett
                10.1002/(ISSN)2056-3744
                EVL3
                Evolution Letters
                John Wiley and Sons Inc. (Hoboken )
                2056-3744
                02 October 2019
                December 2019
                : 3
                : 6 ( doiID: 10.1002/evl3.v3.6 )
                : 610-622
                Affiliations
                [ 1 ] Department of Plant and Microbial Biology University of Zürich Zürich Switzerland
                [ 2 ] Department of Quantitative Biomedicine University of Zürich Zürich Switzerland
                Author information
                https://orcid.org/0000-0002-4952-1443
                https://orcid.org/0000-0002-2058-8783
                https://orcid.org/0000-0002-6317-1996
                https://orcid.org/0000-0002-7241-0864
                https://orcid.org/0000-0003-4084-6679
                Article
                EVL3144
                10.1002/evl3.144
                6906993
                31844554
                211a7c7e-d194-4748-ad2c-7c7991dafc6c
                © 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.

                History
                : 09 April 2019
                : 28 August 2019
                : 03 September 2019
                Page count
                Figures: 5, Tables: 0, Pages: 13, Words: 8820
                Funding
                Funded by: Swiss National Science Foundation , open-funder-registry 10.13039/501100001711;
                Award ID: 31003A_169307
                Award ID: PP00P3_165835
                Funded by: European Research Council , open-funder-registry 10.13039/501100000781;
                Award ID: grant agreement n° 681295
                Categories
                Letter
                Letters
                Custom metadata
                2.0
                December 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:12.12.2019

                cheating,pleiotropy,genetic architecture,microbial cooperation,public goods,siderophores

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