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      Conflict of interest and signal interference lead to the breakdown of honest signaling

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          Abstract

          Animals use signals to coordinate a wide range of behaviors, from feeding offspring to predator avoidance. This poses an evolutionary problem, because individuals could potentially signal dishonestly to coerce others into behaving in ways that benefit the signaler. Theory suggests that honest signaling is favored when individuals share a common interest and signals carry reliable information. Here, we exploit the opportunities offered by bacterial signaling to test these predictions with an experimental evolution approach. We show that: (1) reduced relatedness leads to the relative breakdown of signaling, (2) signaling breaks down by the invasion of mutants that show both reduced signaling and reduced response to signal, (3) the genetic route to signaling breakdown is variable, and (4) the addition of artificial signal, to interfere with signal information, also leads to reduced signaling. Our results provide clear support for signaling theory, but we did not find evidence for previously predicted coercion at intermediate relatedness, suggesting that mechanistic details can alter the qualitative nature of specific predictions. Furthermore, populations evolved under low relatedness caused less mortality to insect hosts, showing how signal evolution in bacterial pathogens can drive the evolution of virulence in the opposite direction to that often predicted by theory.

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          Biological signals as handicaps.

          An ESS model of Zahavi's handicap principle is constructed. This allows a formal exposition of how the handicap principle works, and shows that its essential elements are strategic. The handicap model is about signalling, and it is proved under fairly general conditions that if the handicap principle's conditions are met, then an evolutionarily stable signalling equilibrium exists in a biological signalling system, and that any signalling equilibrium satisfies the conditions of the handicap principle. Zahavi's major claims for the handicap principle are thus vindicated. The place of cheating is discussed in view of the honesty that follows from the handicap principle. Parallel signalling models in economics are discussed. Interpretations of the handicap principle are compared. The models are not fully explicit about how females use information about male quality, and, less seriously, have no genetics. A companion paper remedies both defects in a model of the handicap principle at work in sexual selection.
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            Cooperation and conflict in quorum-sensing bacterial populations.

            It has been suggested that bacterial cells communicate by releasing and sensing small diffusible signal molecules in a process commonly known as quorum sensing (QS). It is generally assumed that QS is used to coordinate cooperative behaviours at the population level. However, evolutionary theory predicts that individuals who communicate and cooperate can be exploited. Here we examine the social evolution of QS experimentally in the opportunistic pathogen Pseudomonas aeruginosa, and show that although QS can provide a benefit at the group level, exploitative individuals can avoid the cost of producing the QS signal or of performing the cooperative behaviour that is coordinated by QS, and can therefore spread. We also show that a solution to the problem of exploitation is kin selection, if interacting bacterial cells tend to be close relatives. These results show that the problem of exploitation, which has been the focus of considerable attention in animal communication, also arises in bacteria.
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              Acyl-homoserine lactone quorum sensing: from evolution to application.

              Quorum sensing (QS) is a widespread process in bacteria that employs autoinducing chemical signals to coordinate diverse, often cooperative activities such as bioluminescence, biofilm formation, and exoenzyme secretion. Signaling via acyl-homoserine lactones is the paradigm for QS in Proteobacteria and is particularly well understood in the opportunistic pathogen Pseudomonas aeruginosa. Despite thirty years of mechanistic research, empirical studies have only recently addressed the benefits of QS and provided support for the traditional assumptions regarding its social nature and its role in optimizing cell-density-dependent group behaviors. QS-controlled public-goods production has served to investigate principles that explain the evolution and stability of cooperation, including kin selection, pleiotropic constraints, and metabolic prudence. With respect to medical application, appreciating social dynamics is pertinent to understanding the efficacy of QS-inhibiting drugs and the evolution of resistance. Future work will provide additional insight into the foundational assumptions of QS and relate laboratory discoveries to natural ecosystems.
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                Author and article information

                Contributors
                steve.diggle@nottingham.ac.uk
                Journal
                Evolution
                Evolution
                10.1111/(ISSN)1558-5646
                EVO
                Evolution; International Journal of Organic Evolution
                John Wiley and Sons Inc. (Hoboken )
                0014-3820
                1558-5646
                08 September 2015
                September 2015
                : 69
                : 9 ( doiID: 10.1111/evo.2015.69.issue-9 )
                : 2371-2383
                Affiliations
                [ 1 ] School of Life SciencesUniversity of Nottingham Nottingham NG7 2RDUnited Kingdom
                [ 2 ] Centre for Immunity, Infection and EvolutionAshworth Laboratories, University of Edinburgh King's Buildings West Mains Road Edinburgh EH9 3JTUnited Kingdom
                [ 3 ] Institute of Biological Sciences, Faculty of ScienceUniversity of Malaya 50603 Kuala LumpurMalaysia
                [ 4 ] Department of ZoologyUniversity of Oxford South Parks Road Oxford OX1 3PSUnited Kingdom
                Author notes
                [†]

                These authors are joint final author of this article.

                Article
                EVO12751
                10.1111/evo.12751
                4862024
                26282874
                f41870f5-53bf-495c-b69c-a26e074cb1d1
                © 2015 The Author(s). Evolution published by Wiley Periodicals, Inc. on behalf of The Society for the Study of Evolution.

                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.

                History
                : 19 May 2015
                : 17 July 2015
                : 27 July 2015
                Page count
                Pages: 13
                Funding
                Funded by: Royal Society, NERC
                Award ID: NE/J007064/1
                Funded by: HFSP
                Award ID: RGY0081/2012
                Funded by: The University of Malaya
                Award ID: UM.C/625/1/HIR/MOHE/CHAN/14/1, H‐50001‐A000027
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                evo12751
                September 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.1 mode:remove_FC converted:23.06.2016

                Evolutionary Biology
                population structure,selection (experimental),selection (group/kin),signaling/courtship

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