FP7Reintegration grant2010–2013

PA_EXP_EVOL · Siderophore production in the human pathogen Pseudomonas aeruginosa: a model trait to study the evolution of cooperation and virulence

FP7 — People (Marie Curie Actions)

Duration
2010-07-01 → 2013-06-30
EU contribution
€45,000
Participants
1
Scheme
MC-ERG

Lines connect the coordinator with its partners.

Results in brief

Siderophore production in the human pathogen Pseudomonas aeruginosa: a model trait to study the evolution of cooperation and virulence

The occurrence of cooperation is one of the greatest challenges for evolutionary biology. The problem is why should an individual carry out a cooperative behaviour that is costly to perform, but benefits others? The evolution of such behaviour seems incompatible with the Darwinian view of competition among selfish individuals and the survival of the fittest. Despite this conundrum, cooperation is observed at all levels of biological organisation; ranging from individual cells making up a multicellular body, to social insect workers foregoing their own reproduction to help rearing the brood of their queen. Intriguingly, a great variety of cooperative traits have recently been described in microbes, such as the formation of fruiting bodies, biofilms, the communication among cells, and the release of extracellular public goods that benefit others. Because microbes are easy to handle in the laboratory they offer exciting experimental possibilities to test fundamental aspects of how natural selection can maintain and protect cooperators from the invasion of cheating mutants, which no longer contribute to but still benefit from the cooperative acts performed by others. In this project, we studied the opportunistic human pathogen Pseudomonas aeruginosa, a bacterium that secretes specific molecules (called siderophores) in the environment to scavenge essential iron for metabolism. Siderophore secretion is a cooperative trait because molecules can be shared and taken up by all individuals in the local environment. We carried out the following projects: Project#1: We examined the role of resource availability for the evolution of cooperation. In this project, we implemented relevant natural conditions into laboratory settings to better understand how multiple ecological factors jointly influence the cost and maintenance of cooperation in microbial populations. Specifically, we simulated population structure and the patchy distribution of resources as often found in natural habitats, and let bacteria evolve in these experimental habitats. We found that the propensity for cheats to arise and spread was tempered in environments that matched natural habitats more closely (i.e. increased and more patchily distributed resources). This finding helps to explain why cheating often occurs in contrived laboratory settings, but is more rarely observed under natural conditions. This study has been published in the Journal of the Evolutionary Biology (2012). Project#2: We investigated whether molecular and regulatory properties of a public good (e.g. siderophores) shape the evolution of cooperation. We showed theoretically and experimentally that extended molecular durability of public goods – allowing multiple reuse across generations – coupled to facultative regulation of the public good greatly reduced selection for cheating. This was because cooperators could facultatively reduce their investment in public goods when enough of the public good had accumulated in the media – a cost-saving strategy that minimized the ability of cheats to invade. This is the first demonstration that natural selection directly acts on the properties of a cooperative act to stabilize cooperation. This study has been published in the Proceeding of the National Academies of Sciences of the United States of America (2010). Project#3: We examined the role of public goods durability in bacterial infections. In this project, we made use of the fact that siderophores are important virulence factors in the context of acute infections. We manipulated the durability of siderophores within hosts to see how this affects virulence. Using the greater wax moth larvae (Galleria mellonella) as a host model, we found that the transition metal gallium knocks down pyoverdine during infections, which resulted in decreased bacterial growth, prolonged lifespan and increased survival rates of the host. We further found that bacteria struggle to evolve resistance against gallium, which indicates that knocking down iron-uptake pathways might be a promising, relatively evolution proof, antivirulence therapy. This study has been completed and the manuscript is soon ready for submission. Project#4: We investigated whether there is antagonistic co-evolution between cooperators and cheats. Previous work assumed that cooperators are doomed when cheats arise and consequently go extinct. In this project, we investigated whether cooperators can adapt to the presence of cheaters by becoming less exploitable, and in return, whether cheats can become more effective in cheating. To address this question, we carried out an experimental evolution study, during which we let cooperators and cheats co-evolve over prolonged periods of time. Following evolution, we sequenced evolved strains to map changes at the genetic level to behavioural performance. We found that cheat became better at cheating by turning off unnecessary metabolic pathways, and that cooperators became less vulnerable to cheating by reducing their investment into cooperation and/or by loosing the ability to disperse (i.e. they reduce mixing with cheats and thereby reduce the level of exploitation). This study provides fundamental insights into the genetic architecture of cooperative behaviours and how natural selection can act on this architecture. This study has been completed and the manuscript is about to be written up. The above-mentioned projects derived directly from the research proposed in the original grant proposal. In addition to this body of work, we have also completed and published a number of additional studies on cooperative behaviours in bacteria. Project#5: We examined why bacteria often possess multiple siderophore-based iron uptake systems for scavenging this vital resource from their environment. From an evolutionary perspective, such redundancy should not necessarily occur. We found that bacteria use a collective decision-making process to switch from producing a costly, but highly efficient siderophore, when iron is severely limited, to producing a cheaper, but less efficient siderophore, when iron is relatively more accessible. This study highlights that having multiple siderophores does not reflect redundancy, but allow bacteria to better optimize the cost-to-benefit ratio of siderophore production across changing environmental conditions. This work has been published in the Proceedings of the Royal Society of London B (2013). Project#6: We investigated the phenomenon that bacteria can commit suicide when attacked by deadly phages. This suicidal mechanism removes the phage from the population before it can propagate within the host. Importantly, we found that such altruistic suicide could be favoured by natural selection when suicide preferentially protects related clonemates from becoming infected. This work has resulted in two papers, published in the Proceedings of the Royal Society of London B (2013) and in Communicative and Integrative Biology (2013), and has received a lot of international media attention (The Scientist, Science Now, Discovery News), and has been recommended by the Faculty of 1000. More detailed information on completed and ongoing projects, as well as abstracts of all published work can be found by following these links: http://www.botinst.uzh.ch/research/evolutionary/kuemmerli/research.html http://publicationslist.org/rolf.kummerli

Data: CORDIS, © European Union

Project objective

The occurrence of cooperation is one of the greatest challenges for evolutionary biology. The problem is why should an individual carry out a cooperative behaviour that is costly to perform, but benefits other individuals? The theoretical framework of inclusive fitness has proofed extremely successful in explaining the evolution of cooperation across a wide number of taxa ranging from microbes to mammals. Particularly, the investigation of microbial cooperative systems have opened a completely new research area because microbes allow observing the evolution of cooperation in real-time. Furthermore, many cooperative traits are involved with virulence in infections of humans, and have therefore medical relevance. Consequently, the research in this area is highly interdisciplinary connecting the fields of evolutionary biology, microbiology and medicine. This proposal focuses on the production of siderophore molecules in the opportunistic human pathogen Pseudomonas aeruginosa. Iron is a major limiting factor for bacterial growth and in response to iron deficiency, P. aeruginosa releases siderophore molecules into the local environment to scavenge insoluble iron, making it available for bacterial metabolism. Siderophore production is a cooperative behaviour as it can provide a fitness benefit to neighbouring cells, which can take up iron bound to siderophore produced by others. This proposal uses cooperative siderophore production to study: (i) the properties of siderophore molecules as a cooperative good and virulence factor, and assess the fitness consequences for cooperative wildtype and non-cooperative mutant strains in mixed cultures in vitro and in animal host models; (ii) the dynamics of cooperative and non-cooperative strains under different environmental conditions as they may occur in nature; and (iii) the adaptive responses of cooperators to the presence of non-cooperative strains at the behavioural and genetic level in an experimental evolution set up.

Original text from CORDIS.

Participants

  • EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH · ZuerichCoordinatorSwitzerland

Links

Data: CORDIS, © European Union