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Antibiotic stress selects against cooperation in the pathogenic bacterium Pseudomonas aeruginosa

Vasse, M., Noble, R. ORCID: 0000-0002-8057-4252, Akhmetzhanov, A. R. , Torres-Barceló, C., Gurney, J., Benateau, S., Gougat-Barbera, C., Kaltz, O. & Hochberg, M. E. (2017). Antibiotic stress selects against cooperation in the pathogenic bacterium Pseudomonas aeruginosa. Proceedings of the National Academy of Sciences of the United States of America (PNAS) ISSN 1091-6490, 114(3), pp. 546-551. doi: 10.1073/pnas.1612522114


Cheats are a pervasive threat to public goods production in natural and human communities, as they benefit from the commons without contributing to it. Although ecological antagonisms such as predation, parasitism, competition, and abiotic environmental stress play key roles in shaping population biology, it is unknown how such stresses generally affect the ability of cheats to undermine cooperation. We used theory and experiments to address this question in the pathogenic bacterium, Pseudomonas aeruginosa Although public goods producers were selected against in all populations, our competition experiments showed that antibiotics significantly increased the advantage of nonproducers. Moreover, the dominance of nonproducers in mixed cultures was associated with higher resistance to antibiotics than in either monoculture. Mathematical modeling indicates that accentuated costs to producer phenotypes underlie the observed patterns. Mathematical analysis further shows how these patterns should generalize to other taxa with public goods behaviors. Our findings suggest that explaining the maintenance of cooperative public goods behaviors in certain natural systems will be more challenging than previously thought. Our results also have specific implications for the control of pathogenic bacteria using antibiotics and for understanding natural bacterial ecosystems, where subinhibitory concentrations of antimicrobials frequently occur.

Publication Type: Article
Publisher Keywords: antibiotics; cooperation; evolution; resistance; social behavior; Anti-Bacterial Agents; Biological Evolution; Drug Resistance, Bacterial; Humans; Microbial Interactions; Models, Biological; Oligopeptides; Pseudomonas aeruginosa; Siderophores; Stress, Physiological
Subjects: Q Science > QH Natural history > QH301 Biology
R Medicine
Departments: School of Science & Technology > Mathematics
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