ArticleBMC evolutionary biology2016
Ecological conditions determine extinction risk in co-evolving bacteria-phage populations.
Article in BMC evolutionary biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Article
- Factors Affecting Phage-Bacteria Coevolution Dynamics.Viruses · 2025Review
- Nutrient-rich spatial refuges buffer against extinction and promote evolutionary rescue in evolving microbial populations.Proceedings. Biological sciences · 2024Article
- Trade-offs between receptor modification and fitness drive host-bacteriophage co-evolution leading to phage extinction or co-existence.The ISME journal · 2024Article
- Phage-encoded depolymerases as a strategy for combating multidrug-resistantFrontiers in cellular and infection microbiology · 2024Review
- Coevolutionary theory of hosts and parasites.Journal of evolutionary biology · 2022Review
- Ecology directs host-parasite coevolutionary trajectories across Daphnia-microparasite populations.Nature ecology & evolution · 2021Article
- The evolution of host resistance and parasite infectivity is highest in seasonal resource environments that oscillate at intermediate amplitudes.Proceedings. Biological sciences · 2020Article
- Trends of Microdiversity Reveal Depth-Dependent Evolutionary Strategies of Viruses in the Mediterranean.mSystems · 2019Article
- Conflicting selection alters the trajectory of molecular evolution in a tripartite bacteria-plasmid-phage interaction.Molecular ecology · 2017Article
- Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAntagonistic coevolution between bacteria and their viral parasites, phage, drives continual evolution of resistance and infectivity traits through recurrent cycles of adaptation and counter-adaptation. Both partners are vulnerable to extinction through failure of adaptation. Environmental conditions may impose unequal abiotic selection pressures on each partner, destabilising the coevolutionary relationship and increasing the extinction risk of one partner. In this study we explore how the degree of population mixing and resource supply affect coevolution-induced extinction risk by coevolving replicate populations of Pseudomonas fluorescens SBW25 with its associated lytic phage SBW25Ф2 under four treatment regimens incorporating low and high resource availability with mixed or static growth conditions.
resultsWe observed an increased risk of phage extinction under population mixing, and in low resource conditions. High levels of evolved bacterial resistance promoted phage extinction at low resources under both mixed and static conditions, whereas phage populations could survive when phage susceptible bacterial genotypes rose to high frequency.
conclusionsThese findings demonstrate that phage extinction risk is influenced by multiple abiotic conditions, which together act to destabilise the bacteria-phage coevolutionary relationship. The risk of coevolution-induced extinction is therefore dependent on the ecological context.
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