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Coevolution with viruses drives the evolution of bacterial mutation rates

Author

Listed:
  • Csaba Pal

    (University of Oxford
    Institute of Biochemistry, Biological Research Center, Temesvári krt. 62. Szeged, H-6701, Hungary)

  • María D. Maciá

    (Servicio de Microbiologia and Unidad de Investigación, Hospital Son Dureta, Instituto Universitario de Investigación en Ciencias de la Salud (IUNICS), 07014, Palma de Mallorca, Spain)

  • Antonio Oliver

    (Servicio de Microbiologia and Unidad de Investigación, Hospital Son Dureta, Instituto Universitario de Investigación en Ciencias de la Salud (IUNICS), 07014, Palma de Mallorca, Spain)

  • Ira Schachar

    (University of Oxford)

  • Angus Buckling

    (University of Oxford)

Abstract

Driven by competition Bacterial cultures in changing environments sometimes accumulate 'mutator' strains, with elevated mutation rates, presumably to enhance their potential for adaptive evolution. This can often happen in clinical situations. If they are to persist, mutators need a consistently changing environment. Coevolution with parasites, such as viruses, is a scenario that can provide that. Experiments with Pseudomonas fluorescens now show that coevolution with a naturally occurring bacteriophage significantly increases bacterial mutation rates — and results in a higher probability of phage extinction. Targeting phage populations might therefore be a way of weakening selection for mutator bacteria in clinical infections.

Suggested Citation

  • Csaba Pal & María D. Maciá & Antonio Oliver & Ira Schachar & Angus Buckling, 2007. "Coevolution with viruses drives the evolution of bacterial mutation rates," Nature, Nature, vol. 450(7172), pages 1079-1081, December.
  • Handle: RePEc:nat:nature:v:450:y:2007:i:7172:d:10.1038_nature06350
    DOI: 10.1038/nature06350
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    Cited by:

    1. Liberman, Uri & Behar, Hilla & Feldman, Marcus W., 2016. "Evolution of reduced mutation under frequency-dependent selection," Theoretical Population Biology, Elsevier, vol. 112(C), pages 52-59.
    2. Antun Skanata & Edo Kussell, 2021. "Ecological memory preserves phage resistance mechanisms in bacteria," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
    3. Greenspoon, Philip B. & Mideo, Nicole, 2017. "Evolutionary rescue of a parasite population by mutation rate evolution," Theoretical Population Biology, Elsevier, vol. 117(C), pages 64-75.
    4. Baumdicker, Franz & Sester-Huss, Elisabeth & Pfaffelhuber, Peter, 2020. "Modifiers of mutation rate in selectively fluctuating environments," Stochastic Processes and their Applications, Elsevier, vol. 130(11), pages 6843-6862.
    5. M’Gonigle, L.K. & Shen, J.J. & Otto, S.P., 2009. "Mutating away from your enemies: The evolution of mutation rate in a host–parasite system," Theoretical Population Biology, Elsevier, vol. 75(4), pages 301-311.

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