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Positive selection and compensatory adaptation interact to stabilize non-transmissible plasmids

Author

Listed:
  • A. San Millan

    (University of Oxford)

  • R. Peña-Miller

    (University of Oxford
    Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México)

  • M. Toll-Riera

    (University of Oxford)

  • Z. V. Halbert

    (University of Oxford)

  • A. R. McLean

    (University of Oxford)

  • B. S. Cooper

    (Centre for Tropical Medicine, University of Oxford
    Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University)

  • R. C. MacLean

    (University of Oxford)

Abstract

Plasmids are important drivers of bacterial evolution, but it is challenging to understand how plasmids persist over the long term because plasmid carriage is costly. Classical models predict that horizontal transfer is necessary for plasmid persistence, but recent work shows that almost half of plasmids are non-transmissible. Here we use a combination of mathematical modelling and experimental evolution to investigate how a costly, non-transmissible plasmid, pNUK73, can be maintained in populations of Pseudomonas aeruginosa. Compensatory adaptation increases plasmid stability by eliminating the cost of plasmid carriage. However, positive selection for plasmid-encoded antibiotic resistance is required to maintain the plasmid by offsetting reductions in plasmid frequency due to segregational loss. Crucially, we show that compensatory adaptation and positive selection reinforce each other’s effects. Our study provides a new understanding of how plasmids persist in bacterial populations, and it helps to explain why resistance can be maintained after antibiotic use is stopped.

Suggested Citation

  • A. San Millan & R. Peña-Miller & M. Toll-Riera & Z. V. Halbert & A. R. McLean & B. S. Cooper & R. C. MacLean, 2014. "Positive selection and compensatory adaptation interact to stabilize non-transmissible plasmids," Nature Communications, Nature, vol. 5(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6208
    DOI: 10.1038/ncomms6208
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    Cited by:

    1. Julio Diaz Caballero & Rachel M. Wheatley & Natalia Kapel & Carla López-Causapé & Thomas Van der Schalk & Angus Quinn & Liam P. Shaw & Lois Ogunlana & Claudia Recanatini & Basil Britto Xavier & Leen T, 2023. "Mixed strain pathogen populations accelerate the evolution of antibiotic resistance in patients," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Olesia Werbowy & Sławomir Werbowy & Tadeusz Kaczorowski, 2017. "Plasmid stability analysis based on a new theoretical model employing stochastic simulations," PLOS ONE, Public Library of Science, vol. 12(8), pages 1-21, August.
    3. J. Carlos R. Hernandez-Beltran & Jerónimo Rodríguez-Beltrán & Oscar Bruno Aguilar-Luviano & Jesús Velez-Santiago & Octavio Mondragón-Palomino & R. Craig MacLean & Ayari Fuentes-Hernández & Alvaro San , 2024. "Plasmid-mediated phenotypic noise leads to transient antibiotic resistance in bacteria," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    4. Rachel M. Wheatley & Julio Diaz Caballero & Thomas E. Schalk & Fien H. R. Winter & Liam P. Shaw & Natalia Kapel & Claudia Recanatini & Leen Timbermont & Jan Kluytmans & Mark Esser & Alicia Lacoma & Cr, 2022. "Gut to lung translocation and antibiotic mediated selection shape the dynamics of Pseudomonas aeruginosa in an ICU patient," Nature Communications, Nature, vol. 13(1), pages 1-11, December.

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