IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1009417.html
   My bibliography  Save this article

Phenotypic-dependent variability and the emergence of tolerance in bacterial populations

Author

Listed:
  • José Camacho Mateu
  • Matteo Sireci
  • Miguel A Muñoz

Abstract

Ecological and evolutionary dynamics have been historically regarded as unfolding at broadly separated timescales. However, these two types of processes are nowadays well-documented to intersperse much more tightly than traditionally assumed, especially in communities of microorganisms. Advancing the development of mathematical and computational approaches to shed novel light onto eco-evolutionary problems is a challenge of utmost relevance. With this motivation in mind, here we scrutinize recent experimental results showing evidence of rapid evolution of tolerance by lag in bacterial populations that are periodically exposed to antibiotic stress in laboratory conditions. In particular, the distribution of single-cell lag times—i.e., the times that individual bacteria from the community remain in a dormant state to cope with stress—evolves its average value to approximately fit the antibiotic-exposure time. Moreover, the distribution develops right-skewed heavy tails, revealing the presence of individuals with anomalously large lag times. Here, we develop a parsimonious individual-based model mimicking the actual demographic processes of the experimental setup. Individuals are characterized by a single phenotypic trait: their intrinsic lag time, which is transmitted with variation to the progeny. The model—in a version in which the amplitude of phenotypic variations grows with the parent’s lag time—is able to reproduce quite well the key empirical observations. Furthermore, we develop a general mathematical framework allowing us to describe with good accuracy the properties of the stochastic model by means of a macroscopic equation, which generalizes the Crow-Kimura equation in population genetics. Even if the model does not account for all the biological mechanisms (e.g., genetic changes) in a detailed way—i.e., it is a phenomenological one—it sheds light onto the eco-evolutionary dynamics of the problem and can be helpful to design strategies to hinder the emergence of tolerance in bacterial communities. From a broader perspective, this work represents a benchmark for the mathematical framework designed to tackle much more general eco-evolutionary problems, thus paving the road to further research avenues.Author summary: Problems in which ecological and evolutionary changes occur at similar timescales and feedback into each other are ubiquitous and of outmost importance, especially in microbiology. A particularly relevant problem is that of the emergence of tolerance to antibiotics by lag, that has been recently shown to emerge very fast in bacterial (E. coli) populations under controlled laboratory conditions. Here, we present a computational individual-based model, allowing us to reproduce empirical observations and, also, introduce a very general analytical framework to rationalize such results. We believe that our combined computational and analytical approach may inform the development of well-informed strategies to mitigate the emergence of bacterial tolerance and resistance to antibiotics and, more generally, can help shedding light onto more general eco-evolutionary problems.

Suggested Citation

  • José Camacho Mateu & Matteo Sireci & Miguel A Muñoz, 2021. "Phenotypic-dependent variability and the emergence of tolerance in bacterial populations," PLOS Computational Biology, Public Library of Science, vol. 17(9), pages 1-28, September.
  • Handle: RePEc:plo:pcbi00:1009417
    DOI: 10.1371/journal.pcbi.1009417
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1009417
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1009417&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1009417?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. U. Dieckmann & M. Doebeli, 1999. "On the Origin of Species by Sympatric Speciation," Working Papers ir99013, International Institute for Applied Systems Analysis.
    2. U. Dieckmann & R. Law, 1996. "The Dynamical Theory of Coevolution: A Derivation from Stochastic Ecological Processes," Working Papers wp96001, International Institute for Applied Systems Analysis.
    3. Yusuke Himeoka & Namiko Mitarai, 2021. "When to wake up? The optimal waking-up strategies for starvation-induced persistence," PLOS Computational Biology, Public Library of Science, vol. 17(2), pages 1-21, February.
    4. Gil Jorge Barros Henriques & Koichi Ito & Christoph Hauert & Michael Doebeli, 2021. "On the importance of evolving phenotype distributions on evolutionary diversification," PLOS Computational Biology, Public Library of Science, vol. 17(2), pages 1-21, February.
    5. Ulf Dieckmann & Michael Doebeli, 1999. "On the origin of species by sympatric speciation," Nature, Nature, vol. 400(6742), pages 354-357, July.
    6. Ofer Fridman & Amir Goldberg & Irine Ronin & Noam Shoresh & Nathalie Q. Balaban, 2014. "Optimization of lag time underlies antibiotic tolerance in evolved bacterial populations," Nature, Nature, vol. 513(7518), pages 418-421, September.
    7. M. Doebeli & U. Dieckmann, 2000. "Evolutionary Branching and Sympatric Speciation Caused by Different Types of Ecological Interactions," Working Papers ir00040, International Institute for Applied Systems Analysis.
    8. Erik S. Barton & Douglas W. White & Jason S. Cathelyn & Kelly A. Brett-McClellan & Michael Engle & Michael S. Diamond & Virginia L. Miller & Herbert W. Virgin, 2007. "Herpesvirus latency confers symbiotic protection from bacterial infection," Nature, Nature, vol. 447(7142), pages 326-329, May.
    9. Michael Doebeli & Ulf Dieckmann, 2003. "Speciation along environmental gradients," Nature, Nature, vol. 421(6920), pages 259-264, January.
    10. Alper Mutlu & Stephanie Trauth & Marika Ziesack & Katja Nagler & Jan-Philip Bergeest & Karl Rohr & Nils Becker & Thomas Höfer & Ilka B. Bischofs, 2018. "Phenotypic memory in Bacillus subtilis links dormancy entry and exit by a spore quantity-quality tradeoff," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Åke Brännström & Jacob Johansson & Niels Von Festenberg, 2013. "The Hitchhiker’s Guide to Adaptive Dynamics," Games, MDPI, vol. 4(3), pages 1-25, June.
    2. Troost, T.A. & Kooi, B.W. & Kooijman, S.A.L.M., 2007. "Bifurcation analysis of ecological and evolutionary processes in ecosystems," Ecological Modelling, Elsevier, vol. 204(1), pages 253-268.
    3. Zu, Jian & Wang, Jinliang, 2013. "Adaptive evolution of attack ability promotes the evolutionary branching of predator species," Theoretical Population Biology, Elsevier, vol. 89(C), pages 12-23.
    4. Nurmi, Tuomas & Parvinen, Kalle, 2008. "On the evolution of specialization with a mechanistic underpinning in structured metapopulations," Theoretical Population Biology, Elsevier, vol. 73(2), pages 222-243.
    5. Débarre, Florence & Otto, Sarah P., 2016. "Evolutionary dynamics of a quantitative trait in a finite asexual population," Theoretical Population Biology, Elsevier, vol. 108(C), pages 75-88.
    6. Boettiger, Carl & Dushoff, Jonathan & Weitz, Joshua S., 2010. "Fluctuation domains in adaptive evolution," Theoretical Population Biology, Elsevier, vol. 77(1), pages 6-13.
    7. Svardal, Hannes & Rueffler, Claus & Hermisson, Joachim, 2015. "A general condition for adaptive genetic polymorphism in temporally and spatially heterogeneous environments," Theoretical Population Biology, Elsevier, vol. 99(C), pages 76-97.
    8. Champagnat, Nicolas, 2006. "A microscopic interpretation for adaptive dynamics trait substitution sequence models," Stochastic Processes and their Applications, Elsevier, vol. 116(8), pages 1127-1160, August.
    9. E. Kisdi & F.J.A. Jacobs & S.A.H. Geritz, 2000. "Red Queen Evolution by Cycles of Evolutionary Branching and Extinction," Working Papers ir00030, International Institute for Applied Systems Analysis.
    10. Matessi, Carlo & Schneider, Kristan A., 2009. "Optimization under frequency-dependent selection," Theoretical Population Biology, Elsevier, vol. 76(1), pages 1-12.
    11. Bagnoli, Franco & Guardiani, Carlo, 2005. "A model of sympatric speciation through assortative mating," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 347(C), pages 534-574.
    12. Bhattacharyay, A. & Drossel, B., 2005. "Modeling coevolution and sympatric speciation of flowers and pollinators," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 345(1), pages 159-172.
    13. Sakamoto, T. & Innan, H., 2020. "Establishment process of a magic trait allele subject to both divergent selection and assortative mating," Theoretical Population Biology, Elsevier, vol. 135(C), pages 9-18.
    14. Cook, James N. & Oono, Y., 2010. "Competitive localization," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 389(9), pages 1849-1860.
    15. Rettelbach, Agnes & Hermisson, Joachim & Dieckmann, Ulf & Kopp, Michael, 2011. "Effects of genetic architecture on the evolution of assortative mating under frequency-dependent disruptive selection," Theoretical Population Biology, Elsevier, vol. 79(3), pages 82-96.
    16. Jonathan Newton, 2017. "The preferences of Homo Moralis are unstable under evolving assortativity," International Journal of Game Theory, Springer;Game Theory Society, vol. 46(2), pages 583-589, May.
    17. Cressman, Ross & Hofbauer, Josef & Riedel, Frank, 2005. "Stability of the Replicator Equation for a Single-Species with a Multi-Dimensional Continuous Trait Space," Bonn Econ Discussion Papers 12/2005, University of Bonn, Bonn Graduate School of Economics (BGSE).
    18. Alexandros Rigos & Heinrich H. Nax, 2015. "Assortativity evolving from social dilemmas," Discussion Papers in Economics 15/19, Division of Economics, School of Business, University of Leicester.
    19. Chaianunporn, Thotsapol & Hovestadt, Thomas, 2012. "Concurrent evolution of random dispersal and habitat niche width in host-parasitoid systems," Ecological Modelling, Elsevier, vol. 247(C), pages 241-250.
    20. Michael B. Doud & Animesh Gupta & Victor Li & Sarah J. Medina & Caesar A. Fuente & Justin R. Meyer, 2024. "Competition-driven eco-evolutionary feedback reshapes bacteriophage lambda’s fitness landscape and enables speciation," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1009417. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.