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The evolution of mechanisms to produce phenotypic heterogeneity in microorganisms

Author

Listed:
  • Guy Alexander Cooper

    (St. John’s College
    University of Oxford)

  • Ming Liu

    (University of Oxford)

  • Jorge Peña

    (University of Toulouse Capitole)

  • Stuart Andrew West

    (University of Oxford)

Abstract

In bacteria and other microorganisms, the cells within a population often show extreme phenotypic variation. Different species use different mechanisms to determine how distinct phenotypes are allocated between individuals, including coordinated, random, and genetic determination. However, it is not clear if this diversity in mechanisms is adaptive—arising because different mechanisms are favoured in different environments—or is merely the result of non-adaptive artifacts of evolution. We use theoretical models to analyse the relative advantages of the two dominant mechanisms to divide labour between reproductives and helpers in microorganisms. We show that coordinated specialisation is more likely to evolve over random specialisation in well-mixed groups when: (i) social groups are small; (ii) helping is more “essential”; and (iii) there is a low metabolic cost to coordination. We find analogous results when we allow for spatial structure with a more detailed model of cellular filaments. More generally, this work shows how diversity in the mechanisms to produce phenotypic heterogeneity could have arisen as adaptations to different environments.

Suggested Citation

  • Guy Alexander Cooper & Ming Liu & Jorge Peña & Stuart Andrew West, 2022. "The evolution of mechanisms to produce phenotypic heterogeneity in microorganisms," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-021-27902-4
    DOI: 10.1038/s41467-021-27902-4
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    Cited by:

    1. Kiyan Shabestary & Cinzia Klemm & Benedict Carling & James Marshall & Juline Savigny & Marko Storch & Rodrigo Ledesma-Amaro, 2024. "Phenotypic heterogeneity follows a growth-viability tradeoff in response to amino acid identity," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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