Michael Raatz, Arne TraulsenPlease use the format "First name initials family name" as in "Marie S. Curie, Niels H. D. Bohr, Albert Einstein, John R. R. Tolkien, Donna T. Strickland"
<p style="text-align: justify;">When cancers or bacterial infections establish, small populations of cells have to free themselves from homoeostatic regulations that prevent their expansion. Trait evolution allows these populations to evade this regulation, escape stochastic extinction and climb up the fitness landscape. In this study, we analyse this complex process and investigate the fate of a cell population that underlies the basic processes of birth, death and mutation. We find that the shape of the fitness landscape dictates a circular adaptation trajectory in the trait space spanned by birth and death rates. We show that successful adaptation is less likely for parental populations with higher turnover (higher birth and death rates). Including density- or trait-affecting treatment we find that these treatment types change the adaptation dynamics in agreement with a geometrical analysis of fitness gradients. Treatment strategies that simultaneously target birth and death rates are most effective, but also increase evolvability. By mapping physiological adaptation pathways and molecular drug mechanisms to traits and treatments with clear eco-evolutionary consequences, we can achieve a much better understanding of the adaptation dynamics and the eco-evolutionary mechanisms at play in the dynamics of cancer and bacterial infections.</p>
Evolutionary rescue, Resistance evolution, Dormancy, Competitive release, Immune evasion
Michael Doebeli doebeli@zoology.ubc.ca, Jacob Scott scottj10@ccf.org, David Basanta david.basanta@moffitt.org, Anne-Florence Bitbol anne-florence.bitbol@epfl.ch, Rob Noble robert.noble@city.ac.uk, Ville Mustonen v.mustonen@helsinki.fi, Kateřina Staňková k.stankova@maastrichtuniversity.nl
e.g. John Doe john@doe.com
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