Abstract: Cooperation is wide-spread and has been postulated to drive major transitions in evolution. A cooperator pays a cost to benefit others, and when reciprocated, it gains a net benefit. However, Darwinian selection favors """"""""cheaters"""""""" that consume benefits without paying a fair cost. Many cooperative systems have evolved sophisticated cheater recognition/exclusion mechanisms. How did cheater-resisting mechanisms evolve from simple cooperative systems? To address this question, I created a genetically tractable cooperative system that can be observed as it evolves, step-by-step, from its inception toward increased stability. It consists of two engineered non-mating yeast strains - a red-fluorescent R strain that requires adenine and releases lysine and a yellow-fluorescent Y strain that requires lysine and releases adenine. I observed that: the system is viable - able to grow from low-density to saturation in the absence of adenine and lysine supplements, over a wide range of conditions; system viability requirements could be calculated from growth, death, and metabolic properties of the two cooperating strains; the system evolved increased system viability: the minimum cell density required for system viability was reduced 100-fold. My group will: discover the diversity of changes that increase system viability. Pro-cooperation changes must act through benefiting self and/or partner. Properties of evolved strains will be measured and their relative contributions to enhanced cooperation will be quantified. determine mechanisms of cheater tolerance. After introducing a cheater that consumes but does not release metabolites, we will select for cooperator/cheater cocultures with increased cheater tolerance and delineate mechanisms. investigate the possibility of spatial structure stabilizing cooperation. We will compare viability requirements and cheater tolerance of the cooperative system in a well-mixed liquid culture (no spatial structure) with those on an agar pad (with spatial structure). We hope to quantitatively understand the evolution of cooperation and cheater tolerance. Public Health Relevance: Cooperation is a fundamental biological phenomenon. For instance, the human body relies on cooperation between different cell types. Diseases can be caused either by cheaters (such as cancer cells) that destroy normal cooperation or by formation of undesired cooperation (such as those found among infecting viruses or bacteria). Discovering and quantifying the importance of mechanisms that drive the evolution of cooperation and cheating may reveal strategies to stabilize or destabilize cooperation.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s New Innovator Awards (DP2)
Project #
1DP2OD006498-01
Application #
7852581
Study Section
Special Emphasis Panel (ZGM1-NDIA-O (02))
Program Officer
Basavappa, Ravi
Project Start
2009-09-30
Project End
2014-06-30
Budget Start
2009-09-30
Budget End
2014-06-30
Support Year
1
Fiscal Year
2009
Total Cost
$2,640,000
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Waite, Adam James; Cannistra, Caroline; Shou, Wenying (2015) Defectors Can Create Conditions That Rescue Cooperation. PLoS Comput Biol 11:e1004645
Waite, Adam James; Shou, Wenying (2014) Constructing synthetic microbial communities to explore the ecology and evolution of symbiosis. Methods Mol Biol 1151:27-38
Green, Robin; Shou, Wenying (2014) Modeling community population dynamics with the open-source language R. Methods Mol Biol 1151:209-31
Momeni, Babak; Waite, Adam James; Shou, Wenying (2013) Spatial self-organization favors heterotypic cooperation over cheating. Elife 2:e00960
Momeni, Babak; Brileya, Kristen A; Fields, Matthew W et al. (2013) Strong inter-population cooperation leads to partner intermixing in microbial communities. Elife 2:e00230
Waite, Adam James; Shou, Wenying (2012) Adaptation to a new environment allows cooperators to purge cheaters stochastically. Proc Natl Acad Sci U S A 109:19079-86
Momeni, Babak; Chen, Chi-Chun; Hillesland, Kristina L et al. (2011) Using artificial systems to explore the ecology and evolution of symbioses. Cell Mol Life Sci 68:1353-68