Cellular interactions are a major driver for the assembly and functioning of microbial communities. Their strengths are shown to be highly variable in nature; however, it is unclear how such variations regulate community behaviors. Here we construct synthetic Lactococcus lactis consortia and mathematical models to elucidate the role of interaction variability in ecosystem succession and to further determine if casting variability into modeling empowers bottom-up predictions. For a consortium of bacteriocin-mediated cooperation and competition, we find increasing the variations of cooperation, from either altered labor partition or random sampling, drives the community into distinct structures. When the cooperation and competition are additionally modulated by pH, ecosystem succession becomes jointly controlled by the variations of both interactions and yields more diversified dynamics. Mathematical models incorporating variability successfully capture all of these experimental observations. Our study demonstrates interaction variability as a key regulator of community dynamics, providing insights into bottom-up predictions of microbial ecosystems.
One promising frontier for synthetic biology is the development of synthetic ecologies, whereby interacting species form an additional layer of connectivity for engineered gene circuits. Toward this goal, an important step is to understand different types of bacterial interactions in natural settings, among which competition is the most prevalent. By constructing a two-species population dynamics model, here, we mimicked bacterial growth in nature with resource-limited fluctuating environments and searched for optimal strategies for bacterial exploitative competition. In a simple game with two strategy options (constant or susceptible growth), we found that the species playing the constant growth strategy always outplays or is evenly matched with its competitor, suggesting that constant growth is a "no-loss" good bet. We also showed that adoption of sophisticated strategies enables a species to maximize its fitness when its competitor grows susceptibly. The pursuit of fitness maximization is, however, associated with potential loss if both species are capable of strategy adjustment, indicating an intrinsic risk-return trade-off. These findings offer new insights into bacterial competition and may also facilitate the engineering of microbial consortia for synthetic biology applications.
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