1–26 Jul 2019
Nordita, Stockholm
Europe/Stockholm timezone

Forecasting experimental evolution in Pseudomonas

3 Jul 2019, 09:30
1h
FB52 (Nordita, Stockholm)

FB52

Nordita, Stockholm

Speaker

Peter Lind

Description

Previous work on the adaptive “wrinkly spreader” (WS) type in Pseudomonas fluorescens allowed us to develop models and rules to predict evolutionary outcomes. Knowledge of the genotype-to- phenotype map of the WS phenotype and of alternative phenotypic solutions to the problem of air-liquid interface colonization allows forecasting for related species. Equipped with the genome sequences of P. protegens and P. syringae combined with knowledge from work in P. fluorescens, predictions about the outcome of experimental evolution were made. Phenotypic predictions were successful in terms of the exopolymeric substances (EPSs) structural components used to colonize the air-liquid interface caused by mutational activation of diaguanylate cyclases (DGCs). As predicted, the most common mutation type was loss-of-function mutation followed by less common promoter mutations and promoter capture events. Although up to 39 different DGCs are encoded in these genomes the relative rates of the top two or four was successfully predicted. Individual mutations could not be predicted, but the mutated regions were conserved between species with the majority of mutations expected to disrupt intermolecular or interdomain interactions. Mutational hot spots were not conserved between species. This work shows the potential of extending one of the best- characterized experimental evolution systems to other species allowing true testing of evolutionary forecasts. Frequent horizontal gene transfer and gene loss of DGCs and genes encoding structural EPSs creates a large diversity among different Pseudomonas species meaning that the prediction is different for each species. This allows an iterative workflow of prediction, experimental evolution and model improvement to explore the limits of evolutionary forecasting. There is potential for collaborations on many levels including development and testing of methods for predictions on different biological levels, theoretical considerations and modelling as well as comparisons with other experimental systems.

Primary author

Peter Lind

Presentation materials

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