Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation

<p>Abstract</p> <p>Background</p> <p>During their lifetime, microbes are exposed to environmental variations, each with its distinct spatio-temporal dynamics. Microbial communities display a remarkable degree of phenotypic plasticity, and highly-fit individuals emerge q...

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Main Authors: Mozhayskiy Vadim, Tagkopoulos Ilias
Format: Article
Language:English
Published: BMC 2012-06-01
Series:BMC Bioinformatics
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spelling doaj-dd6fb5a0c69a420187f0b86fd5f36b492020-11-25T02:34:11ZengBMCBMC Bioinformatics1471-21052012-06-0113Suppl 10S1010.1186/1471-2105-13-S10-S10Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptationMozhayskiy VadimTagkopoulos Ilias<p>Abstract</p> <p>Background</p> <p>During their lifetime, microbes are exposed to environmental variations, each with its distinct spatio-temporal dynamics. Microbial communities display a remarkable degree of phenotypic plasticity, and highly-fit individuals emerge quite rapidly during microbial adaptation to novel environments. However, there exists a high variability when it comes to adaptation potential, and while adaptation occurs rapidly in certain environmental transitions, in others organisms struggle to adapt. Here, we investigate the hypothesis that the rate of evolution can both increase or decrease, depending on the similarity and complexity of the intermediate and final environments. Elucidating such dependencies paves the way towards controlling the rate and direction of evolution, which is of interest to industrial and medical applications.</p> <p>Results</p> <p>Our results show that the rate of evolution can be accelerated by evolving cell populations in sequential combinations of environments that are increasingly more complex. To quantify environmental complexity, we evaluate various information-theoretic metrics, and we provide evidence that multivariate mutual information between environmental signals in a given environment correlates well with the rate of evolution in that environment, as measured in our simulations. We find that strong positive and negative correlations between the intermediate and final environments lead to the increase of evolutionary rates, when the environmental complexity increases. Horizontal Gene Transfer is shown to further augment this acceleration, under certain conditions. Interestingly, our simulations show that weak environmental correlations lead to deceleration of evolution, regardless of environmental complexity. Further analysis of network evolution provides a mechanistic explanation of this phenomenon, as exposing cells to intermediate environments can trap the population to local neighborhoods of sub-optimal fitness.</p>
collection DOAJ
language English
format Article
sources DOAJ
author Mozhayskiy Vadim
Tagkopoulos Ilias
spellingShingle Mozhayskiy Vadim
Tagkopoulos Ilias
Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
BMC Bioinformatics
author_facet Mozhayskiy Vadim
Tagkopoulos Ilias
author_sort Mozhayskiy Vadim
title Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
title_short Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
title_full Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
title_fullStr Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
title_full_unstemmed Guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
title_sort guided evolution of <it>in silico </it>microbial populations in complex environments accelerates evolutionary rates through a step-wise adaptation
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2012-06-01
description <p>Abstract</p> <p>Background</p> <p>During their lifetime, microbes are exposed to environmental variations, each with its distinct spatio-temporal dynamics. Microbial communities display a remarkable degree of phenotypic plasticity, and highly-fit individuals emerge quite rapidly during microbial adaptation to novel environments. However, there exists a high variability when it comes to adaptation potential, and while adaptation occurs rapidly in certain environmental transitions, in others organisms struggle to adapt. Here, we investigate the hypothesis that the rate of evolution can both increase or decrease, depending on the similarity and complexity of the intermediate and final environments. Elucidating such dependencies paves the way towards controlling the rate and direction of evolution, which is of interest to industrial and medical applications.</p> <p>Results</p> <p>Our results show that the rate of evolution can be accelerated by evolving cell populations in sequential combinations of environments that are increasingly more complex. To quantify environmental complexity, we evaluate various information-theoretic metrics, and we provide evidence that multivariate mutual information between environmental signals in a given environment correlates well with the rate of evolution in that environment, as measured in our simulations. We find that strong positive and negative correlations between the intermediate and final environments lead to the increase of evolutionary rates, when the environmental complexity increases. Horizontal Gene Transfer is shown to further augment this acceleration, under certain conditions. Interestingly, our simulations show that weak environmental correlations lead to deceleration of evolution, regardless of environmental complexity. Further analysis of network evolution provides a mechanistic explanation of this phenomenon, as exposing cells to intermediate environments can trap the population to local neighborhoods of sub-optimal fitness.</p>
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