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Metabolic constraints for a novel symbiosis

Ancient evolutionary events are difficult to study because their current products are derived forms altered by millions of years of adaptation. The primary endosymbiotic event formed the first photosynthetic eukaryote resulting in both plants and algae, with vast consequences for life on Earth. The...

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Autores principales: Sørensen, Megan E. S., Cameron, Duncan D., Brockhurst, Michael A., Wood, A. Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821275/
https://www.ncbi.nlm.nih.gov/pubmed/27069664
http://dx.doi.org/10.1098/rsos.150708
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author Sørensen, Megan E. S.
Cameron, Duncan D.
Brockhurst, Michael A.
Wood, A. Jamie
author_facet Sørensen, Megan E. S.
Cameron, Duncan D.
Brockhurst, Michael A.
Wood, A. Jamie
author_sort Sørensen, Megan E. S.
collection PubMed
description Ancient evolutionary events are difficult to study because their current products are derived forms altered by millions of years of adaptation. The primary endosymbiotic event formed the first photosynthetic eukaryote resulting in both plants and algae, with vast consequences for life on Earth. The evolutionary time that passed since this event means the dominant mechanisms and changes that were required are obscured. Synthetic symbioses such as the novel interaction between Paramecium bursaria and the cyanobacterium Synechocystis PC6803, recently established in the laboratory, permit a unique window on the possible early trajectories of this critical evolutionary event. Here, we apply metabolic modelling, using flux balance analysis (FBA), to predict the metabolic adaptations necessary for this previously free-living symbiont to transition to the endosymbiotic niche. By enforcing reciprocal nutrient trading, we are able to predict the most efficient exchange nutrients for both host and symbiont. During the transition from free-living to obligate symbiosis, it is likely that the trading parameters will change over time, which leads in our model to discontinuous changes in the preferred exchange nutrients. Our results show the applicability of FBA modelling to ancient evolutionary transitions driven by metabolic exchanges, and predict how newly established endosymbioses, governed by conflict, will differ from a well-developed one that has reached a mutual-benefit state.
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spelling pubmed-48212752016-04-11 Metabolic constraints for a novel symbiosis Sørensen, Megan E. S. Cameron, Duncan D. Brockhurst, Michael A. Wood, A. Jamie R Soc Open Sci Biology (Whole Organism) Ancient evolutionary events are difficult to study because their current products are derived forms altered by millions of years of adaptation. The primary endosymbiotic event formed the first photosynthetic eukaryote resulting in both plants and algae, with vast consequences for life on Earth. The evolutionary time that passed since this event means the dominant mechanisms and changes that were required are obscured. Synthetic symbioses such as the novel interaction between Paramecium bursaria and the cyanobacterium Synechocystis PC6803, recently established in the laboratory, permit a unique window on the possible early trajectories of this critical evolutionary event. Here, we apply metabolic modelling, using flux balance analysis (FBA), to predict the metabolic adaptations necessary for this previously free-living symbiont to transition to the endosymbiotic niche. By enforcing reciprocal nutrient trading, we are able to predict the most efficient exchange nutrients for both host and symbiont. During the transition from free-living to obligate symbiosis, it is likely that the trading parameters will change over time, which leads in our model to discontinuous changes in the preferred exchange nutrients. Our results show the applicability of FBA modelling to ancient evolutionary transitions driven by metabolic exchanges, and predict how newly established endosymbioses, governed by conflict, will differ from a well-developed one that has reached a mutual-benefit state. The Royal Society 2016-03-23 /pmc/articles/PMC4821275/ /pubmed/27069664 http://dx.doi.org/10.1098/rsos.150708 Text en http://creativecommons.org/licenses/by/4.0/ © 2016 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Sørensen, Megan E. S.
Cameron, Duncan D.
Brockhurst, Michael A.
Wood, A. Jamie
Metabolic constraints for a novel symbiosis
title Metabolic constraints for a novel symbiosis
title_full Metabolic constraints for a novel symbiosis
title_fullStr Metabolic constraints for a novel symbiosis
title_full_unstemmed Metabolic constraints for a novel symbiosis
title_short Metabolic constraints for a novel symbiosis
title_sort metabolic constraints for a novel symbiosis
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821275/
https://www.ncbi.nlm.nih.gov/pubmed/27069664
http://dx.doi.org/10.1098/rsos.150708
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