Cargando…

Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations

Efficient production of ethanol for use as a renewable fuel requires organisms with a high level of ethanol tolerance. However, this trait is complex and increased tolerance therefore requires mutations in multiple genes and pathways. Here, we use experimental evolution for a system-level analysis o...

Descripción completa

Detalles Bibliográficos
Autores principales: Swings, Toon, Weytjens, Bram, Schalck, Thomas, Bonte, Camille, Verstraeten, Natalie, Michiels, Jan, Marchal, Kathleen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850225/
https://www.ncbi.nlm.nih.gov/pubmed/28961727
http://dx.doi.org/10.1093/molbev/msx228
_version_ 1783306194626019328
author Swings, Toon
Weytjens, Bram
Schalck, Thomas
Bonte, Camille
Verstraeten, Natalie
Michiels, Jan
Marchal, Kathleen
author_facet Swings, Toon
Weytjens, Bram
Schalck, Thomas
Bonte, Camille
Verstraeten, Natalie
Michiels, Jan
Marchal, Kathleen
author_sort Swings, Toon
collection PubMed
description Efficient production of ethanol for use as a renewable fuel requires organisms with a high level of ethanol tolerance. However, this trait is complex and increased tolerance therefore requires mutations in multiple genes and pathways. Here, we use experimental evolution for a system-level analysis of adaptation of Escherichia coli to high ethanol stress. As adaptation to extreme stress often results in complex mutational data sets consisting of both causal and noncausal passenger mutations, identifying the true adaptive mutations in these settings is not trivial. Therefore, we developed a novel method named IAMBEE (Identification of Adaptive Mutations in Bacterial Evolution Experiments). IAMBEE exploits the temporal profile of the acquisition of mutations during evolution in combination with the functional implications of each mutation at the protein level. These data are mapped to a genome-wide interaction network to search for adaptive mutations at the level of pathways. The 16 evolved populations in our data set together harbored 2,286 mutated genes with 4,470 unique mutations. Analysis by IAMBEE significantly reduced this number and resulted in identification of 90 mutated genes and 345 unique mutations that are most likely to be adaptive. Moreover, IAMBEE not only enabled the identification of previously known pathways involved in ethanol tolerance, but also identified novel systems such as the AcrAB-TolC efflux pump and fatty acids biosynthesis and even allowed to gain insight into the temporal profile of adaptation to ethanol stress. Furthermore, this method offers a solid framework for identifying the molecular underpinnings of other complex traits as well.
format Online
Article
Text
id pubmed-5850225
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-58502252018-03-23 Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations Swings, Toon Weytjens, Bram Schalck, Thomas Bonte, Camille Verstraeten, Natalie Michiels, Jan Marchal, Kathleen Mol Biol Evol Discoveries Efficient production of ethanol for use as a renewable fuel requires organisms with a high level of ethanol tolerance. However, this trait is complex and increased tolerance therefore requires mutations in multiple genes and pathways. Here, we use experimental evolution for a system-level analysis of adaptation of Escherichia coli to high ethanol stress. As adaptation to extreme stress often results in complex mutational data sets consisting of both causal and noncausal passenger mutations, identifying the true adaptive mutations in these settings is not trivial. Therefore, we developed a novel method named IAMBEE (Identification of Adaptive Mutations in Bacterial Evolution Experiments). IAMBEE exploits the temporal profile of the acquisition of mutations during evolution in combination with the functional implications of each mutation at the protein level. These data are mapped to a genome-wide interaction network to search for adaptive mutations at the level of pathways. The 16 evolved populations in our data set together harbored 2,286 mutated genes with 4,470 unique mutations. Analysis by IAMBEE significantly reduced this number and resulted in identification of 90 mutated genes and 345 unique mutations that are most likely to be adaptive. Moreover, IAMBEE not only enabled the identification of previously known pathways involved in ethanol tolerance, but also identified novel systems such as the AcrAB-TolC efflux pump and fatty acids biosynthesis and even allowed to gain insight into the temporal profile of adaptation to ethanol stress. Furthermore, this method offers a solid framework for identifying the molecular underpinnings of other complex traits as well. Oxford University Press 2017-11 2017-08-28 /pmc/articles/PMC5850225/ /pubmed/28961727 http://dx.doi.org/10.1093/molbev/msx228 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Swings, Toon
Weytjens, Bram
Schalck, Thomas
Bonte, Camille
Verstraeten, Natalie
Michiels, Jan
Marchal, Kathleen
Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations
title Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations
title_full Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations
title_fullStr Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations
title_full_unstemmed Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations
title_short Network-Based Identification of Adaptive Pathways in Evolved Ethanol-Tolerant Bacterial Populations
title_sort network-based identification of adaptive pathways in evolved ethanol-tolerant bacterial populations
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850225/
https://www.ncbi.nlm.nih.gov/pubmed/28961727
http://dx.doi.org/10.1093/molbev/msx228
work_keys_str_mv AT swingstoon networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations
AT weytjensbram networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations
AT schalckthomas networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations
AT bontecamille networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations
AT verstraetennatalie networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations
AT michielsjan networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations
AT marchalkathleen networkbasedidentificationofadaptivepathwaysinevolvedethanoltolerantbacterialpopulations