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Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models

Understanding the adaptive responses of individual bacterial strains is crucial for microbiome engineering approaches that introduce new functionalities into complex microbiomes, such as xenobiotic compound metabolism for soil bioremediation. Adaptation requires metabolic reprogramming of the cell,...

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Autores principales: Hadadi, Noushin, Pandey, Vikash, Chiappino-Pepe, Anush, Morales, Marian, Gallart-Ayala, Hector, Mehl, Florence, Ivanisevic, Julijana, Sentchilo, Vladimir, Meer, Jan R. van der
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946695/
https://www.ncbi.nlm.nih.gov/pubmed/32001719
http://dx.doi.org/10.1038/s41540-019-0121-4
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author Hadadi, Noushin
Pandey, Vikash
Chiappino-Pepe, Anush
Morales, Marian
Gallart-Ayala, Hector
Mehl, Florence
Ivanisevic, Julijana
Sentchilo, Vladimir
Meer, Jan R. van der
author_facet Hadadi, Noushin
Pandey, Vikash
Chiappino-Pepe, Anush
Morales, Marian
Gallart-Ayala, Hector
Mehl, Florence
Ivanisevic, Julijana
Sentchilo, Vladimir
Meer, Jan R. van der
author_sort Hadadi, Noushin
collection PubMed
description Understanding the adaptive responses of individual bacterial strains is crucial for microbiome engineering approaches that introduce new functionalities into complex microbiomes, such as xenobiotic compound metabolism for soil bioremediation. Adaptation requires metabolic reprogramming of the cell, which can be captured by multi-omics, but this data remains formidably challenging to interpret and predict. Here we present a new approach that combines genome-scale metabolic modeling with transcriptomics and exometabolomics, both of which are common tools for studying dynamic population behavior. As a realistic demonstration, we developed a genome-scale model of Pseudomonas veronii 1YdBTEX2, a candidate bioaugmentation agent for accelerated metabolism of mono-aromatic compounds in soil microbiomes, while simultaneously collecting experimental data of P. veronii metabolism during growth phase transitions. Predictions of the P. veronii growth rates and specific metabolic processes from the integrated model closely matched experimental observations. We conclude that integrative and network-based analysis can help build predictive models that accurately capture bacterial adaptation responses. Further development and testing of such models may considerably improve the successful establishment of bacterial inoculants in more complex systems.
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spelling pubmed-69466952020-01-13 Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models Hadadi, Noushin Pandey, Vikash Chiappino-Pepe, Anush Morales, Marian Gallart-Ayala, Hector Mehl, Florence Ivanisevic, Julijana Sentchilo, Vladimir Meer, Jan R. van der NPJ Syst Biol Appl Article Understanding the adaptive responses of individual bacterial strains is crucial for microbiome engineering approaches that introduce new functionalities into complex microbiomes, such as xenobiotic compound metabolism for soil bioremediation. Adaptation requires metabolic reprogramming of the cell, which can be captured by multi-omics, but this data remains formidably challenging to interpret and predict. Here we present a new approach that combines genome-scale metabolic modeling with transcriptomics and exometabolomics, both of which are common tools for studying dynamic population behavior. As a realistic demonstration, we developed a genome-scale model of Pseudomonas veronii 1YdBTEX2, a candidate bioaugmentation agent for accelerated metabolism of mono-aromatic compounds in soil microbiomes, while simultaneously collecting experimental data of P. veronii metabolism during growth phase transitions. Predictions of the P. veronii growth rates and specific metabolic processes from the integrated model closely matched experimental observations. We conclude that integrative and network-based analysis can help build predictive models that accurately capture bacterial adaptation responses. Further development and testing of such models may considerably improve the successful establishment of bacterial inoculants in more complex systems. Nature Publishing Group UK 2020-01-07 /pmc/articles/PMC6946695/ /pubmed/32001719 http://dx.doi.org/10.1038/s41540-019-0121-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hadadi, Noushin
Pandey, Vikash
Chiappino-Pepe, Anush
Morales, Marian
Gallart-Ayala, Hector
Mehl, Florence
Ivanisevic, Julijana
Sentchilo, Vladimir
Meer, Jan R. van der
Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
title Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
title_full Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
title_fullStr Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
title_full_unstemmed Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
title_short Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
title_sort mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946695/
https://www.ncbi.nlm.nih.gov/pubmed/32001719
http://dx.doi.org/10.1038/s41540-019-0121-4
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