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Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy
Pseudomonas aeruginosa is a globally-distributed bacterium often found in medical infections. The opportunistic pathogen uses a different, carbon catabolite repression (CCR) strategy than many, model microorganisms. It does not utilize a classic diauxie phenotype, nor does it follow common systems b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809481/ https://www.ncbi.nlm.nih.gov/pubmed/33446818 http://dx.doi.org/10.1038/s41598-020-80522-8 |
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author | McGill, S. Lee Yung, Yeni Hunt, Kristopher A. Henson, Michael A. Hanley, Luke Carlson, Ross P. |
author_facet | McGill, S. Lee Yung, Yeni Hunt, Kristopher A. Henson, Michael A. Hanley, Luke Carlson, Ross P. |
author_sort | McGill, S. Lee |
collection | PubMed |
description | Pseudomonas aeruginosa is a globally-distributed bacterium often found in medical infections. The opportunistic pathogen uses a different, carbon catabolite repression (CCR) strategy than many, model microorganisms. It does not utilize a classic diauxie phenotype, nor does it follow common systems biology assumptions including preferential consumption of glucose with an ‘overflow’ metabolism. Despite these contradictions, P. aeruginosa is competitive in many, disparate environments underscoring knowledge gaps in microbial ecology and systems biology. Physiological, omics, and in silico analyses were used to quantify the P. aeruginosa CCR strategy known as ‘reverse diauxie’. An ecological basis of reverse diauxie was identified using a genome-scale, metabolic model interrogated with in vitro omics data. Reverse diauxie preference for lower energy, nonfermentable carbon sources, such as acetate or succinate over glucose, was predicted using a multidimensional strategy which minimized resource investment into central metabolism while completely oxidizing substrates. Application of a common, in silico optimization criterion, which maximizes growth rate, did not predict the reverse diauxie phenotypes. This study quantifies P. aeruginosa metabolic strategies foundational to its wide distribution and virulence including its potentially, mutualistic interactions with microorganisms found commonly in the environment and in medical infections. |
format | Online Article Text |
id | pubmed-7809481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78094812021-01-21 Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy McGill, S. Lee Yung, Yeni Hunt, Kristopher A. Henson, Michael A. Hanley, Luke Carlson, Ross P. Sci Rep Article Pseudomonas aeruginosa is a globally-distributed bacterium often found in medical infections. The opportunistic pathogen uses a different, carbon catabolite repression (CCR) strategy than many, model microorganisms. It does not utilize a classic diauxie phenotype, nor does it follow common systems biology assumptions including preferential consumption of glucose with an ‘overflow’ metabolism. Despite these contradictions, P. aeruginosa is competitive in many, disparate environments underscoring knowledge gaps in microbial ecology and systems biology. Physiological, omics, and in silico analyses were used to quantify the P. aeruginosa CCR strategy known as ‘reverse diauxie’. An ecological basis of reverse diauxie was identified using a genome-scale, metabolic model interrogated with in vitro omics data. Reverse diauxie preference for lower energy, nonfermentable carbon sources, such as acetate or succinate over glucose, was predicted using a multidimensional strategy which minimized resource investment into central metabolism while completely oxidizing substrates. Application of a common, in silico optimization criterion, which maximizes growth rate, did not predict the reverse diauxie phenotypes. This study quantifies P. aeruginosa metabolic strategies foundational to its wide distribution and virulence including its potentially, mutualistic interactions with microorganisms found commonly in the environment and in medical infections. Nature Publishing Group UK 2021-01-14 /pmc/articles/PMC7809481/ /pubmed/33446818 http://dx.doi.org/10.1038/s41598-020-80522-8 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article McGill, S. Lee Yung, Yeni Hunt, Kristopher A. Henson, Michael A. Hanley, Luke Carlson, Ross P. Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
title | Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
title_full | Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
title_fullStr | Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
title_full_unstemmed | Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
title_short | Pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
title_sort | pseudomonas aeruginosa reverse diauxie is a multidimensional, optimized, resource utilization strategy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809481/ https://www.ncbi.nlm.nih.gov/pubmed/33446818 http://dx.doi.org/10.1038/s41598-020-80522-8 |
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