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Noisy metabolism can promote microbial cross-feeding
Cross-feeding, the exchange of nutrients between organisms, is ubiquitous in microbial communities. Despite its importance in natural and engineered microbial systems, our understanding of how inter-species cross-feeding arises is incomplete, with existing theories limited to specific scenarios. Her...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983042/ https://www.ncbi.nlm.nih.gov/pubmed/35380535 http://dx.doi.org/10.7554/eLife.70694 |
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author | Lopez, Jaime G Wingreen, Ned S |
author_facet | Lopez, Jaime G Wingreen, Ned S |
author_sort | Lopez, Jaime G |
collection | PubMed |
description | Cross-feeding, the exchange of nutrients between organisms, is ubiquitous in microbial communities. Despite its importance in natural and engineered microbial systems, our understanding of how inter-species cross-feeding arises is incomplete, with existing theories limited to specific scenarios. Here, we introduce a novel theory for the emergence of such cross-feeding, which we term noise-averaging cooperation (NAC). NAC is based on the idea that, due to their small size, bacteria are prone to noisy regulation of metabolism which limits their growth rate. To compensate, related bacteria can share metabolites with each other to ‘average out’ noise and improve their collective growth. According to the Black Queen Hypothesis, this metabolite sharing among kin, a form of ‘leakage’, then allows for the evolution of metabolic interdependencies among species including de novo speciation via gene deletions. We first characterize NAC in a simple ecological model of cell metabolism, showing that metabolite leakage can in principle substantially increase growth rate in a community context. Next, we develop a generalized framework for estimating the potential benefits of NAC among real bacteria. Using single-cell protein abundance data, we predict that bacteria suffer from substantial noise-driven growth inefficiencies, and may therefore benefit from NAC. We then discuss potential evolutionary pathways for the emergence of NAC. Finally, we review existing evidence for NAC and outline potential experimental approaches to detect NAC in microbial communities. |
format | Online Article Text |
id | pubmed-8983042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89830422022-04-06 Noisy metabolism can promote microbial cross-feeding Lopez, Jaime G Wingreen, Ned S eLife Ecology Cross-feeding, the exchange of nutrients between organisms, is ubiquitous in microbial communities. Despite its importance in natural and engineered microbial systems, our understanding of how inter-species cross-feeding arises is incomplete, with existing theories limited to specific scenarios. Here, we introduce a novel theory for the emergence of such cross-feeding, which we term noise-averaging cooperation (NAC). NAC is based on the idea that, due to their small size, bacteria are prone to noisy regulation of metabolism which limits their growth rate. To compensate, related bacteria can share metabolites with each other to ‘average out’ noise and improve their collective growth. According to the Black Queen Hypothesis, this metabolite sharing among kin, a form of ‘leakage’, then allows for the evolution of metabolic interdependencies among species including de novo speciation via gene deletions. We first characterize NAC in a simple ecological model of cell metabolism, showing that metabolite leakage can in principle substantially increase growth rate in a community context. Next, we develop a generalized framework for estimating the potential benefits of NAC among real bacteria. Using single-cell protein abundance data, we predict that bacteria suffer from substantial noise-driven growth inefficiencies, and may therefore benefit from NAC. We then discuss potential evolutionary pathways for the emergence of NAC. Finally, we review existing evidence for NAC and outline potential experimental approaches to detect NAC in microbial communities. eLife Sciences Publications, Ltd 2022-04-05 /pmc/articles/PMC8983042/ /pubmed/35380535 http://dx.doi.org/10.7554/eLife.70694 Text en © 2022, Lopez and Wingreen https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Ecology Lopez, Jaime G Wingreen, Ned S Noisy metabolism can promote microbial cross-feeding |
title | Noisy metabolism can promote microbial cross-feeding |
title_full | Noisy metabolism can promote microbial cross-feeding |
title_fullStr | Noisy metabolism can promote microbial cross-feeding |
title_full_unstemmed | Noisy metabolism can promote microbial cross-feeding |
title_short | Noisy metabolism can promote microbial cross-feeding |
title_sort | noisy metabolism can promote microbial cross-feeding |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983042/ https://www.ncbi.nlm.nih.gov/pubmed/35380535 http://dx.doi.org/10.7554/eLife.70694 |
work_keys_str_mv | AT lopezjaimeg noisymetabolismcanpromotemicrobialcrossfeeding AT wingreenneds noisymetabolismcanpromotemicrobialcrossfeeding |