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Long-term experimental evolution decouples size and production costs in Escherichia coli
Body size covaries with population dynamics across life’s domains. Metabolism may impose fundamental constraints on the coevolution of size and demography, but experimental tests of the causal links remain elusive. We leverage a 60,000-generation experiment in which Escherichia coli populations evol...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9173777/ https://www.ncbi.nlm.nih.gov/pubmed/35594402 http://dx.doi.org/10.1073/pnas.2200713119 |
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author | Marshall, Dustin J. Malerba, Martino Lines, Thomas Sezmis, Aysha L. Hasan, Chowdhury M. Lenski, Richard E. McDonald, Michael J. |
author_facet | Marshall, Dustin J. Malerba, Martino Lines, Thomas Sezmis, Aysha L. Hasan, Chowdhury M. Lenski, Richard E. McDonald, Michael J. |
author_sort | Marshall, Dustin J. |
collection | PubMed |
description | Body size covaries with population dynamics across life’s domains. Metabolism may impose fundamental constraints on the coevolution of size and demography, but experimental tests of the causal links remain elusive. We leverage a 60,000-generation experiment in which Escherichia coli populations evolved larger cells to examine intraspecific metabolic scaling and correlations with demographic parameters. Over the course of their evolution, the cells have roughly doubled in size relative to their ancestors. These larger cells have metabolic rates that are absolutely higher, but relative to their size, they are lower. Metabolic theory successfully predicted the relations between size, metabolism, and maximum population density, including support for Damuth’s law of energy equivalence, such that populations of larger cells achieved lower maximum densities but higher maximum biomasses than populations of smaller cells. The scaling of metabolism with cell size thus predicted the scaling of size with maximum population density. In stark contrast to standard theory, however, populations of larger cells grew faster than those of smaller cells, contradicting the fundamental and intuitive assumption that the costs of building new individuals should scale directly with their size. The finding that the costs of production can be decoupled from size necessitates a reevaluation of the evolutionary drivers and ecological consequences of biological size more generally. |
format | Online Article Text |
id | pubmed-9173777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-91737772022-11-20 Long-term experimental evolution decouples size and production costs in Escherichia coli Marshall, Dustin J. Malerba, Martino Lines, Thomas Sezmis, Aysha L. Hasan, Chowdhury M. Lenski, Richard E. McDonald, Michael J. Proc Natl Acad Sci U S A Biological Sciences Body size covaries with population dynamics across life’s domains. Metabolism may impose fundamental constraints on the coevolution of size and demography, but experimental tests of the causal links remain elusive. We leverage a 60,000-generation experiment in which Escherichia coli populations evolved larger cells to examine intraspecific metabolic scaling and correlations with demographic parameters. Over the course of their evolution, the cells have roughly doubled in size relative to their ancestors. These larger cells have metabolic rates that are absolutely higher, but relative to their size, they are lower. Metabolic theory successfully predicted the relations between size, metabolism, and maximum population density, including support for Damuth’s law of energy equivalence, such that populations of larger cells achieved lower maximum densities but higher maximum biomasses than populations of smaller cells. The scaling of metabolism with cell size thus predicted the scaling of size with maximum population density. In stark contrast to standard theory, however, populations of larger cells grew faster than those of smaller cells, contradicting the fundamental and intuitive assumption that the costs of building new individuals should scale directly with their size. The finding that the costs of production can be decoupled from size necessitates a reevaluation of the evolutionary drivers and ecological consequences of biological size more generally. National Academy of Sciences 2022-05-20 2022-05-24 /pmc/articles/PMC9173777/ /pubmed/35594402 http://dx.doi.org/10.1073/pnas.2200713119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Marshall, Dustin J. Malerba, Martino Lines, Thomas Sezmis, Aysha L. Hasan, Chowdhury M. Lenski, Richard E. McDonald, Michael J. Long-term experimental evolution decouples size and production costs in Escherichia coli |
title | Long-term experimental evolution decouples size and production costs in Escherichia coli |
title_full | Long-term experimental evolution decouples size and production costs in Escherichia coli |
title_fullStr | Long-term experimental evolution decouples size and production costs in Escherichia coli |
title_full_unstemmed | Long-term experimental evolution decouples size and production costs in Escherichia coli |
title_short | Long-term experimental evolution decouples size and production costs in Escherichia coli |
title_sort | long-term experimental evolution decouples size and production costs in escherichia coli |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9173777/ https://www.ncbi.nlm.nih.gov/pubmed/35594402 http://dx.doi.org/10.1073/pnas.2200713119 |
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