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Epistasis decreases with increasing antibiotic pressure but not temperature

Predicting mutational effects is essential for the control of antibiotic resistance (ABR). Predictions are difficult when there are strong genotype-by-environment (G × E), gene-by-gene (G × G or epistatic) or gene-by-gene-by-environment (G × G × E) interactions. We quantified G × G × E effects in Es...

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Detalles Bibliográficos
Autores principales: Ghenu, Ana-Hermina, Amado, André, Gordo, Isabel, Bank, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067269/
https://www.ncbi.nlm.nih.gov/pubmed/37004727
http://dx.doi.org/10.1098/rstb.2022.0058
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author Ghenu, Ana-Hermina
Amado, André
Gordo, Isabel
Bank, Claudia
author_facet Ghenu, Ana-Hermina
Amado, André
Gordo, Isabel
Bank, Claudia
author_sort Ghenu, Ana-Hermina
collection PubMed
description Predicting mutational effects is essential for the control of antibiotic resistance (ABR). Predictions are difficult when there are strong genotype-by-environment (G × E), gene-by-gene (G × G or epistatic) or gene-by-gene-by-environment (G × G × E) interactions. We quantified G × G × E effects in Escherichia coli across environmental gradients. We created intergenic fitness landscapes using gene knock-outs and single-nucleotide ABR mutations previously identified to vary in the extent of G × E effects in our environments of interest. Then, we measured competitive fitness across a complete combinatorial set of temperature and antibiotic dosage gradients. In this way, we assessed the predictability of 15 fitness landscapes across 12 different but related environments. We found G × G interactions and rugged fitness landscapes in the absence of antibiotic, but as antibiotic concentration increased, the fitness effects of ABR genotypes quickly overshadowed those of gene knock-outs, and the landscapes became smoother. Our work reiterates that some single mutants, like those conferring resistance or susceptibility to antibiotics, have consistent effects across genetic backgrounds in stressful environments. Thus, although epistasis may reduce the predictability of evolution in benign environments, evolution may be more predictable in adverse environments. This article is part of the theme issue ‘Interdisciplinary approaches to predicting evolutionary biology’.
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spelling pubmed-100672692023-04-03 Epistasis decreases with increasing antibiotic pressure but not temperature Ghenu, Ana-Hermina Amado, André Gordo, Isabel Bank, Claudia Philos Trans R Soc Lond B Biol Sci Articles Predicting mutational effects is essential for the control of antibiotic resistance (ABR). Predictions are difficult when there are strong genotype-by-environment (G × E), gene-by-gene (G × G or epistatic) or gene-by-gene-by-environment (G × G × E) interactions. We quantified G × G × E effects in Escherichia coli across environmental gradients. We created intergenic fitness landscapes using gene knock-outs and single-nucleotide ABR mutations previously identified to vary in the extent of G × E effects in our environments of interest. Then, we measured competitive fitness across a complete combinatorial set of temperature and antibiotic dosage gradients. In this way, we assessed the predictability of 15 fitness landscapes across 12 different but related environments. We found G × G interactions and rugged fitness landscapes in the absence of antibiotic, but as antibiotic concentration increased, the fitness effects of ABR genotypes quickly overshadowed those of gene knock-outs, and the landscapes became smoother. Our work reiterates that some single mutants, like those conferring resistance or susceptibility to antibiotics, have consistent effects across genetic backgrounds in stressful environments. Thus, although epistasis may reduce the predictability of evolution in benign environments, evolution may be more predictable in adverse environments. This article is part of the theme issue ‘Interdisciplinary approaches to predicting evolutionary biology’. The Royal Society 2023-05-22 2023-04-03 /pmc/articles/PMC10067269/ /pubmed/37004727 http://dx.doi.org/10.1098/rstb.2022.0058 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Ghenu, Ana-Hermina
Amado, André
Gordo, Isabel
Bank, Claudia
Epistasis decreases with increasing antibiotic pressure but not temperature
title Epistasis decreases with increasing antibiotic pressure but not temperature
title_full Epistasis decreases with increasing antibiotic pressure but not temperature
title_fullStr Epistasis decreases with increasing antibiotic pressure but not temperature
title_full_unstemmed Epistasis decreases with increasing antibiotic pressure but not temperature
title_short Epistasis decreases with increasing antibiotic pressure but not temperature
title_sort epistasis decreases with increasing antibiotic pressure but not temperature
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067269/
https://www.ncbi.nlm.nih.gov/pubmed/37004727
http://dx.doi.org/10.1098/rstb.2022.0058
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