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Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations

The fitness effects of antibiotic resistance mutations are a major driver of resistance evolution. While the nutrient environment affects bacterial fitness, experimental studies of resistance typically measure fitness of mutants in a single environment only. We explored how the nutrient environment...

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Autores principales: Soley, Jake K., Jago, Matthew, Walsh, Calum J., Khomarbaghi, Zahra, Howden, Benjamin P., Lagator, Mato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427823/
https://www.ncbi.nlm.nih.gov/pubmed/37583318
http://dx.doi.org/10.1098/rspb.2023.1030
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author Soley, Jake K.
Jago, Matthew
Walsh, Calum J.
Khomarbaghi, Zahra
Howden, Benjamin P.
Lagator, Mato
author_facet Soley, Jake K.
Jago, Matthew
Walsh, Calum J.
Khomarbaghi, Zahra
Howden, Benjamin P.
Lagator, Mato
author_sort Soley, Jake K.
collection PubMed
description The fitness effects of antibiotic resistance mutations are a major driver of resistance evolution. While the nutrient environment affects bacterial fitness, experimental studies of resistance typically measure fitness of mutants in a single environment only. We explored how the nutrient environment affected the fitness effects of rifampicin-resistant rpoB mutations in Escherichia coli under several conditions critical for the emergence and spread of resistance—the presence of primary or secondary antibiotic, or the absence of any antibiotic. Pervasive genotype-by-environment (GxE) interactions determined fitness in all experimental conditions, with rank order of fitness in the presence and absence of antibiotics being strongly dependent on the nutrient environment. GxE interactions also affected the magnitude and direction of collateral effects of secondary antibiotics, in some cases so drastically that a mutant that was highly sensitive in one nutrient environment exhibited cross-resistance to the same antibiotic in another. It is likely that the mutant-specific impact of rpoB mutations on the global transcriptome underpins the observed GxE interactions. The pervasive, mutant-specific GxE interactions highlight the importance of doing what is rarely done when studying the evolution and spread of resistance in experimental and clinical work: assessing fitness of antibiotic-resistant mutants across a range of relevant environments.
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spelling pubmed-104278232023-08-17 Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations Soley, Jake K. Jago, Matthew Walsh, Calum J. Khomarbaghi, Zahra Howden, Benjamin P. Lagator, Mato Proc Biol Sci Evolution The fitness effects of antibiotic resistance mutations are a major driver of resistance evolution. While the nutrient environment affects bacterial fitness, experimental studies of resistance typically measure fitness of mutants in a single environment only. We explored how the nutrient environment affected the fitness effects of rifampicin-resistant rpoB mutations in Escherichia coli under several conditions critical for the emergence and spread of resistance—the presence of primary or secondary antibiotic, or the absence of any antibiotic. Pervasive genotype-by-environment (GxE) interactions determined fitness in all experimental conditions, with rank order of fitness in the presence and absence of antibiotics being strongly dependent on the nutrient environment. GxE interactions also affected the magnitude and direction of collateral effects of secondary antibiotics, in some cases so drastically that a mutant that was highly sensitive in one nutrient environment exhibited cross-resistance to the same antibiotic in another. It is likely that the mutant-specific impact of rpoB mutations on the global transcriptome underpins the observed GxE interactions. The pervasive, mutant-specific GxE interactions highlight the importance of doing what is rarely done when studying the evolution and spread of resistance in experimental and clinical work: assessing fitness of antibiotic-resistant mutants across a range of relevant environments. The Royal Society 2023-08-30 2023-08-16 /pmc/articles/PMC10427823/ /pubmed/37583318 http://dx.doi.org/10.1098/rspb.2023.1030 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 Evolution
Soley, Jake K.
Jago, Matthew
Walsh, Calum J.
Khomarbaghi, Zahra
Howden, Benjamin P.
Lagator, Mato
Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
title Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
title_full Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
title_fullStr Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
title_full_unstemmed Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
title_short Pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
title_sort pervasive genotype-by-environment interactions shape the fitness effects of antibiotic resistance mutations
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427823/
https://www.ncbi.nlm.nih.gov/pubmed/37583318
http://dx.doi.org/10.1098/rspb.2023.1030
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