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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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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. |
format | Online Article Text |
id | pubmed-10427823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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