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The population genetics of collateral resistance and sensitivity

Resistance mutations against one drug can elicit collateral sensitivity against other drugs. Multi-drug treatments exploiting such trade-offs can help slow down the evolution of resistance. However, if mutations with diverse collateral effects are available, a treated population may evolve either co...

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Detalles Bibliográficos
Autores principales: Ardell, Sarah M, Kryazhimskiy, Sergey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765753/
https://www.ncbi.nlm.nih.gov/pubmed/34889185
http://dx.doi.org/10.7554/eLife.73250
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author Ardell, Sarah M
Kryazhimskiy, Sergey
author_facet Ardell, Sarah M
Kryazhimskiy, Sergey
author_sort Ardell, Sarah M
collection PubMed
description Resistance mutations against one drug can elicit collateral sensitivity against other drugs. Multi-drug treatments exploiting such trade-offs can help slow down the evolution of resistance. However, if mutations with diverse collateral effects are available, a treated population may evolve either collateral sensitivity or collateral resistance. How to design treatments robust to such uncertainty is unclear. We show that many resistance mutations in Escherichia coli against various antibiotics indeed have diverse collateral effects. We propose to characterize such diversity with a joint distribution of fitness effects (JDFE) and develop a theory for describing and predicting collateral evolution based on simple statistics of the JDFE. We show how to robustly rank drug pairs to minimize the risk of collateral resistance and how to estimate JDFEs. In addition to practical applications, these results have implications for our understanding of evolution in variable environments.
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spelling pubmed-87657532022-01-19 The population genetics of collateral resistance and sensitivity Ardell, Sarah M Kryazhimskiy, Sergey eLife Evolutionary Biology Resistance mutations against one drug can elicit collateral sensitivity against other drugs. Multi-drug treatments exploiting such trade-offs can help slow down the evolution of resistance. However, if mutations with diverse collateral effects are available, a treated population may evolve either collateral sensitivity or collateral resistance. How to design treatments robust to such uncertainty is unclear. We show that many resistance mutations in Escherichia coli against various antibiotics indeed have diverse collateral effects. We propose to characterize such diversity with a joint distribution of fitness effects (JDFE) and develop a theory for describing and predicting collateral evolution based on simple statistics of the JDFE. We show how to robustly rank drug pairs to minimize the risk of collateral resistance and how to estimate JDFEs. In addition to practical applications, these results have implications for our understanding of evolution in variable environments. eLife Sciences Publications, Ltd 2021-12-10 /pmc/articles/PMC8765753/ /pubmed/34889185 http://dx.doi.org/10.7554/eLife.73250 Text en © 2021, Ardell and Kryazhimskiy 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 Evolutionary Biology
Ardell, Sarah M
Kryazhimskiy, Sergey
The population genetics of collateral resistance and sensitivity
title The population genetics of collateral resistance and sensitivity
title_full The population genetics of collateral resistance and sensitivity
title_fullStr The population genetics of collateral resistance and sensitivity
title_full_unstemmed The population genetics of collateral resistance and sensitivity
title_short The population genetics of collateral resistance and sensitivity
title_sort population genetics of collateral resistance and sensitivity
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765753/
https://www.ncbi.nlm.nih.gov/pubmed/34889185
http://dx.doi.org/10.7554/eLife.73250
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