Cargando…
Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations
Multidrug-resistant clinical isolates are common in certain pathogens, but rare in others. This pattern may be due to the fact that mutations shaping resistance have species-specific effects. To investigate this issue, we transferred a range of resistance-conferring mutations and a full resistance g...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657729/ https://www.ncbi.nlm.nih.gov/pubmed/31058961 http://dx.doi.org/10.1093/molbev/msz109 |
_version_ | 1783438841747603456 |
---|---|
author | Apjok, Gábor Boross, Gábor Nyerges, Ákos Fekete, Gergely Lázár, Viktória Papp, Balázs Pál, Csaba Csörgő, Bálint |
author_facet | Apjok, Gábor Boross, Gábor Nyerges, Ákos Fekete, Gergely Lázár, Viktória Papp, Balázs Pál, Csaba Csörgő, Bálint |
author_sort | Apjok, Gábor |
collection | PubMed |
description | Multidrug-resistant clinical isolates are common in certain pathogens, but rare in others. This pattern may be due to the fact that mutations shaping resistance have species-specific effects. To investigate this issue, we transferred a range of resistance-conferring mutations and a full resistance gene into Escherichia coli and closely related bacteria. We found that resistance mutations in one bacterial species frequently provide no resistance, in fact even yielding drug hypersensitivity in close relatives. In depth analysis of a key gene involved in aminoglycoside resistance (trkH) indicated that preexisting mutations in other genes—intergenic epistasis—underlie such extreme differences in mutational effects between species. Finally, reconstruction of adaptive landscapes under multiple antibiotic stresses revealed that mutations frequently provide multidrug resistance or elevated drug susceptibility (i.e., collateral sensitivity) only with certain combinations of other resistance mutations. We conclude that resistance and collateral sensitivity are contingent upon the genetic makeup of the bacterial population, and such contingency could shape the long-term fate of resistant bacteria. These results underlie the importance of species-specific treatment strategies. |
format | Online Article Text |
id | pubmed-6657729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66577292019-08-02 Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations Apjok, Gábor Boross, Gábor Nyerges, Ákos Fekete, Gergely Lázár, Viktória Papp, Balázs Pál, Csaba Csörgő, Bálint Mol Biol Evol Fast Track Multidrug-resistant clinical isolates are common in certain pathogens, but rare in others. This pattern may be due to the fact that mutations shaping resistance have species-specific effects. To investigate this issue, we transferred a range of resistance-conferring mutations and a full resistance gene into Escherichia coli and closely related bacteria. We found that resistance mutations in one bacterial species frequently provide no resistance, in fact even yielding drug hypersensitivity in close relatives. In depth analysis of a key gene involved in aminoglycoside resistance (trkH) indicated that preexisting mutations in other genes—intergenic epistasis—underlie such extreme differences in mutational effects between species. Finally, reconstruction of adaptive landscapes under multiple antibiotic stresses revealed that mutations frequently provide multidrug resistance or elevated drug susceptibility (i.e., collateral sensitivity) only with certain combinations of other resistance mutations. We conclude that resistance and collateral sensitivity are contingent upon the genetic makeup of the bacterial population, and such contingency could shape the long-term fate of resistant bacteria. These results underlie the importance of species-specific treatment strategies. Oxford University Press 2019-08 2019-05-06 /pmc/articles/PMC6657729/ /pubmed/31058961 http://dx.doi.org/10.1093/molbev/msz109 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Fast Track Apjok, Gábor Boross, Gábor Nyerges, Ákos Fekete, Gergely Lázár, Viktória Papp, Balázs Pál, Csaba Csörgő, Bálint Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations |
title | Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations |
title_full | Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations |
title_fullStr | Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations |
title_full_unstemmed | Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations |
title_short | Limited Evolutionary Conservation of the Phenotypic Effects of Antibiotic Resistance Mutations |
title_sort | limited evolutionary conservation of the phenotypic effects of antibiotic resistance mutations |
topic | Fast Track |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657729/ https://www.ncbi.nlm.nih.gov/pubmed/31058961 http://dx.doi.org/10.1093/molbev/msz109 |
work_keys_str_mv | AT apjokgabor limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT borossgabor limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT nyergesakos limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT feketegergely limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT lazarviktoria limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT pappbalazs limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT palcsaba limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations AT csorgobalint limitedevolutionaryconservationofthephenotypiceffectsofantibioticresistancemutations |