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The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic
Exposure to antibiotics induces the expression of mutagenic bacterial stress–response pathways, but the evolutionary benefits of these responses remain unclear. One possibility is that stress–response pathways provide a short-term advantage by protecting bacteria against the toxic effects of antibio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614765/ https://www.ncbi.nlm.nih.gov/pubmed/26446807 http://dx.doi.org/10.1098/rspb.2015.0885 |
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author | Torres-Barceló, Clara Kojadinovic, Mila Moxon, Richard MacLean, R. Craig |
author_facet | Torres-Barceló, Clara Kojadinovic, Mila Moxon, Richard MacLean, R. Craig |
author_sort | Torres-Barceló, Clara |
collection | PubMed |
description | Exposure to antibiotics induces the expression of mutagenic bacterial stress–response pathways, but the evolutionary benefits of these responses remain unclear. One possibility is that stress–response pathways provide a short-term advantage by protecting bacteria against the toxic effects of antibiotics. Second, it is possible that stress-induced mutagenesis provides a long-term advantage by accelerating the evolution of resistance. Here, we directly measure the contribution of the Pseudomonas aeruginosa SOS pathway to bacterial fitness and evolvability in the presence of sublethal doses of ciprofloxacin. Using short-term competition experiments, we demonstrate that the SOS pathway increases competitive fitness in the presence of ciprofloxacin. Continued exposure to ciprofloxacin results in the rapid evolution of increased fitness and antibiotic resistance, but we find no evidence that SOS-induced mutagenesis accelerates the rate of adaptation to ciprofloxacin during a 200 generation selection experiment. Intriguingly, we find that the expression of the SOS pathway decreases during adaptation to ciprofloxacin, and this helps to explain why this pathway does not increase long-term evolvability. Furthermore, we argue that the SOS pathway fails to accelerate adaptation to ciprofloxacin because the modest increase in the mutation rate associated with SOS mutagenesis is offset by a decrease in the effective strength of selection for increased resistance at a population level. Our findings suggest that the primary evolutionary benefit of the SOS response is to increase bacterial competitive ability, and that stress-induced mutagenesis is an unwanted side effect, and not a selected attribute, of this pathway. |
format | Online Article Text |
id | pubmed-4614765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-46147652015-11-02 The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic Torres-Barceló, Clara Kojadinovic, Mila Moxon, Richard MacLean, R. Craig Proc Biol Sci Research Articles Exposure to antibiotics induces the expression of mutagenic bacterial stress–response pathways, but the evolutionary benefits of these responses remain unclear. One possibility is that stress–response pathways provide a short-term advantage by protecting bacteria against the toxic effects of antibiotics. Second, it is possible that stress-induced mutagenesis provides a long-term advantage by accelerating the evolution of resistance. Here, we directly measure the contribution of the Pseudomonas aeruginosa SOS pathway to bacterial fitness and evolvability in the presence of sublethal doses of ciprofloxacin. Using short-term competition experiments, we demonstrate that the SOS pathway increases competitive fitness in the presence of ciprofloxacin. Continued exposure to ciprofloxacin results in the rapid evolution of increased fitness and antibiotic resistance, but we find no evidence that SOS-induced mutagenesis accelerates the rate of adaptation to ciprofloxacin during a 200 generation selection experiment. Intriguingly, we find that the expression of the SOS pathway decreases during adaptation to ciprofloxacin, and this helps to explain why this pathway does not increase long-term evolvability. Furthermore, we argue that the SOS pathway fails to accelerate adaptation to ciprofloxacin because the modest increase in the mutation rate associated with SOS mutagenesis is offset by a decrease in the effective strength of selection for increased resistance at a population level. Our findings suggest that the primary evolutionary benefit of the SOS response is to increase bacterial competitive ability, and that stress-induced mutagenesis is an unwanted side effect, and not a selected attribute, of this pathway. The Royal Society 2015-10-07 /pmc/articles/PMC4614765/ /pubmed/26446807 http://dx.doi.org/10.1098/rspb.2015.0885 Text en © 2015 The Authors. http://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/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Torres-Barceló, Clara Kojadinovic, Mila Moxon, Richard MacLean, R. Craig The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
title | The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
title_full | The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
title_fullStr | The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
title_full_unstemmed | The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
title_short | The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
title_sort | sos response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614765/ https://www.ncbi.nlm.nih.gov/pubmed/26446807 http://dx.doi.org/10.1098/rspb.2015.0885 |
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