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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...

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Autores principales: Torres-Barceló, Clara, Kojadinovic, Mila, Moxon, Richard, MacLean, R. Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2015
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.
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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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