Evidence map›Paper›PMID 26446807›Full record

ArticleProceedings. Biological sciences2015

The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic.

Clara Torres-Barceló, Mila Kojadinovic, Richard Moxon, R Craig MacLean

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings. Biological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. The Role of the SOS Response in the Adaptation ofCurrent issues in molecular biology · 2026
    Review
  3. Phage provoke growth delays and SOS response induction despite CRISPR-Cas protection.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  4. Insights into antibiotic resistance promoted by quinolone exposure.Antimicrobial agents and chemotherapy · 2025
    Article
  5. Evolution takes multiple paths to evolvability when facing environmental change.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Antibacterial Mechanisms and Clinical Impact of Sitafloxacin.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. NaturalizedFrontiers in microbiology · 2022
    Review
  13. Article
  14. Sub-Inhibitory Antibiotic Exposure and Virulence inAntibiotics (Basel, Switzerland) · 2021
    Review
  15. Risk Factors for and Mechanisms ofOpen forum infectious diseases · 2021
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Clara Torres-BarcelóDepartment of Zoology, University of Oxford, Oxford OX1 3PS, UK Institut des Sciences de l'Evolution, CNRS-Université Montpellier 2, Montpellier, France clara.torres@univ-montp2.fr.
Mila KojadinovicDepartment of Zoology, University of Oxford, Oxford OX1 3PS, UK.
Richard MoxonUniversity of Oxford Medical Sciences Division, John Radcliffe Hospital, Oxford OX3 9DS, UK.
R Craig MacLeanDepartment of Zoology, University of Oxford, Oxford OX1 3PS, UK.
University of Oxford · GBJohn Radcliffe Hospital · GB

Funding

European Research Council 281591
6 · The paper itself

Abstract

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.

Indexed as

Biological EvolutionGenetic FitnessAnti-Bacterial AgentsCiprofloxacinDrug Resistance, BacterialGene Expression Regulation, BacterialPseudomonas aeruginosaSOS Response, GeneticsAnti-Bacterial AgentsCiprofloxacinantibioticsbacteriaevolvabilityfitnessSOS responsestress

Identifiers

PMID26446807
PMCPMC4614765
OpenAlexW2416484602

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.