Evidence map›Paper›PMID 25689336›Full record

ReviewNature chemical biology2015

Collective antibiotic tolerance: mechanisms, dynamics and intervention.

Hannah R Meredith, Jaydeep K Srimani, Anna J Lee, Allison J Lopatkin, Lingchong You

Abstract readReview
In one paragraph

Review in Nature chemical biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
–field-weighted citation impact
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

87 citing papers in PubMed.

  1. Article
  2. Article
  3. Pyocyanin produced byAntimicrobial agents and chemotherapy · 2026
    Article
  4. Contributions of intra- and extracellular antibiotic degradation to collective [Formula: see text]-lactam survival.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Challenges and opportunities in the management of severe pneumonia. Key concepts from the Seventh Annual Meeting of Spanish Experts 2025.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Spatial population dynamics of bacterial colonies with social antibiotic resistance.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Article
  16. Habitat fragmentation enhances microbial collective defence.Journal of the Royal Society, Interface · 2025
    Article
  17. Review
  18. Article
  19. Article
  20. Article

27 more citing papers are in PubMed but not listed here.

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

5 authors.

Hannah R MeredithDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Jaydeep K SrimaniDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Anna J LeeDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Allison J LopatkinDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Lingchong You1] Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA. [2] Center for Systems Biology, Duke University, Durham, North Carolina, USA. [3] Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, USA.

Funding

Post-antibiotic effect and design of optimal antibiotic dosing protocolsR01GM098642 · NIGMS · DUKE UNIVERSITY · PI YOU, LINGCHONG · 2011 to 2025
$3.6M
A synthetic biology approach to analyze evolution of programmed bacterial deathR01GM110494 · NIGMS · DUKE UNIVERSITY · PI YOU, LINGCHONG · 2014 to 2017
$1.2M
NIGMS NIH HHS R01 GM098642NIGMS NIH HHS R01 GM110494
6 · The paper itself

Abstract

Bacteria have developed resistance against every antibiotic at a rate that is alarming considering the timescale at which new antibiotics are developed. Thus, there is a critical need to use antibiotics more effectively, extend the shelf life of existing antibiotics and minimize their side effects. This requires understanding the mechanisms underlying bacterial drug responses. Past studies have focused on survival in the presence of antibiotics by individual cells, as genetic mutants or persisters. Also important, however, is the fact that a population of bacterial cells can collectively survive antibiotic treatments lethal to individual cells. This tolerance can arise by diverse mechanisms, including resistance-conferring enzyme production, titration-mediated bistable growth inhibition, swarming and interpopulation interactions. These strategies can enable rapid population recovery after antibiotic treatment and provide a time window during which otherwise susceptible bacteria can acquire inheritable genetic resistance. Here, we emphasize the potential for targeting collective antibiotic tolerance behaviors as an antibacterial treatment strategy.

Indexed as

AnimalsAnti-Bacterial AgentsBacteriaBacterial InfectionsDrug Resistance, BacterialHumansAnti-Bacterial Agents

Identifiers

PMID25689336
PMCPMC4806783

What OpenQuestion holds

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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.