Evidence map›Paper›PMID 39565111›Full record

ArticlemBio2024

Antibiotic resistant bacteria survive treatment by doubling while shrinking.

Adrian Campey, Urszula Łapińska, Remy Chait, Krasimira Tsaneva-Atanasova, Stefano Pagliara

Abstract read
In one paragraph

Article in mBio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Preparing a Dual-SpeciesMolecular pharmaceutics · 2025
    Article
  6. 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
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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.

Adrian CampeyLiving Systems Institute and Biosciences, University of Exeter, Exeter, Devon, United Kingdom.
Urszula ŁapińskaLiving Systems Institute and Biosciences, University of Exeter, Exeter, Devon, United Kingdom.
Remy ChaitLiving Systems Institute and Biosciences, University of Exeter, Exeter, Devon, United Kingdom.
Krasimira Tsaneva-AtanasovaLiving Systems Institute and Biosciences, University of Exeter, Exeter, Devon, United Kingdom.
Stefano PagliaraLiving Systems Institute and Biosciences, University of Exeter, Exeter, Devon, United Kingdom.ORCID 0000-0001-9796-1956

Funding

UKRI | Biotechnology and Biological Sciences Research Council (BBSRC) BB/V008021/1UKRI | Engineering and Physical Sciences Research Council (EPSRC) EP/T017856/1UKRI | Engineering and Physical Sciences Research Council (EPSRC) EP/Y023528/1UKRI | Medical Research Council (MRC) MR/Y033892/1
6 · The paper itself

Abstract

Many antibiotics that are used in healthcare, farming, and aquaculture end up in environments with different spatial structures that might promote heterogeneity in the emergence of antibiotic resistance. However, the experimental evolution of microbes at sub-inhibitory concentrations of antibiotics has been mainly carried out at the population level which does not allow capturing single-cell responses to antibiotics. Here, we investigate and compare the emergence of resistance to ciprofloxacin in IMPORTANCE: The evolution of antimicrobial resistance poses a pressing challenge to global health with an estimated 5 million deaths associated with antimicrobial resistance every year globally. Here, we investigate the diversity of strategies employed by bacteria to survive antibiotics. We discovered that bacteria evolve genetic resistance to antibiotics while simultaneously displaying tolerance to very high doses of antibiotics by doubling while shrinking in size.

Indexed as

Anti-Bacterial AgentsCiprofloxacinEscherichia coliMutationDrug Resistance, BacterialMicrobial Sensitivity TestsMicrobial ViabilityAnti-Bacterial AgentsCiprofloxacinantibiotic toleranceantimicrobial resistanceeffluxenvironmental structureevolutionmicrofluidicsmutationspersisterssequencingsingle-cell analysis

Identifiers

PMID39565111
PMCPMC11633386

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.