Evidence map›Paper›PMID 40011610›Full record

ArticleCommunications biology2025

Ribosome phenotypes for rapid classification of antibiotic-susceptible and resistant strains of Escherichia coli.

Alison Farrar, Piers Turner, Hafez El Sayyed, Conor Feehily, Stelios Chatzimichail, Sammi Ta, Derrick Crook, Monique Andersson, Sarah Oakley, Lucinda Barrett and 3 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

13 authors.

Alison FarrarDepartment of Physics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-6849-3353
Piers TurnerDepartment of Physics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-3644-0636
Hafez El SayyedDepartment of Physics, University of Oxford, Oxford, UK.
Conor FeehilySchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Stelios ChatzimichailDepartment of Physics, University of Oxford, Oxford, UK.
Sammi TaDepartment of Physics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0009-0000-9912-9805
Derrick CrookNuffield Department of Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Monique AnderssonDepartment of Microbiology and Infectious Diseases, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Sarah OakleyDepartment of Microbiology and Infectious Diseases, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Lucinda BarrettDepartment of Microbiology and Infectious Diseases, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Christoffer NellåkerNuffield Department of Women's & Reproductive Health, University of Oxford, Big Data Institute, Oxford, UK.ORCID http://orcid.org/0000-0002-2887-2068
Nicole StoesserNuffield Department of Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.ORCID http://orcid.org/0000-0002-4508-7969
Achillefs KapanidisDepartment of Physics, University of Oxford, Oxford, UK. kapanidis@physics.ox.ac.uk.ORCID http://orcid.org/0000-0001-6699-136X

Funding

RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/N018656/1RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/S008896/1Wellcome TrustWellcome Trust (Wellcome) 110164/Z/15/Z
6 · The paper itself

Abstract

Rapid antibiotic susceptibility tests (ASTs) are an increasingly important part of clinical care as antimicrobial resistance (AMR) becomes more common in bacterial infections. Here, we use the spatial distribution of fluorescently labelled ribosomes to detect intracellular changes associated with antibiotic susceptibility in E. coli cells using a convolutional neural network (CNN). By using ribosome-targeting probes, one fluorescence image provides data for cell segmentation and susceptibility phenotyping. Using 60,382 cells from an antibiotic-susceptible laboratory strain of E. coli, we showed that antibiotics with different mechanisms of action result in distinct ribosome phenotypes, which can be identified by a CNN with high accuracy (99%, 98%, 95%, and 99% for ciprofloxacin, gentamicin, chloramphenicol, and carbenicillin). With 6 E. coli strains isolated from bloodstream infections, we used 34,205 images of ribosome phenotypes to train a CNN that could classify susceptible cells with 91% accuracy and resistant cells with 99% accuracy. Such accuracies correspond to the ability to differentiate susceptible and resistant samples with 99% confidence with just 2 cells, meaning that this method could eliminate lengthy culturing steps and could determine susceptibility with 30 min of antibiotic treatment. The ribosome phenotype method should also be able to identify phenotypes in other strains and species.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialEscherichia coliRibosomesMicrobial Sensitivity TestsNeural Networks, ComputerPhenotypeAnti-Bacterial Agents

Identifiers

PMID40011610
PMCPMC11865533

What OpenQuestion holds

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Registered trials

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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.