Evidence map›Paper›PMID 42860392›Full record

ArticleNature communications2026

Deep learning recognises antibiotic modes of action from brightfield images.

Daniel Krentzel, Kelvin Kho, Julienne Petit, Nassim Mahtal, Thomas Delerue, Max E Huber, Agnès Zettor, Jeanne Chiaravalli, Spencer L Shorte, Mark Brönstrup and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Daniel Krentzel *Imaging and Modeling Unit, Institut Pasteur, Université Paris Cité, Paris, France. daniel.krentzel@pasteur.fr.ORCID 0000-0002-6234-7259
Kelvin Kho *Unité de Biologie et Génétique de la Paroi Bactérienne, CNRS UMR6047, INSERM U1306, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0002-4245-9675
Julienne Petit *Structural Microbiology Unit, CNRS UMR 3528, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0002-2312-4044
Nassim MahtalPhotonic Bio-Imaging, Centre de Ressources et Recherches Technologiques (UTechS-PBI, C2RT), Institut Pasteur, Université Paris Cité, Paris, France.
Thomas DelerueUnité de Biologie et Génétique de la Paroi Bactérienne, CNRS UMR6047, INSERM U1306, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0002-8900-247X
Max E HuberChemical Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0003-3042-0463
Agnès ZettorChemogenomic and Biological Screening Core Facility, CNRS UMR 3523, C2RT, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0002-0592-1963
Jeanne ChiaravalliChemogenomic and Biological Screening Core Facility, CNRS UMR 3523, C2RT, Institut Pasteur, Université Paris Cité, Paris, France.
Spencer L ShortePhotonic Bio-Imaging, Centre de Ressources et Recherches Technologiques (UTechS-PBI, C2RT), Institut Pasteur, Université Paris Cité, Paris, France.
Mark BrönstrupChemical Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0002-8971-7045
Anne Marie WehenkelBacterial Cell Cycle Mechanisms Unit, CNRS UMR 3528, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0003-2327-6512
Ivo G BonecaUnité de Biologie et Génétique de la Paroi Bactérienne, CNRS UMR6047, INSERM U1306, Institut Pasteur, Université Paris Cité, Paris, France. ivo.gomperts-boneca@pasteur.fr.ORCID 0000-0001-8122-509X
Christophe ZimmerImaging and Modeling Unit, Institut Pasteur, Université Paris Cité, Paris, France. christophe.zimmer@uni-wuerzburg.de.ORCID 0000-0001-9910-1589

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-16-CONV-0005Fondation pour la Recherche Médicale (Foundation for Medical Research in France) FDT202404018132
6 · The paper itself

Abstract

The antimicrobial resistance crisis urgently calls for antibiotics with novel modes of action (MoAs). While growth inhibition assays can identify antibiotic molecules, they miss promising compounds below inhibitory concentrations and cannot reveal their MoA. Imaging-based profiling of drug-treated bacteria can inform on MoA, but current approaches generally require fluorescent labelling and/or inhibitory concentrations and it remains unclear whether compounds with novel MoAs can be robustly detected. Here, we demonstrate a deep learning approach to recognise antibiotic MoAs from unlabelled images. We train a convolutional neural network to predict treatment conditions from brightfield images of Escherichia coli exposed to antibiotics covering eight MoAs. Our approach can detect drug exposure at subinhibitory concentrations and allows near-perfect MoA recognition, even when trained on only eight images per treatment condition. Previously unseen compounds are assigned to their correct MoA with good accuracy if the MoA is represented in the training data, and our method can robustly detect MoA novelty in five out of six considered MoAs, enabling microscopy-based identification of new antibiotic classes. We also achieve near-perfect MoA recognition in Klebsiella pneumoniae, suggesting applicability to other species. Our approach complements growth inhibition assays and is poised to improve the search for innovative antibiotic compounds.

Indexed as

Anti-Bacterial AgentsDeep LearningEscherichia coliConvolutional Neural NetworksImage Processing, Computer-AssistedMicrobial Sensitivity TestsAnti-Bacterial Agents

Identifiers

PMID42860392
PMCPMC13655182

What OpenQuestion holds

Textmetadata
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.