Evidence map›Paper›PMID 42168581›Full record

ArticleCommunications biology2026

Deep-learning deconvolution and segmentation of fluorescent membranes for high-precision bacterial cell-size profiling.

Octavio Reyes-Matte, Carsten Fortmann-Grote, Beate Gericke, Nadja Hüttmann, Nikola Ojkic, Javier López-Garrido

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Octavio Reyes-MatteMax Planck Institute for Evolutionary Biology, Plön, Germany. reyesmatte@evolbio.mpg.de.ORCID 0009-0006-7031-6213
Carsten Fortmann-GroteMax Planck Institute for Evolutionary Biology, Plön, Germany.
Beate GerickeMax Planck Institute for Evolutionary Biology, Plön, Germany.
Nadja HüttmannMax Planck Institute for Evolutionary Biology, Plön, Germany.
Nikola OjkicSchool of Biological and Behavioral Sciences, Queen Mary University of London, London, UK.
Javier López-GarridoMax Planck Institute for Evolutionary Biology, Plön, Germany. lopezgarrido@evolbio.mpg.de.ORCID 0000-0002-8907-502X

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 853323RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/Y009002/1
6 · The paper itself

Abstract

Evolutionary studies in bacteria have emphasized genetic and metabolic diversity, while cell-size variation has received less attention. Here we introduce MEDUSSA, a high-throughput method for precise bacterial cell-size profiling based on automatic segmentation of fluorescent membrane images, well suited to studying cell-size diversity. The approach uses deep-learning-based membrane deconvolution, segmentation models fine-tuned for fluorescent-membrane images, and error-corrected cell measurement to extract accurate sizes from individual bacterial cells regardless of shape, size, chaining, or clustering. Our method overcomes limitations of phase-contrast segmentation, yielding reliable single-cell dimensions. We applied MEDUSSA to six strains of Priestia megaterium and found over twofold differences in cell volume across strains, largely driven by differences in cell width. We identified a partially-functional PBP1 allele that underlies the reduced width of one strain. Together, these results demonstrate the power of comparative analyses in bacterial cell biology and expand the toolkit to investigate the evolution of bacterial cell size.

Indexed as

Cell MembraneDeep LearningImage Processing, Computer-AssistedCell Size

Identifiers

PMID42168581
PMCPMC13194920

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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.