Evidence map›Paper›PMID 41860239›Full record

ArticlemSystems2026

Findlay D Munro, Elize Ambulte, Claudia M Hemsley, Megan Bergkessel

Abstract read
In one paragraph

Article in mSystems, 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

4 authors.

Findlay D MunroDivision of Molecular Microbiology, University of Dundee School of Life Sciences, Dundee, United Kingdom.ORCID 0000-0003-4164-1544
Elize AmbulteDivision of Molecular Microbiology, University of Dundee School of Life Sciences, Dundee, United Kingdom.
Claudia M HemsleyDivision of Molecular Microbiology, University of Dundee School of Life Sciences, Dundee, United Kingdom.
Megan BergkesselDivision of Molecular Microbiology, University of Dundee School of Life Sciences, Dundee, United Kingdom.ORCID 0000-0002-4530-1224

Funding

Academy of Medical Sciences SBF005/1096Medical Research Council MR/T041811/1, MR/Z000378/1Wellcome TrustWellcome Trust 204816/Z/16/Z,218520/Z/19/Z
6 · The paper itself

Abstract

Heterotrophic bacteria rapidly deplete essential macronutrients during growth and must navigate subsequent periods of growth arrest imposed by starvation. Nutrient limitations can be dynamic in nature, requiring ongoing regulatory adjustments involving new protein synthesis despite total biosynthetic activities being dramatically lower than during growth. Here, we have characterized the responses of the opportunistic pathogen IMPORTANCE: Molecular microbiology has traditionally focused on exponential growth in model organisms as the preferred context in which to study bacterial physiology, especially the regulation of new protein synthesis. However, in natural environments, including many infection contexts, bacteria frequently enter growth arrest due to nutrient limitation. The dynamics and regulation of protein synthesis in growth-arrested cells remain poorly understood, especially in pathogens. Furthermore, growth arrest increases tolerance to a variety of stresses, including many clinically used antimicrobials. We have conducted a comprehensive exploration of the proteins being made by growth arrested

Indexed as

Pseudomonas aeruginosaBacterial ProteinsCarbonGene Expression Regulation, BacterialNitrogenProtein BiosynthesisProteomeProteomicsBacterial ProteinsCarbonNitrogenProteomeBONCATcarbon starvationmicrobial dormancynitrogen starvationproteomicsPseudomonas aeruginosaTn-Seq

Identifiers

PMID41860239
PMCPMC13098243

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.