Evidence map›Paper›PMID 41231718›Full record

ArticleMicrobiology (Reading, England)2025

Rapid accumulation of fluorophores and fast kill identify drugs with bactericidal effects against Gram-negative bacteria.

J Enrique Salcedo-Sora, Douglas Bruce Kell

Abstract read
In one paragraph

Article in Microbiology (Reading, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

J Enrique Salcedo-SoraGeneMill Research Facility, Liverpool Shared Research Facilities, University of Liverpool, Crown Street, Liverpool, L69 7ZB, UK.
Douglas Bruce KellGeneMill Research Facility, Liverpool Shared Research Facilities, University of Liverpool, Crown Street, Liverpool, L69 7ZB, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial resistance is a massive threat, but developing a new antibiotic can take decades. That time could be drastically reduced if we were able to anticipate desirable properties of a chemical, such as its potential to target specific bacterial compartments. This would provide the opportunity to prioritize the development of molecules that target, for instance, the cell membrane, as this does not rely on transporters and usually results in a fast-acting bactericidal effect. We used flow cytometry and a set of fluorophores together with a group of antibiotics to discriminate between antimicrobials acting on cell membrane versus intracellularly against two Gram-negative bacteria,

Indexed as

AcinetobacterAnti-Bacterial AgentsEscherichia coliFluorescent DyesGram-Negative BacteriaCell MembraneFlow CytometryMicrobial Sensitivity TestsMicrobial ViabilityAnti-Bacterial AgentsFluorescent DyesA. baylyiantibioticscell membraneE. coliflow cytometryfluorophoresGram-negativepolymyxinsPrestwick library

Identifiers

PMID41231718
PMCPMC12614362

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.