Evidence map›Paper›PMID 41775806›Full record

Articlenpj antimicrobials and resistance2026

Novel continuous experimental evolution methodology uncovers rapid resistance development and cross-resistance.

Thaddäus Echelmeyer, Markus Ellmann, Stefan E Heiden, Kaan Kocer, Michael Schwabe, Helmut Fickenscher, Gregor Maschkowitz, Sebastian Guenther, Dennis Nurjadi, Katharina Schaufler and 1 more

Abstract read
In one paragraph

Article in npj antimicrobials and resistance, 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

11 authors.

Thaddäus EchelmeyerDepartment of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research, Greifswald, Germany.
Markus EllmannDepartment of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research, Greifswald, Germany.
Stefan E HeidenDepartment of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research, Greifswald, Germany.
Kaan KocerInstitute of Medical Microbiology, University of Lübeck and University Medical Center Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Michael SchwabeDepartment of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research, Greifswald, Germany.
Helmut FickenscherInstitute of Medical Microbiology, Christian-Albrecht University Kiel and University Medical Center Schleswig-Holstein, Kiel, Germany.
Gregor MaschkowitzInstitute of Medical Microbiology, Christian-Albrecht University Kiel and University Medical Center Schleswig-Holstein, Kiel, Germany.
Sebastian GuentherPharmaceutical Biology, Institute of Pharmacy, University of Greifswald, Greifswald, Germany.
Dennis NurjadiInstitute of Medical Microbiology, University of Lübeck and University Medical Center Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Katharina Schaufler *Department of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research, Greifswald, Germany.
Elias Eger *Department of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research, Greifswald, Germany. elias.eger@helmholtz-hioh.de.

Funding

Bundesministerium für Forschung und Technologie 01KI2410
6 · The paper itself

Abstract

Antimicrobial resistance poses a significant global health threat. Experimental evolution studies are crucial in understanding resistance mechanisms and thereby informing strategies to preserve antibiotic efficacy. We developed a novel continuous experimental evolution system enabling uninterrupted medium exchange with a rising antibiotic gradient, using standard laboratory equipment. We applied this system to three Enterobacter cloacae complex strains isolated from urinary tract infections in Germany between 1990 and 1992, which therefore had no prior exposure to cefepime, a fourth-generation cephalosporin approved in Germany in 2004. After four days of exposure to a cefepime gradient, resistant mutants emerged in all three strains. Notably, one mutant exhibited cross-resistance to the novel antibiotics cefiderocol and ceftazidime-avibactam, due to a single missense mutation in the β-lactamase gene bla

Identifiers

PMID41775806
PMCPMC12957303

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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.