Evidence map›Paper›PMID 39878530›Full record

ArticlemBio2025

Perturbation of

Luke N Yaeger, David Sychantha, Princeton Luong, Shahrokh Shekarriz, Océane Goncalves, Annamaria Dobrin, Michael R Ranieri, Ryan P Lamers, Hanjeong Harvey, George C diCenzo and 4 more

Abstract read
In one paragraph

Article in mBio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Rapid detection ofFrontiers in chemistry · 2025
    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

14 authors.

Luke N YaegerDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0001-8179-8330
David SychanthaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Princeton LuongDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Shahrokh ShekarrizDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Océane GoncalvesDépartement de Biologie, Université de Sherbrooke, Sherbrooke, Québec, Canada.
Annamaria DobrinDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Michael R RanieriDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Ryan P LamersDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Hanjeong HarveyDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
George C diCenzoDepartment of Biology, Queen's University, Kingston, Ontario, Canada.ORCID 0000-0003-3889-6570
Michael SuretteDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0003-0086-4995
Jean-Phiippe CôtéDépartement de Biologie, Université de Sherbrooke, Sherbrooke, Québec, Canada.
Jakob MagolanDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Lori L BurrowsDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0003-0838-5040

Funding

Canadian Government | Natural Sciences and Engineering Research Council of Canada (NSERC) PGS-DCanadian Government | Natural Sciences and Engineering Research Council of Canada (NSERC) RGPIN-2021-04237FRQ | Fonds de Recherche du Québec - Santé (FRQS) Chercheur Boursier Junior 1 FellowshipOntario Research Foundation (ORF) ORF-RE09-047
6 · The paper itself

Abstract

Peptidoglycan (PG) is an important bacterial macromolecule that confers cell shape and structural integrity, and is a key antibiotic target. Its synthesis and turnover are carefully coordinated with other cellular processes and pathways. Despite established connections between the biosynthesis of PG and the outer membrane, or PG and DNA replication, links between PG and folate metabolism remain comparatively unexplored. Folate is an essential cofactor for bacterial growth and is required for the synthesis of many important metabolites. Here we show that inhibition of folate synthesis in the important Gram-negative pathogen IMPORTANCE: To combat the alarming global increase in superbugs amid the simultaneous scarcity of new drugs, we can create synergistic combinations of currently available antibiotics or chimeric molecules with dual activities, to minimize resistance. Here we show that older anti-folate drugs synergize with specific cell wall biosynthesis inhibitors to kill the priority pathogen,

Indexed as

Anti-Bacterial AgentsFolic AcidPeptidoglycanPseudomonas aeruginosaBacterial Proteinsbeta-Lactamasesbeta-LactamsDrug SynergismFosfomycinAmpC beta-lactamasesAnti-Bacterial AgentsBacterial Proteinsbeta-Lactamasesbeta-LactamsFolic AcidFosfomycinPeptidoglycanantibiotic combinationsantibiotic resistancebeta-lactamasecell wallchemical biologyEscherichia colifolatemetallo-beta-lactamasePseudomonas aeruginosapurinessynergy

Identifiers

PMID39878530
PMCPMC11898565

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.