Evidence map›Paper›PMID 26910612›Full record

ArticleFuture medicinal chemistry2016

NH125 kills methicillin-resistant Staphylococcus aureus persisters by lipid bilayer disruption.

Wooseong Kim, Nico Fricke, Annie L Conery, Beth Burgwyn Fuchs, Rajmohan Rajamuthiah, Elamparithi Jayamani, Petia M Vlahovska, Frederick M Ausubel, Eleftherios Mylonakis

Abstract read
In one paragraph

Article in Future medicinal chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.0field-weighted citation impact, top 7% of its field
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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Fighting Antimicrobial Resistance: Innovative Drugs in Antibacterial Research.Angewandte Chemie (International ed. in English) · 2025
    Review
  5. Article
  6. Bacterial persisters: molecular mechanisms and therapeutic development.Signal transduction and targeted therapy · 2024
    Review
  7. Crosstalk involving two-component systems inJournal of bacteriology · 2024
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Frontiers in cellular and infection microbiology · 2022
    Article
  13. Article
  14. Eradication ofFrontiers in microbiology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Phenazine Antibiotic-Inspired Discovery of Bacterial Biofilm-Eradicating Agents.Chembiochem : a European journal of chemical biology · 2019
    Review
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

9 authors at 4 institutions in 1 country.

Wooseong KimDivision of Infectious Diseases, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.
Nico FrickeSchool of Engineering, Brown University, Providence, RI, USA.
Annie L ConeryDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.
Beth Burgwyn FuchsDivision of Infectious Diseases, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.
Rajmohan RajamuthiahDivision of Infectious Diseases, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.
Elamparithi JayamaniDivision of Infectious Diseases, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.
Petia M VlahovskaSchool of Engineering, Brown University, Providence, RI, USA.
Frederick M AusubelDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.
Eleftherios MylonakisDivision of Infectious Diseases, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI, USA.
Rhode Island Hospital · USBrown University · USHarvard University · USMassachusetts General Hospital · US

Funding

Technical Mother Machine CoreP01AI083214 · NIAID · SCHEPENS EYE RESEARCH INSTITUTE · PI Michael S Gilmore · 2009 to 2026
$39.4M
NIAID NIH HHS P01 AI083214
6 · The paper itself

Abstract

backgroundNH125, a known WalK inhibitor kills MRSA persisters. However, its precise mode of action is still unknown. METHODS &

resultsThe mode of action of NH125 was investigated by comparing its spectrum of antimicrobial activity and its effects on membrane permeability and giant unilamellar vesicles (GUVs) with walrycin B, a WalR inhibitor and benzyldimethylhexadecylammonium chloride (16-BAC), a cationic surfactant. NH125 killed persister cells of a variety of Staphylococcus aureus strains. Similar to 16-BAC, NH125 killed MRSA persisters by inducing rapid membrane permeabilization and caused the rupture of GUVs, whereas walrycin B did not kill MRSA persisters or induce membrane permeabilization and did not affect GUVs.

conclusionNH125 kills MRSA persisters by interacting with and disrupting membranes in a detergent-like manner.

Indexed as

Anti-Bacterial AgentsCell Membrane PermeabilityDose-Response Relationship, DrugImidazolesLipid BilayersMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular StructureStructure-Activity RelationshipAnti-Bacterial AgentsImidazolesLipid BilayersNH 125antibioticsgiant unilamellar vesicleMRSANH125two-component system

Identifiers

PMID26910612
PMCPMC4976882
OpenAlexW2276760947

What OpenQuestion holds

Textmetadata
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.