Evidence map›Paper›PMID 38110697›Full record

ArticleNature microbiology2024

Commensal production of a broad-spectrum and short-lived antimicrobial peptide polyene eliminates nasal Staphylococcus aureus.

Benjamin O Torres Salazar, Taulant Dema, Nadine A Schilling, Daniela Janek, Jan Bornikoel, Anne Berscheid, Ahmed M A Elsherbini, Sophia Krauss, Simon J Jaag, Michael Lämmerhofer and 9 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Nature microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 45 citations in OpenAlex.

  1. Artificial intelligence catalyzes antimicrobial peptide design.Synthetic and systems biotechnology · 2027
    Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. SET-M33 peptide as a selectiveMicrobiology spectrum · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Integration of Postbiotics into Adult Diapers:Life (Basel, Switzerland) · 2025
    Article
  15. Article
  16. Journal of bacteriology · 2025
    Review
  17. Article
  18. Article
  19. Complete genome sequence ofMicrobiology resource announcements · 2025
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 4 countries.

Benjamin O Torres Salazar *Department of Infection Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.
Taulant Dema *Institute of Organic Chemistry, University of Tübingen, Tübingen, Germany.ORCID 0000-0002-1932-2937
Nadine A SchillingCluster of Excellence EXC 2124 Controlling Microbes to Fight Infections, Tübingen, Germany.
Daniela JanekDepartment of Infection Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.
Jan BornikoelDepartment of Microbial Bioactive Compounds, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.ORCID 0000-0002-9198-6025
Anne BerscheidGerman Center for Infection Research (DZIF), partner site Tübingen, Tübingen, Germany.ORCID 0000-0003-1585-8715
Ahmed M A ElsherbiniDepartment of Infection Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.ORCID 0000-0003-0267-4239
Sophia KraussDepartment of Infection Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.
Simon J JaagInstitute of Pharmaceutical Sciences, University of Tübingen, Tübingen, Germany.ORCID 0000-0002-3847-774X
Michael LämmerhoferInstitute of Pharmaceutical Sciences, University of Tübingen, Tübingen, Germany.ORCID 0000-0002-1318-0974
Min LiDepartment of Laboratory Medicine, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Norah AlqahtaniDepartment of Infection Biology and Microbiomes, University of Liverpool, Liverpool, UK.ORCID 0000-0002-8056-5057
Malcolm J HorsburghDepartment of Infection Biology and Microbiomes, University of Liverpool, Liverpool, UK.ORCID 0000-0002-3806-0039
Tilmann WeberThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kongens Lyngby, Denmark.ORCID 0000-0002-8260-5120
José Manuel Beltrán-BeleñaCluster of Excellence EXC 2124 Controlling Microbes to Fight Infections, Tübingen, Germany.ORCID 0000-0002-8553-468X
Heike Brötz-OesterheltGerman Center for Infection Research (DZIF), partner site Tübingen, Tübingen, Germany.ORCID 0000-0001-9364-1832
Stephanie GrondCluster of Excellence EXC 2124 Controlling Microbes to Fight Infections, Tübingen, Germany. stephanie.grond@uni-tuebingen.de.ORCID 0000-0002-7549-4936
Bernhard KrismerDepartment of Infection Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany. b.krismer@uni-tuebingen.de.ORCID 0000-0002-9505-8285
Andreas PeschelDepartment of Infection Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.ORCID 0000-0002-3209-8626
German Center for Infection Research · DEUniversity of Tübingen · DEBG Klinik Tübingen · DEUniversity of Liverpool · GBNovo Nordisk Foundation · DKRenji Hospital · CN

Funding

Biotechnology and Biological Sciences Research Council BB/L024209/1Deutsche Forschungsgemeinschaft (German Research Foundation) Cluster of Excellence EXC2124 Controlling Microbes to Fight Infection; project ID 390838134Deutsche Forschungsgemeinschaft (German Research Foundation) TRR261 (project ID 398967434), GRK1708Deutsche Forschungsgemeinschaft (German Research Foundation) TRR261 (project ID 398967434),GRK1708Deutsche Forschungsgemeinschaft (German Research Foundation) TRR261 (project ID 398967434), TRR156 (project ID 246807620), GRK1708Deutsche Forschungsgemeinschaft (German Research Foundation) ZUK 63Novo Nordisk Fonden (Novo Nordisk Foundation) project ID NNF20CC0035580
6 · The paper itself

Abstract

Antagonistic bacterial interactions often rely on antimicrobial bacteriocins, which attack only a narrow range of target bacteria. However, antimicrobials with broader activity may be advantageous. Here we identify an antimicrobial called epifadin, which is produced by nasal Staphylococcus epidermidis IVK83. It has an unprecedented architecture consisting of a non-ribosomally synthesized peptide, a polyketide component and a terminal modified amino acid moiety. Epifadin combines a wide antimicrobial target spectrum with a short life span of only a few hours. It is highly unstable under in vivo-like conditions, potentially as a means to limit collateral damage of bacterial mutualists. However, Staphylococcus aureus is eliminated by epifadin-producing S. epidermidis during co-cultivation in vitro and in vivo, indicating that epifadin-producing commensals could help prevent nasal S. aureus carriage. These insights into a microbiome-derived, previously unknown antimicrobial compound class suggest that limiting the half-life of an antimicrobial may help to balance its beneficial and detrimental activities.

Indexed as

Anti-Infective AgentsStaphylococcal InfectionsAntimicrobial PeptidesHumansStaphylococcus aureusStaphylococcus epidermidisAnti-Infective AgentsAntimicrobial Peptides

Identifiers

PMID38110697
PMCPMC11310079
OpenAlexW4389894264

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.