Evidence map›Paper›PMID 41674902›Full record

ArticleFrontiers in microbiology2025

Multifaceted antimicrobial mechanisms of NCR147-derived peptides from

Hilda Tiricz, Rui M Lima, Ilona Pfeiffer, Nóra Igaz, Ildikó Domonkos, Sándor Jenei, Dian H O Howan, Alexandra Pál, Edit Tímár, Éva Hunyadi-Gulyás and 3 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2025. 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
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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

13 authors.

Hilda TiriczInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.
Rui M LimaInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.
Ilona PfeifferDepartment of Biotechnology and Microbiology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
Nóra IgazDepartment of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
Ildikó DomonkosInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.
Sándor JeneiInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.
Dian H O HowanDepartment of Medical Chemistry, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Alexandra PálInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.
Edit TímárInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.
Éva Hunyadi-GulyásProteomics Research Group, Core Facility, HUN-REN Biological Research Centre, Szeged, Hungary.
Gábor K TóthDepartment of Medical Chemistry, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Zoltán BozsóPlant Protection Institute, HUN-REN Centre for Agricultural Research, Budapest, Hungary.
Éva KondorosiInstitute of Plant Biology, HUN-REN Biological Research Centre, Szeged, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Antimicrobial peptides (AMPs), key components of innate immunity, offer broad-spectrum activity against diverse pathogens. In Materials and methods: In this study, 13 truncated and substituted derivatives of NCR147 were chemically synthesized to identify peptide regions responsible for antimicrobial activity. Antimicrobial efficacy was evaluated against 18 pathogens by determining minimum bactericidal and minimum fungicidal concentrations. Inhibition and eradication of bacterial biofilms were assessed to determine peptide effects. Cytotoxicity was measured using hemolysis assays and multiple viability assays in human cell cultures. Peptide interactions with membrane lipids, effects on membrane permeability, and modulation of bacterial efflux pumps were analyzed using established biochemical and biophysical assays. Bacterial proteins interacting with selected peptides were identified by affinity chromatography followed by LC-MS/MS. Results: The NCR147 derivatives displayed varying degrees of antimicrobial potency and spectrum. Analysis of the physicochemical properties and predicted 3D structures of 13 NCR peptide variants revealed that the antimicrobial region resides in the C-terminal portion of these intrinsically disordered peptides, where the WAW hydrophobic patch together with the positively charged amino acids contribute to antimicrobial activity, most likely through interactions with microbial membranes. The most active peptides provoked alteration of bacterial membranes, inhibited efflux pumps, and interfered with essential intracellular targets. Moreover, these peptides exhibited potent antibiofilm effects, including the ability to both prevent and degrade Discussion: These findings reveal that NCR147-derived peptides function via a multihit mechanism and highlight the therapeutic promise of plant-derived AMPs as next-generation antimicrobials with reduced risk of resistance development.

Indexed as

antimicrobial activitybacterial targetsbiofilm inhibitionCandida albicansCryptococcus neoformansefflux pump inhibitionESKAPE bacteria

Identifiers

PMID41674902
PMCPMC12886489

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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.