Evidence map›Paper›PMID 39966225›Full record

ArticleProbiotics and antimicrobial proteins2025

Characterization of agr-like Loci in Lactiplantibacillus plantarum and L. paraplantarum and Their Role in Quorum Sensing and Virulence Inhibition of Staphylococcus aureus.

Weizhe Wang, Ifigeneia Kyrkou, Martin S Bojer, Dina Kalloubi, Abdul Jabbar Kali, Miguel Alena-Rodriguez, Jørgen J Leisner, Stephanie Fulaz, Hanne Ingmer

Abstract read
In one paragraph

Article in Probiotics and antimicrobial proteins, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Tetrathionate sensing enablesGut microbes · 2026
    Article
  2. Review
  3. Strategic antagonism: howFrontiers in microbiology · 2025
    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.

Weizhe WangBacterial & Viruses Section, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, 1870, Copenhagen, Denmark.
Ifigeneia KyrkouBacterial & Viruses Section, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, 1870, Copenhagen, Denmark.
Martin S BojerBacterial & Viruses Section, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, 1870, Copenhagen, Denmark.
Dina KalloubiCenter for Biopharmaceuticals & Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Denmark.
Abdul Jabbar KaliCenter for Biopharmaceuticals & Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Denmark.
Miguel Alena-RodriguezCenter for Biopharmaceuticals & Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Jagtvej 160, 2100, Copenhagen, Denmark.
Jørgen J LeisnerBacterial & Viruses Section, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, 1870, Copenhagen, Denmark.
Stephanie FulazBacterial & Viruses Section, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, 1870, Copenhagen, Denmark. stephanie.silva@sund.ku.dk.
Hanne IngmerBacterial & Viruses Section, Department of Veterinary and Animal Sciences, University of Copenhagen, Stigbøjlen 4, 1870, Copenhagen, Denmark. hi@sund.ku.dk.

Funding

LEO Fondet LF-OC-20-000517Novo Nordisk Fonden NNF22OC0077593
6 · The paper itself

Abstract

The pathogenicity of Staphylococcus aureus is largely regulated by the agr quorum sensing (QS) system encoded by agrBDCA, which coordinates virulence factor production through secretion and sensing of auto-inducing peptides (AIPs). agr-like systems are also present in coagulase-negative staphylococci, and several of these encode AIPs that inhibit S. aureus QS. In lactic acid bacteria, a similar locus was previously identified in Lactiplantibacillus plantarum WCSF1 termed lamBDCA. Here, we characterized the lamBDCA locus in L. plantarum LMG 13556 and L. paraplantarum CIRM-BIA 1870, and explored the effects on S. aureus QS. Notably, we found that co-cultivation with L. paraplantarum significantly inhibits S. aureus QS and hemolysin production, while less so for L. plantarum. The inhibition by L. paraplantarum was lost upon disruption of its lamBDCA locus, suggesting that the L. paraplantarum AIP mediates cross-species interference with S. aureus agr activation. Transcriptomic analysis revealed that lamBDCA in L. paraplantarum controls the expression of genes belonging to various functional categories, including stress response and metabolism. The latter includes genes encoding riboflavin (B2 vitamin) biosynthesis, which enabled the growth of the L. paraplantarum lamB mutant in the presence of roseoflavin, a toxic riboflavin analogue. Collectively, our results show that L. paraplantarum CIRM-BIA 1870 interferes with S. aureus virulence gene expression through QS suppression, and they implicate QS in the probiotic properties of L. paraplantarum.

Indexed as

Bacterial ProteinsLactiplantibacillus plantarumLactobacillaceaeQuorum SensingStaphylococcus aureusGene Expression Regulation, BacterialTrans-ActivatorsVirulenceVirulence FactorsAgr protein, Staphylococcus aureusBacterial ProteinsTrans-ActivatorsVirulence Factorsagr systemAnti-virulence therapyAuto-inducing peptides (AIPs)Cross-species communicationProbioticsQuorum sensing

Identifiers

PMID39966225
PMCPMC12405376

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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.