Evidence map›Paper›PMID 39379373›Full record

ArticleNature communications2024

PlzR regulates type IV pili assembly in Pseudomonas aeruginosa via PilZ binding.

Hanne Hendrix, Annabel Itterbeek, Hannelore Longin, Lize Delanghe, Eveline Vriens, Marta Vallino, Eveline-Marie Lammens, Farhana Haque, Ahmed Yusuf, Jean-Paul Noben and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A cold-responsiveApplied and environmental microbiology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Understanding phage Receptor-binding protein interaction with host surface receptor: the key for phage-Mediated detection and elimination of Pseudomonas aeruginosa.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. 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.

Hanne HendrixLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Annabel ItterbeekLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Hannelore LonginLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.ORCID 0000-0001-8524-5768
Lize DelangheLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Eveline VriensLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Marta VallinoInstitute for Sustainable Plant Protection, National Research Council of Italy, IPSP-CNR Headquarter, Turin, Italy.
Eveline-Marie LammensLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.ORCID 0000-0002-4946-4469
Farhana HaqueDepartment of Biology, Texas A&M University, College Station, TX, USA.
Ahmed YusufDepartment of Biology, Texas A&M University, College Station, TX, USA.ORCID 0009-0007-0288-526X
Jean-Paul NobenBiomedical Research Institute and Transnational University Limburg, School of Life Sciences, Hasselt University, Diepenbeek, Belgium.
Maarten BoonLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Matthias D KochDepartment of Biology, Texas A&M University, College Station, TX, USA.ORCID 0000-0003-4408-9900
Vera van NoortComputational Systems Biology, Department of Microbial and Molecular Systems, KU Leuven, Heverlee, Belgium.ORCID 0000-0002-8436-6602
Rob LavigneLaboratory of Gene Technology, Department of Biosystems, KU Leuven, Heverlee, Belgium. rob.lavigne@kuleuven.be.ORCID 0000-0001-7377-1314

Funding

KU Leuven (Katholieke Universiteit Leuven) C16/20/001KU Leuven (Katholieke Universiteit Leuven) iBOF/21/092
6 · The paper itself

Abstract

Type IV pili (T4P) are thin, flexible filaments exposed on the cell surface of gram-negative bacteria and are involved in pathogenesis-related processes, including cell adsorption, biofilm formation, and twitching motility. Bacteriophages often use these filaments as receptors to infect host cells. Here, we describe the identification of a protein that inhibits T4P assembly in Pseudomonas aeruginosa, discovered during a screen for host factors influencing phage infection. We show that expression of PA2560 (renamed PlzR) in P. aeruginosa inhibits adsorption of T4P-dependent phages. PlzR does this by directly binding the T4P chaperone PilZ, which in turn regulates the ATPase PilB and results in disturbed T4P assembly. As the plzR promoter is induced by cyclic di-GMP, PlzR might play a role in coupling T4P function to levels of this second messenger.

Indexed as

Bacterial ProteinsFimbriae, BacterialFimbriae ProteinsPseudomonas aeruginosaCyclic GMPGene Expression Regulation, BacterialMolecular ChaperonesOxidoreductasesPromoter Regions, GeneticProtein BindingBacterial Proteinsbis(3',5')-cyclic diguanylic acidCyclic GMPFimbriae ProteinsMolecular ChaperonesOxidoreductasespilB protein, Bacteria

Identifiers

PMID39379373
PMCPMC11461919

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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.