Evidence map›Paper›PMID 36008485›Full record

ArticleCommunications biology2022

The membrane-active polyaminoisoprenyl compound NV716 re-sensitizes Pseudomonas aeruginosa to antibiotics and reduces bacterial virulence.

Gang Wang, Jean-Michel Brunel, Matthias Preusse, Negar Mozaheb, Sven D Willger, Gerald Larrouy-Maumus, Pieter Baatsen, Susanne Häussler, Jean-Michel Bolla, Françoise Van Bambeke

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  11. mSphere · 2024
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  16. bioRxiv : the preprint server for biology · 2023
    Article
  17. Article
  18. Poly-L-Lysine to Fight Antibiotic Resistances ofInternational journal of molecular sciences · 2023
    Article
  19. 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

10 authors at 6 institutions in 5 countries.

Gang WangPharmacologie cellulaire et moléculaire, Louvain Drug Research Institute, Université catholique de Louvain, Brussels, Belgium.
Jean-Michel BrunelAix Marseille Université, INSERM, SSA, Membranes et Cibles thérapeutiques (MCT), Marseille, France.ORCID 0000-0002-9355-8980
Matthias PreusseDepartment of Molecular Bacteriology, Helmoltz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0002-2775-3139
Negar MozahebPharmacologie cellulaire et moléculaire, Louvain Drug Research Institute, Université catholique de Louvain, Brussels, Belgium.ORCID 0000-0001-6259-9512
Sven D WillgerDepartment of Molecular Bacteriology, Helmoltz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0002-9736-2926
Gerald Larrouy-MaumusDepartment of Life Sciences, Faculty of Natural Sciences, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, United Kingdom.
Pieter BaatsenElectron Microscopy Platform & Bio Imaging Core, VIB & KULeuven Center for Brain & Disease Research, KULeuven, Leuven, Belgium.
Susanne HäusslerDepartment of Molecular Bacteriology, Helmoltz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0001-6141-9102
Jean-Michel BollaAix Marseille Université, INSERM, SSA, Membranes et Cibles thérapeutiques (MCT), Marseille, France.ORCID 0000-0003-3892-4340
Françoise Van BambekePharmacologie cellulaire et moléculaire, Louvain Drug Research Institute, Université catholique de Louvain, Brussels, Belgium. francoise.vanbambeke@uclouvain.be.ORCID 0000-0002-0052-7991
UCLouvain · BEHelmholtz Centre for Infection Research · DEInserm · FRImperial College London · GBRigshospitalet · DKVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudomonas aeruginosa is intrinsically resistant to many antibiotics due to the impermeability of its outer membrane and to the constitutive expression of efflux pumps. Here, we show that the polyaminoisoprenyl compound NV716 at sub-MIC concentrations re-sensitizes P. aeruginosa to abandoned antibiotics by binding to the lipopolysaccharides (LPS) of the outer membrane, permeabilizing this membrane and increasing antibiotic accumulation inside the bacteria. It also prevents selection of resistance to antibiotics and increases their activity against biofilms. No stable resistance could be selected to NV716-itself after serial passages with subinhibitory concentrations, but the transcriptome of the resulting daughter cells shows an upregulation of genes involved in the synthesis of lipid A and LPS, and a downregulation of quorum sensing-related genes. Accordingly, NV716 also reduces motility, virulence factors production, and biofilm formation. NV716 shows a unique and highly promising profile of activity when used alone or in combination with antibiotics against P. aeruginosa, combining in a single molecule anti-virulence and potentiator effects. Additional work is required to more thoroughly understand the various functions of NV716.

Indexed as

Anti-Bacterial AgentsPseudomonas aeruginosaBiofilmsLipopolysaccharidesQuorum SensingAnti-Bacterial AgentsLipopolysaccharides

Identifiers

PMID36008485
PMCPMC9411590
OpenAlexW4293086762

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.