Evidence map›Paper›PMID 35032112›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Pseudomonas aeruginosa Biofilm Dispersion by the Human Atrial Natriuretic Peptide.

Mélissande Louis, Thomas Clamens, Ali Tahrioui, Florie Desriac, Sophie Rodrigues, Thibaut Rosay, Nicholas Harmer, Suraya Diaz, Magalie Barreau, Pierre-Jean Racine and 8 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

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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

18 authors at 4 institutions in 2 countries.

Mélissande LouisLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.
Thomas ClamensLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0002-0164-5375
Ali TahriouiLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0003-4064-820X
Florie DesriacLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0002-6436-6437
Sophie RodriguesLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0001-8901-3032
Thibaut RosayLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0001-6945-4850
Nicholas HarmerSchool of Biosciences, University of Exeter, Exeter, EX4 4QD, UK.ORCID 0000-0002-4073-0505
Suraya DiazSchool of Biosciences, University of Exeter, Exeter, EX4 4QD, UK.
Magalie BarreauLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0002-9509-6054
Pierre-Jean RacineLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0003-1747-6737
Eric KipnisUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, Lille, France, University Lille, Lille, F-59000, France.ORCID 0000-0001-8887-7330
Teddy GrandjeanUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR9017-CIIL-Centre d'Infection et d'Immunité de Lille, Lille, France, University Lille, Lille, F-59000, France.ORCID 0000-0002-6244-0154
Julien VieillardNormandie Univ, UNIROUEN, INSA Rouen, CNRS, COBRA (UMR 6014), Evreux, 27000, France.
Emeline BouffartiguesLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0003-2569-4961
Pierre CornelisLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0002-3179-4654
Sylvie ChevalierLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0001-6489-438X
Marc G J FeuilloleyLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0001-6467-4336
Olivier LesouhaitierLaboratory of Microbiology Signals and Microenvironment LMSM EA 4312, University of Rouen Normandy, Evreux, 27000, France.ORCID 0000-0001-8235-8919
Université de Rouen Normandie · FRCentre National de la Recherche Scientifique · FRUniversity of Exeter · GBNormandie Université · FR

Funding

Region Normandy, the InterReg IVA PeReNE project and from the Normandy Valorisation cluster
6 · The paper itself

Abstract

Pseudomonas aeruginosa biofilms cause chronic, antibiotic tolerant infections in wounds and lungs. Numerous recent studies demonstrate that bacteria can detect human communication compounds through specific sensor/receptor tools that modulate bacterial physiology. Consequently, interfering with these mechanisms offers an exciting opportunity to directly affect the infection process. It is shown that the human hormone Atrial Natriuretic Peptide (hANP) both prevents the formation of P. aeruginosa biofilms and strongly disperses established P. aeruginosa biofilms. This hANP action is dose-dependent with a strong effect at low nanomolar concentrations and takes effect in 30-120 min. Furthermore, although hANP has no antimicrobial effect, it acts as an antibiotic adjuvant. hANP enhances the antibiofilm action of antibiotics with diverse modes of action, allowing almost full biofilm eradication. The hANP effect requires the presence of the P. aeruginosa sensor AmiC and the AmiR antiterminator regulator, indicating a specific mode of action. These data establish the activation of the ami pathway as a potential mechanism for P. aeruginosa biofilm dispersion. hANP appears to be devoid of toxicity, does not enhance bacterial pathogenicity, and acts synergistically with antibiotics. These data show that hANP is a promising powerful antibiofilm weapon against established P. aeruginosa biofilms in chronic infections.

Indexed as

Atrial Natriuretic FactorPseudomonas aeruginosaAnti-Bacterial AgentsBiofilmsHumansVirulenceAnti-Bacterial AgentsAtrial Natriuretic Factorami pathwayantibioticsbacterial adaptationbacterial sensorbiofilm dispersionhANPnatriuretic peptidesPseudomonas aeruginosa

Identifiers

PMID35032112
PMCPMC8895129
OpenAlexW4206702820

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.