Evidence map›Paper›PMID 39565046›Full record

ArticleChemMedChem2025

Selenocompounds as Potent Efflux Pump Inhibitors on Gram-positive Bacteria.

Annamária Kincses, Nikoletta Szemerédi, Miguel Benito-Lama, Dávid Dózsai, Ákos Csonka, Enrique Domínguez-Álvarez, Gabriella Spengler

Abstract read
In one paragraph

Article in ChemMedChem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Annamária KincsesDepartment of Medical Microbiology, Albert Szent-Györgyi Health Center and Albert Szent-Györgyi Medical School, University of Szeged, Semmelweis street 6, 6725, Szeged, Hungary.ORCID https://orcid.org/0000-0002-1591-1419
Nikoletta SzemerédiDepartment of Medical Microbiology, Albert Szent-Györgyi Health Center and Albert Szent-Györgyi Medical School, University of Szeged, Semmelweis street 6, 6725, Szeged, Hungary.
Miguel Benito-LamaInstituto de Química Orgánica General (IQOG), Consejo Superior de Organizaciones Científicas (CSIC), Juan de la Cierva 3, 28006, Madrid, Spain.
Dávid DózsaiDepartment of Traumatology, Albert Szent-Györgyi Health Center and Albert Szent-Györgyi Medical School, University of Szeged, Semmelweis street 6, 6725, Szeged, Hungary.
Ákos CsonkaDepartment of Traumatology, Albert Szent-Györgyi Health Center and Albert Szent-Györgyi Medical School, University of Szeged, Semmelweis street 6, 6725, Szeged, Hungary.
Enrique Domínguez-ÁlvarezInstituto de Química Orgánica General (IQOG), Consejo Superior de Organizaciones Científicas (CSIC), Juan de la Cierva 3, 28006, Madrid, Spain.
Gabriella SpenglerDepartment of Medical Microbiology, Albert Szent-Györgyi Health Center and Albert Szent-Györgyi Medical School, University of Szeged, Semmelweis street 6, 6725, Szeged, Hungary.ORCID https://orcid.org/0000-0001-8085-0950

Funding

Agencia Estatal Consejo Superior de Investigaciones CientíficasAgencia Estatal de Investigación MCIN/AEI/10.13039/501100011033Development and Innovation Fund"ERDF A way of making Europe" PID2022-136438OB-I00Hungarian Academy of Sciences BO/00158/22/5Hungarian Academy of Sciences ÚNKP-21-3-SZTE-103Hungarian Academy of Sciences ÚNKP-23-4-SZTE-215iLINK project LINKA20285New National Excellence Program of the Ministry for Culture and Innovation from the source of the National ResearchSzeged Foundation for Cancer Research
6 · The paper itself

Abstract

In recent years, selenocompounds have gained increasing attention as potential anticancer and antibacterial agents. Several selenoderivatives have been confirmed to act as MDR efflux pump inhibitors, based on their in vitro results against the bacterial AcrAB-TolC system and the cancer MDR efflux pump P-glycoprotein. Efflux pumps can contribute directly or indirectly to the virulence of bacteria, as they can reduce the intracellular concentration of antibacterial substances by expelling them out of the cell. The present work aims to study the antibacterial and efflux pump inhibiting properties of four families of selenoesters, namely aspirin-selenoesters, phenone-selenoesters, hydroxy-selenoesters, and benzyl-selenoesters. The real-time ethidium bromide accumulation assay confirmed that these derivatives inhibited the efflux systems of methicillin-resistant Staphylococcus aureus (MRSA) without exerting any antibacterial effect. The relative expression of efflux pump gene of NorA transporter was also monitored in the presence of the most potent derivatives on reference S. aureus, finding that these derivatives could change the expression of the tested efflux pump gene. Regarding the anti-biofilm activity, aspirin-selenoesters, benzyl-selenoesters, and hydroxy-selenoesters could efficiently inhibit the biofilm production of the MRSA strain. It can be concluded that selenocompounds could act as efflux pump inhibitors, thus reducing the virulence of biofilm-producing bacteria.

Indexed as

Anti-Bacterial AgentsMethicillin-Resistant Staphylococcus aureusOrganoselenium CompoundsATP-Binding Cassette, Sub-Family C ProteinsBacterial ProteinsBiofilmsDose-Response Relationship, DrugMicrobial Sensitivity TestsMolecular StructureStructure-Activity RelationshipAnti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsBacterial ProteinsOrganoselenium CompoundsBiofilmBiological activityEfflux pumpMultidrug resistanceSelenium

Identifiers

PMID39565046
PMCPMC11733404

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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.