Evidence map›Paper›PMID 41406044›Full record

ArticleChemistry & biodiversity2026

Action of Betulinic Acid in the Inhibition of Efflux Pump NorA in Staphylococcus aureus Strains: In Vitro and In Silico Approaches.

Camila Aparecida Pereira da Silva, Nara Juliana Santos Araujo, Cícera Datiane Morais Oliveira-Tintino, José Maria Barbosa Filho, Gabriel Gonçalves Alencar, José Bezerra de Araújo-Neto, Josefa Sayonara Dos Santos, Juliete Bezerra Soares, Carolina Bandeira Domiciano, Henrique Douglas Melo Coutinho and 1 more

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 2026. 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

11 authors.

Camila Aparecida Pereira da SilvaGraduate Program in Health Sciences, Federal University of Cariri, Barbalha, Brazil.
Nara Juliana Santos AraujoLaboratory of Applied Microbiology-LAMAP, Federal University of Cariri, Barbalha, Brazil.
Cícera Datiane Morais Oliveira-TintinoLaboratory of Microbiology and Molecular Biology, Regional University of Cariri - LMBM, Crato, Brazil.
José Maria Barbosa FilhoFederal University of Paraiba - UFPB, João Pessoa, Brazil.
Gabriel Gonçalves AlencarLaboratory of Microbiology and Molecular Biology, Regional University of Cariri - LMBM, Crato, Brazil.
José Bezerra de Araújo-NetoGraduate Program in Biological Sciences, Biosciences Center, Federal University of Pernambuco, Recife, Brazil.
Josefa Sayonara Dos SantosMulticenter Postgraduate Program in Biochemistry and Molecular Biology, Federal University of Cariri, Barbalha, Brazil.
Juliete Bezerra SoaresMulticenter Postgraduate Program in Biochemistry and Molecular Biology, Federal University of Cariri, Barbalha, Brazil.
Carolina Bandeira DomicianoFederal University of Paraiba - UFPB, João Pessoa, Brazil.
Henrique Douglas Melo CoutinhoLaboratory of Microbiology and Molecular Biology, Regional University of Cariri - LMBM, Crato, Brazil.ORCID https://orcid.org/0000-0002-6634-4207
Jacqueline Cosmo Andrade-PinheiroGraduate Program in Health Sciences, Federal University of Cariri, Barbalha, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibiotic resistance poses a serious challenge to public health, particularly in the case of Staphylococcus aureus, a Gram-positive bacterium that employs multiple resistance mechanisms, including efflux pumps such as NorA, which extrude antimicrobial compounds from the cell and reduce antibiotic efficacy. Therefore, the search for substances capable of inhibiting these mechanisms represents a promising strategy to combat bacterial resistance. Betulinic acid (BA), a pentacyclic triterpene of the lupane type, commonly found in different parts of plants, has demonstrated various pharmacological activities, including antibacterial effects. This study investigated, through in vitro and in silico analyses, the inhibitory action of BA on the NorA efflux pump in S. aureus strains SA-1199 and SA-1199B. The minimum inhibitory concentrations (MICs) were determined using the broth microdilution method. Subsequently, their effects on efflux pump-mediated antibiotic resistance were evaluated by reducing the MIC of the antibiotic and ethidium bromide (EtBr), while fluorimetry and permeability potential tests were carried out using the SYTOX Green fluorescence method. Although BA did not show intrinsic antibacterial activity, showing MIC ≥ 1024 µg/mL, it was able to decrease the MIC of norfloxacin and EtBr, as well as influence membrane permeability and increase fluorescence emission. The results, therefore, indicate that BA has considerable potential as an efflux pump inhibitor and could help in the treatment of resistant bacterial infections.

Indexed as

Anti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsBacterial ProteinsPentacyclic TriterpenesStaphylococcus aureusTriterpenesBetulinic AcidDose-Response Relationship, DrugMicrobial Sensitivity TestsMolecular Docking SimulationMolecular StructureStructure-Activity RelationshipAnti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsBacterial ProteinsBetulinic AcidNorA protein, StaphylococcusPentacyclic TriterpenesTriterpenesbetulinic acidefflux pumppentacyclic triterpeneresistanceStaphylococcus aureus

Identifiers

PMID41406044
PMCPMC12860514

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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.