Evidence map›Paper›PMID 41733756›Full record

ArticleMolecular biology reports2026

The synergistic antibacterial and anti-biofilm effects of fluoxetine and quercetin against carbapenemase producing Stenotrophomonas maltophilia clinical isolates.

Dhay A Azeez, Fouad Qasim Jubair Al-Zayadi, Ali S Shakir

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Dhay A AzeezDepartment of Biology, College of Science, Al-Muthanna University, Samawah, Iraq.
Fouad Qasim Jubair Al-ZayadiDepartment of Biology, College of Education for Pure Sciences, Al-Muthanna University, Samawah, Iraq. fouad.qasim@mu.edu.iq.ORCID http://orcid.org/0000-0002-2662-0203
Ali S ShakirCollege of Dentistry, University of Al-Qadisiyah, Diwaniyah, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStenotrophomonas maltophilia (S. maltophilia) drug resistance is a crisis worldwide. Our objective was evaluation of synergistic antibacterial and anti-biofilm effects of fluoxetine and quercetin against carbapenemase producing S. maltophilia (CR-St) clinical isolates.

methodsThirty CR-St isolates were recovered from various clinical specimens. Various concentrations of imipenem, quercetin and fluoxetine were prepared for the antibacterial tests. The expression of SmeE efflux pump gene was evaluated in exposure to quercetin and fluoxetine using quantitative real-time PCR. Anti-biofilm effects and time kill assay tests were also performed.

resultsThe isolates exhibited high level resistance to imipenem (MIC: 8–64 µg/mL) but inferred resistance to fluoxetine (MIC: 128–256 µg/mL) and quercetin (MIC: 128–512 µg/mL) at higher concentrations. The fluoxetine and quercetin (1:1 ratio) had strong antibacterial activity since the synergistic effects of the two compounds significantly reduced the MIC values and also provided bactericidal activity data in time-kill studies. All isolates produced biofilms, and most produced moderate to strong biofilms. Fluoxetine and quercetin inhibited biofilm formation and disrupted pre-formed biofilms to lesser degree. The fluoxetine and quercetin combination had synergistic capabilities by decreasing biofilm formation up to 85% and disruption of mature biofilms with some observed structural destruction. The expression of SmeE efflux pump gene was decreased in exposure to quercetin by 2.2 fold (p < 0.0001).

conclusionQuercetin and fluoxetine could potentially exert anti-biofilm and antibacterial effects against CR-St with synergistic properties in vitro.

Indexed as

Anti-Bacterial AgentsBacterial Proteinsbeta-LactamasesBiofilmsFluoxetineQuercetinStenotrophomonas maltophiliaDrug Resistance, BacterialDrug SynergismHumansImipenemMicrobial Sensitivity TestsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseFluoxetineImipenemQuercetinBiofilmsDrug resistanceFluoxetineQuercetinStenotrophomonas maltophilia

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PMID41733756

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