Evidence map›Paper›PMID 42086869›Full record

ArticleScientific reports2026

ASO-functionalized gold nanoparticles for gene silencing in drug-resistant Pseudomonas aeruginosa: a proof-of-concept study.

Sarah Najah AlJanabi, Maroua Gdoura-Ben Amor, Wathiq Abbas Al-Draghi, Hanen Sellami, Olfa Frikha-Gargouri

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Article in Scientific 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sarah Najah AlJanabiDepartment of Biology, Faculty of Science, University of Sfax, Sfax, Tunisia. rayanabb15@gmail.com.
Maroua Gdoura-Ben AmorResearch Laboratory of Environmental Toxicology Microbiology and Health (LR17ES06), Faculty of Sciences, Sfax University, BP 1171, Sfax, 3000, Tunisia.
Wathiq Abbas Al-DraghiThe Institute of Genetic Engineering and Biotechnology for Postgraduate Studies, Baghdad University, Baghdad, Iraq.
Hanen SellamiLaboratory of Treatment and Valorization of Water Rejects, Water Research and Technologies Center (CERTE), Borj-Cedria Technopark, University of Carthage, Soliman, 8020, Tunisia.
Olfa Frikha-GargouriLaboratory of Biopesticides, Centre of Biotechnology of Sfax, Sfax University, P.O. Box 1177, Sfax, 3018, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present work aims at evaluating a novel therapeutic technique against clinical samples of Pseudomonas aeruginosa, a multiple drug resistant bacterium by integrating gold nanoparticles (AuNPs) with antisense oligonucleotide (ASO) (ASO-AuNPs) to target and silence the blaVIM and blaCTX-M genes. The objectives were to evaluate the ability of ASO-AuNPs to silence resistance genes and reduce their expression to combat antibiotic resistance. Seventy P. aeruginosa clinical isolates collected from Iraqi hospitals were isolated, identified and their antibiotic resistance profiles were assessed. The blaVIM and blaCTX-M genes were detected by PCR. These genes were engineered through the use of ASO-AuNPs. Resistance to carbapenem and cephalosporin and quantitative blaVIM and blaCTX-M gene expression in P. aeruginosa were further studied before and after silencing. The blaVIM gene was found in 79.2% of carbapenem-resistant samples, while blaCTX-M was identified in 72.7% of cephalosporin-resistant samples. A significant reduction in antibiotic resistance was achieved following ASO-AuNPs application. Moreover, the gene silencing technique significantly decreased the expression of blaVIM and blaCTX-M genes. The mean fold change of the CTX-M gene was 15.92 before and 1.36 after gene silencing, that of the blaVIM gene was 0.63 and 0.51, respectively. These findings provide a proof-of-concept for the use of ASO-functionalized gold nanoparticles as a potential strategy for targeting antibiotic resistance genes in P. aeruginosa, with potential applications in managing resistant infections in healthcare settings.

Indexed as

Drug Resistance, Multiple, BacterialGene SilencingGoldMetal NanoparticlesOligonucleotides, AntisensePseudomonas aeruginosaAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesHumansMicrobial Sensitivity TestsProof of Concept StudyPseudomonas InfectionsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesGoldOligonucleotides, AntisenseblaCTX-MblaVIMGene silencingGold nanoparticlesMulti-drug resistant

Identifiers

PMID42086869
PMCPMC13333920

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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.