Effect of Phenylalanine-arginine-beta-naphthylamide to Ciprofloxacin Minimum Inhibitory Concentration Values and Expression of Efflux Pump System Genes in Acinetobacter baumannii Isolates

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dc.authoridKAYİŞ, UĞUR/0000-0003-0020-0857;
dc.authorwosidKAYİŞ, UĞUR/AAV-1646-2021
dc.authorwosidÖkten, Suzan/HJH-6316-2023
dc.authorwosidONURDAG, Fatma KAYNAK/T-2518-2017
dc.authorwosidOkten, Suzan/HGV-1334-2022
dc.contributor.authorOnurdag, Fatma Kaynak
dc.contributor.authorKayis, Ugur
dc.contributor.authorOkten, Suzan
dc.date.accessioned2024-06-12T10:50:28Z
dc.date.available2024-06-12T10:50:28Z
dc.date.issued2021
dc.departmentTrakya Üniversitesien_US
dc.description.abstractThe most realistic approach in recent years is researching the resistance inhibition rather than synthesizing new compounds. In this study, we aimed to determine i) the effect of phenylalanine-argininebeta-naphthylamide (PA beta N), on minimum inhibition concentrations (MICs) of ciprofloxacin (CIP), ii) to obtain the CIP+PA beta N concentration that inhibits CIP resistance and iii) to show that this inhibition is caused by the effect of PA beta N on the expression of efflux pump ( EF) system genes. Acinetobacter baumannii isolates were collected from Trakya University Hospital. In 67 isolates determined to be resistant to CIP, CIP susceptibility was investigated in presence of PA beta N once again. Isolates determined to have four or more fold decrease in ciprofloxacin MIC values were included in checkerboard assay and quantitative real-time reverse transcriptase polymerase chain reaction (qrRT-PCR). Fractional inhibition concentrations (FICs) were calculated through the PA beta N concentrations that inhibit ciprofloxacin resistance, by the checkerboard assay results. With the combination of CIP+PA beta N, the effect of the concentrations at which inhibition occurs, to the expression levels of EF system genes (adeA, adeB, adeR, adeS, adeF, adeG, adeH, adeL) was investigated by qrRT-PCR. By the checker board assay, a synergistic effect was determined between PA beta N and CIP in 11 isolates, while in other isolates the effect was determined to be additive. In some isolates resistant to CIP, CIP + PA beta N combination inhibited the resistance and increased CIP susceptibility. In the presence of 25 mg/L and 100 mg/L PA beta N, 22 (32.83%) and 27 (40.3%) of 67 isolates became sensitive to CIP, respectively. In seven isolates, 12.5 mu g/ml PA beta N concentration eliminated CIP resistance by decreasing CIP MIC value to 1 mu g/ml. Also, in one isolate the MIC value was 0.5 mu g/ml in the presence of 25 mu g/ml PA beta N and 1 mu g/ml in the presence of 1.5625 mu g/ml PA beta N. After analyzing the expression levels of EF genes (adeA, adeB, adeC, adeF, adeG, adeH, adeL, adeR and adeS) by the qRt-PCR method, it was determined that with the addition of PA beta N to media containing CIP, the expression levels of the genes decreased (p< 0.05). The aim of the study has been achieved with the results obtained. These results highlighted the importance of research on the inhibition of resistance, as well as the synthesis of new antimicrobial compounds. Combined use of inhibitors and antibiotics should be considered as an alternative treatment method. Thus, existing antibiotics can be included in the treatment again, saving time and money. It will be possible to use these findings in further studies to elucidate the mechanism of action of new inhibitor candidate compounds and associate them with the expression of DAP genes, also by investigating mutations in the regulatory gene regions in isolates with over-expression levels.en_US
dc.identifier.doi10.5578/mb.20219801
dc.identifier.endpage299en_US
dc.identifier.issn0374-9096
dc.identifier.issue3en_US
dc.identifier.pmid34416797en_US
dc.identifier.scopus2-s2.0-85114094791en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage285en_US
dc.identifier.trdizinid445431en_US
dc.identifier.urihttps://doi.org/10.5578/mb.20219801
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/445431
dc.identifier.urihttps://hdl.handle.net/20.500.14551/17990
dc.identifier.volume55en_US
dc.identifier.wosWOS:000674351200001en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isotren_US
dc.publisherAnkara Microbiology Socen_US
dc.relation.ispartofMikrobiyoloji Bultenien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcinetobacter Baumanniien_US
dc.subjectPhenylalanine-Arginine-Beta-Naphthylamideen_US
dc.subjectCiprofloxacinen_US
dc.subjectResistanceen_US
dc.subjectEfflux Pumpen_US
dc.subjectGene Expressionen_US
dc.subjectPseudomonas-Aeruginosaen_US
dc.subjectMultidrug-Resistanceen_US
dc.subjectEscherichia-Colien_US
dc.subjectAdeabcen_US
dc.subject1-(1-Naphthylmethyl)-Piperazineen_US
dc.subjectCombinationen_US
dc.subjectAciden_US
dc.titleEffect of Phenylalanine-arginine-beta-naphthylamide to Ciprofloxacin Minimum Inhibitory Concentration Values and Expression of Efflux Pump System Genes in Acinetobacter baumannii Isolatesen_US
dc.typeArticleen_US

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