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dc.contributor.authorKafa, Ayşe Hümeyra Taşkın
dc.contributor.authorAslan, Rukiye
dc.contributor.authorDaştan, Sevgi Durna
dc.contributor.authorÇelik, Cem
dc.contributor.authorHasbek, Mürşit
dc.contributor.authorEminoğlu, Ayşenur
dc.date.accessioned2024-06-10T07:24:25Z
dc.date.available2024-06-10T07:24:25Z
dc.date.issued2024en_US
dc.identifier.citationTaşkın Kafa, A. H., Aslan, R., Durna Daştan, S., Çeli K, C., Hasbek, M., & Emi Noğlu, A. (2024). Molecular diversity of Klebsiella pneumoniae clinical isolates: antimicrobial resistance, virulence, and biofilm formation. Nucleosides, nucleotides & nucleic acids, 1–17. Advance online publication. https://doi.org/10.1080/15257770.2024.2344741en_US
dc.identifier.issn1525-7770
dc.identifier.issn1532-2335
dc.identifier.urihttps://doi.org/10.1080/15257770.2024.2344741
dc.identifier.urihttps://hdl.handle.net/11436/9057
dc.description.abstractOne of the mechanisms responsible for antibiotic resistance in Klebsiella pneumoniae is the enzymes produced by the bacteria; another important mechanism is the ability to form biofilm. In this study, antibiotic resistance, genes associated with virulence, and biofilm-forming properties of K. pneumoniae strains were investigated. A total of 100 K. pneumoniae isolates were obtained from different clinical samples identified by Matrix-Assisted Laser Desorption/Ionization time-of-flight Mass Spectrometry. Antimicrobial susceptibility testing was performed with the Phoenix 100 apparatus. The biofilm forming properties of strains were determined by the microtiter plate method. For molecular analysis, genes encoding the carbapenemase enzyme (bla(OXA-48), bla(NDM-1), bla(IMP), and bla(VIM)) and biofilm-related genes (treC, luxS, mrkA, and wza) were investigated by polymerase chain reaction (PCR). While 76% of clinical isolates were resistant to three or more antimicrobials, 24% were classified as non-multidrug resistant (non-MDR). When biofilm-forming capacities of clinical isolates were tested, it was determined that the resistant-isolates produced 59.2% strong biofilm, and susceptible-isolates produced 12.5% strong biofilm. According to PCR results, carbapenemase genes were determined as follows: bla(OXA-48)-70%, bla(NDM)-49%, and bla(KPC)-19%, bla(OXA-48)/bla(NDM)/bla(KPC)-12%, bla(OXA-48)/bla(NDM)-26%, and bla(OXA-48)/bla(KPC)-4%. The biofilm-associated genes in bacterial isolates were determined as follows: luxS-98%, treC-94%, mrkA-88%, and wza-15%. In addition, Hierarchical Clustering Tree and Heatmap analysis revealed an association between isolates that lacks resistance genes and isolates lacks biofilm-formation related genes that were included in MDR or non-MDR classes. As a result, biofilm should be considered in the treatment of MDR infections, and therapy should be planned accordingly. In addition, pursuing the data and genes of antibiotic resistance is significant for combating resistance.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltd.en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectKlebsiella pneumoniaeen_US
dc.subjectAntibiotic resistanceen_US
dc.subjectCarbapenemaseen_US
dc.subjectBiofilmen_US
dc.titleMolecular diversity of Klebsiella pneumoniae clinical isolates: antimicrobial resistance, virulence, and biofilm formationen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Fen - Edebiyat Fakültesi, Biyoloji Bölümüen_US
dc.contributor.institutionauthorEminoğlu, Ayşenur
dc.identifier.doi10.1080/15257770.2024.2344741en_US
dc.relation.journalNucleosides, Nucleotides & Nucleic Acidsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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