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Molecular diversity of Klebsiella pneumoniae clinical isolates: antimicrobial resistance, virulence, and biofilm formation

Title: Molecular diversity of Klebsiella pneumoniae clinical isolates: antimicrobial resistance, virulence, and biofilm formation
Authors: Kafa, Ayşe Hümeyra Taşkın; Aslan, Rukiye; Daştan, Sevgi Durna; Çelik, Cem; Hasbek, Mürşit; Eminoğlu, Ayşenur
Publisher Information: Taylor & Francis Ltd.
Publication Year: 2024
Subject Terms: Klebsiella pneumoniae; Antibiotic resistance; Carbapenemase; Biofilm
Description: One 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.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: Nucleosides, Nucleotides & Nucleic Acids; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Taşkın 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/10.1080/15257770.2024.2344741; https://doi.org/10.1080/15257770.2024.2344741; https://hdl.handle.net/11436/9057
DOI: 10.1080/15257770.2024.2344741
Availability: https://hdl.handle.net/11436/9057; https://doi.org/10.1080/15257770.2024.2344741
Rights: info:eu-repo/semantics/closedAccess
Accession Number: edsbas.74246DA8
Database: BASE