Detection Of Carbapenem-Resistant Klebsiella Pneumoniae Strains Harboring Carbapenemase, Beta-Lactamase And Quinolone Resistance Genes İn İntensive Care Unit Patients
dc.authorid | 243533 | en_US |
dc.authorid | 107955 | en_US |
dc.contributor.author | Demirci, Mehmet | |
dc.contributor.author | Ünlü, Özge | |
dc.date.accessioned | 2021-01-27T10:21:01Z | |
dc.date.available | 2021-01-27T10:21:01Z | |
dc.date.issued | 2020 | |
dc.department | İstanbul Beykent Üniversitesi | en_US |
dc.description.abstract | Aim: Carbapenem-resistant Klebsiella pneumoniae (CR-Kp) strains are important nosocomial pathogens worldwide. In this study, we aimed to reveal the antibiotic resistance of clinical CR-Kp strains and determine the presence of KPC, OXA-48, VIM and IMP carbapenemase genes. CTX-M-1, TEM-1, SHV-1 extended-spectrum beta-lactamase (ESBL) genes, qnrA, qnrB, qnrS plasmid-mediated quinolone resistance genes and sul1 and sul2 sulfonamide resistance genes provided molecular epidemiological data. Methods: A total of 175 K. pneumoniae strains were isolated from clinical samples of patients hospitalised in an intensive care unit (ICU) betweent April and October 2017. The strains were identified with conventional methods, with VITEK 2 (BioMerieux, France) and MALDI-TOF MS (Bruker, USA). Antimicrobial susceptibilities were tested using the disc-diffusion method and E-test (BioMerieux, France). Antimicrobial resistance genes were investigated via real-time PCR in strains identified as CR-Kp. Results: High frequencies of blaTEM-1 (86.36%), blaSHV-1 (86.36%), and blaCTX-M-1 (95.45%) genes were found in CR-Kp strains. Morever, all three ESBL genes coexisted in 77.3% of all strains. blaKPC was detected in 12 (54.55%) of the strains, and 4 of them which had an MIC> 16 ?g/mL to imipenem showed blaOXA-48 positivity as well. The qnrS gene determinant (86.36%) had the highest frequency, and strains carrying qnrA showed higher MICs for ciprofloxacin. Conclusion: CR-Kp strains are able to develop different antimicrobial resistance patterns according to regional changes in antimicrobial therapeutic policies. Thus, it is important to monitor the regional molecular epidemiological data for efficient treatment. | en_US |
dc.identifier.citation | GMS Hygiene and Infection Control 2020, Vol. 15 | en_US |
dc.identifier.doi | 10.3205/dgkh000366 | |
dc.identifier.issn | 1029-8479 | |
dc.identifier.pmid | 33299744 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.3205/dgkh000366 | |
dc.identifier.wos | WOS:000598118300001 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Deutsche Gesellschaft für Krankenhaushygiene | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.subject | Carbapenem-resistant Klebsiella pneumoniae | en_US |
dc.subject | Beta lactamase | en_US |
dc.subject | Carbapenemase | en_US |
dc.subject | Quinolone resistance | en_US |
dc.title | Detection Of Carbapenem-Resistant Klebsiella Pneumoniae Strains Harboring Carbapenemase, Beta-Lactamase And Quinolone Resistance Genes İn İntensive Care Unit Patients | en_US |
dc.title.alternative | Nachweis von Carbapenem-resistenten Klebsiella pneumoniae-Stämmen mit Carbapenemase-, Beta-Lactamase- und Chinolon-Resistenzgenen bei Patienten einer Intensivpflegestation | en_US |
dc.type | Article | en_US |
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