TY - JOUR
T1 - CTX-M-15 carried on Incn-type plasmids in Klebsiella pneumoniae
AU - Aktaş, Zerrin
AU - Gönüllü, Nevriye
AU - Kayacan, Zeynep Çiǧdem
AU - Anǧ, Özdem
AU - Carattoli, Alessandra
AU - Yong, Dong Eun
AU - Walsh, Timothy R.
PY - 2009
Y1 - 2009
N2 - Objective: The aim of this study was to characterize the CTX-M genes in clinical isolates of Klebsiella pneumoniae, particularly, the plasmid types that carry them. Material and Methods: Antimicrobial susceptibilities were determined by the agar dilution and E-test. Beta-lactamase production as analyzed by phenotypic tests [E-test MBL and extended spectrum β-lactamase (ESBL), isoelectric focusing, and bioassay] and molecular methods [polymerase chain reaction (PCR) detection of ESBL-encoding genes and IS elements, DNA sequencing and analysis of blaCTX-M and ISEcP1 PCR amplicons, typing by randomly amplified polymorphic DNA (RAPD) analysis and plasmid isolation, transformation, rep-typing and IncN plasmid confirmation]. Results: Thirty four (14.8%) out of 230 clinical isolates of K. pneumoniae were found as ESBL producers. The isolates produced one to five different β-lactamases, according to the isoelectric focusing results. The prevalence of the CTX-M-type ESBLs was found as 35% and sequencing proved all as CTX-M-15. RAPD analysis showed no clonal relation between the strains. Previous studies have shown that the blaCTX-M-15 gene was carried on FII plasmids. In 10 strains in this study, the CTX-M-15 gene was on 95 kb-larger plasmids typing to IncN. In two isolates the blaCTX-M-15 was carried on an approximately 60 kb plasmid and possessed an Inc/rep type of FII. Conclusion: This is the first report of IncN carrying blaCTX-M-15 and confirms the rapid emergence of CTX-M-15 enzymes among K. pneumoniae in Istanbul. Through this study, it was aimed to underline the risk of spread of IncN type plasmids, among gram-negative bacteria in Turkey, as shown previously in Greece.
AB - Objective: The aim of this study was to characterize the CTX-M genes in clinical isolates of Klebsiella pneumoniae, particularly, the plasmid types that carry them. Material and Methods: Antimicrobial susceptibilities were determined by the agar dilution and E-test. Beta-lactamase production as analyzed by phenotypic tests [E-test MBL and extended spectrum β-lactamase (ESBL), isoelectric focusing, and bioassay] and molecular methods [polymerase chain reaction (PCR) detection of ESBL-encoding genes and IS elements, DNA sequencing and analysis of blaCTX-M and ISEcP1 PCR amplicons, typing by randomly amplified polymorphic DNA (RAPD) analysis and plasmid isolation, transformation, rep-typing and IncN plasmid confirmation]. Results: Thirty four (14.8%) out of 230 clinical isolates of K. pneumoniae were found as ESBL producers. The isolates produced one to five different β-lactamases, according to the isoelectric focusing results. The prevalence of the CTX-M-type ESBLs was found as 35% and sequencing proved all as CTX-M-15. RAPD analysis showed no clonal relation between the strains. Previous studies have shown that the blaCTX-M-15 gene was carried on FII plasmids. In 10 strains in this study, the CTX-M-15 gene was on 95 kb-larger plasmids typing to IncN. In two isolates the blaCTX-M-15 was carried on an approximately 60 kb plasmid and possessed an Inc/rep type of FII. Conclusion: This is the first report of IncN carrying blaCTX-M-15 and confirms the rapid emergence of CTX-M-15 enzymes among K. pneumoniae in Istanbul. Through this study, it was aimed to underline the risk of spread of IncN type plasmids, among gram-negative bacteria in Turkey, as shown previously in Greece.
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M3 - Article
AN - SCOPUS:76749151961
SN - 1300-0292
VL - 29
SP - 1355
EP - 1364
JO - Turkiye Klinikleri Journal of Medical Sciences
JF - Turkiye Klinikleri Journal of Medical Sciences
IS - 6
ER -