Carbapenem-hydrolysing  -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil

Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ES...

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Veröffentlicht in:Journal of antimicrobial chemotherapy 2009-02, Vol.63 (2), p.265-268
Hauptverfasser: Peirano, G., Seki, L. M., Val Passos, V. L., Pinto, M. C. F. G., Guerra, L. R., Asensi, M. D.
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container_end_page 268
container_issue 2
container_start_page 265
container_title Journal of antimicrobial chemotherapy
container_volume 63
creator Peirano, G.
Seki, L. M.
Val Passos, V. L.
Pinto, M. C. F. G.
Guerra, L. R.
Asensi, M. D.
description Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. [PUBLICATION ABSTRACT]
doi_str_mv 10.1093/jac/dkn484
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M. ; Val Passos, V. L. ; Pinto, M. C. F. G. ; Guerra, L. R. ; Asensi, M. D.</creator><creatorcontrib>Peirano, G. ; Seki, L. M. ; Val Passos, V. L. ; Pinto, M. C. F. G. ; Guerra, L. R. ; Asensi, M. D.</creatorcontrib><description>Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. 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D.</creatorcontrib><title>Carbapenem-hydrolysing  -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil</title><title>Journal of antimicrobial chemotherapy</title><description>Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. 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M.</au><au>Val Passos, V. L.</au><au>Pinto, M. C. F. G.</au><au>Guerra, L. R.</au><au>Asensi, M. D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbapenem-hydrolysing  -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><date>2009-02-01</date><risdate>2009</risdate><volume>63</volume><issue>2</issue><spage>265</spage><epage>268</epage><pages>265-268</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. 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source Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Antibiotics
Antimicrobial agents
Drug resistance
Nosocomial infections
Pneumonia
title Carbapenem-hydrolysing  -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil
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