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Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae

INTRODUCTION: Klebsiella pneumoniae (K. pneumoniae) is an important opportunistic pathogen causes serious community and hospital-acquired infections, which is highly resistant to antibiotics. We aimed to determine the frequency of multidrug resistant (MDR) and molecular typing of clinical isolates o...

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Autores principales: Akya, Alisha, Elahi, Azam, Chegenelorestani, Roya, Rezaee, Mahya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932916/
https://www.ncbi.nlm.nih.gov/pubmed/29744322
http://dx.doi.org/10.4103/ijabmr.IJABMR_333_16
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author Akya, Alisha
Elahi, Azam
Chegenelorestani, Roya
Rezaee, Mahya
author_facet Akya, Alisha
Elahi, Azam
Chegenelorestani, Roya
Rezaee, Mahya
author_sort Akya, Alisha
collection PubMed
description INTRODUCTION: Klebsiella pneumoniae (K. pneumoniae) is an important opportunistic pathogen causes serious community and hospital-acquired infections, which is highly resistant to antibiotics. We aimed to determine the frequency of multidrug resistant (MDR) and molecular typing of clinical isolates of K. pneumoniae. METHODOLOGY: One hundred isolates of K. pneumoniae were collected from clinical samples in three general hospitals in Kermanshah. The antimicrobial susceptibility and extended-spectrum beta-lactamases (ESBL) production of isolates were determined using disk diffusion and combined disk methods, respectively. The bla(CTX-M) gene, class I and II integrons were detected using polymerase chain reaction. The bla(CTX-M) positive isolates were selected for genotyping using pulsed-field gel electrophoresis (PFGE). RESULTS: MDR phenotype was observed in 56% of isolates. The 40% of isolates were ESBL positive and 35 isolates contained bla(CTX-M). Class I and II of integrons were detected in 50 (89.2%) and 39 (69.6%) of MDR isolates, respectively. PFGE patterns of K. pneumoniae bla(CTX-M) positive isolates indicated 19 clusters (X(1-19)) with different genotype patterns. CONCLUSIONS: The study findings highlight the concern of circulating MDR strains of K. pneumoniae with bla(CTX-M) and class I and II integrons in Kermanshah hospitals. The presence of integrons among isolates may facilitate the spread of new resistance genes in this bacterium. Therefore, surveillance for the spread of MDR strains of this bacterium is recommended in hospitals.
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spelling pubmed-59329162018-05-09 Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae Akya, Alisha Elahi, Azam Chegenelorestani, Roya Rezaee, Mahya Int J Appl Basic Med Res Original Article INTRODUCTION: Klebsiella pneumoniae (K. pneumoniae) is an important opportunistic pathogen causes serious community and hospital-acquired infections, which is highly resistant to antibiotics. We aimed to determine the frequency of multidrug resistant (MDR) and molecular typing of clinical isolates of K. pneumoniae. METHODOLOGY: One hundred isolates of K. pneumoniae were collected from clinical samples in three general hospitals in Kermanshah. The antimicrobial susceptibility and extended-spectrum beta-lactamases (ESBL) production of isolates were determined using disk diffusion and combined disk methods, respectively. The bla(CTX-M) gene, class I and II integrons were detected using polymerase chain reaction. The bla(CTX-M) positive isolates were selected for genotyping using pulsed-field gel electrophoresis (PFGE). RESULTS: MDR phenotype was observed in 56% of isolates. The 40% of isolates were ESBL positive and 35 isolates contained bla(CTX-M). Class I and II of integrons were detected in 50 (89.2%) and 39 (69.6%) of MDR isolates, respectively. PFGE patterns of K. pneumoniae bla(CTX-M) positive isolates indicated 19 clusters (X(1-19)) with different genotype patterns. CONCLUSIONS: The study findings highlight the concern of circulating MDR strains of K. pneumoniae with bla(CTX-M) and class I and II integrons in Kermanshah hospitals. The presence of integrons among isolates may facilitate the spread of new resistance genes in this bacterium. Therefore, surveillance for the spread of MDR strains of this bacterium is recommended in hospitals. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5932916/ /pubmed/29744322 http://dx.doi.org/10.4103/ijabmr.IJABMR_333_16 Text en Copyright: © 2018 International Journal of Applied and Basic Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Akya, Alisha
Elahi, Azam
Chegenelorestani, Roya
Rezaee, Mahya
Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae
title Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae
title_full Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae
title_fullStr Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae
title_full_unstemmed Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae
title_short Dissemination of Multidrug-Resistant, Class I and II Integrons and Molecular Typing of CTX-M-producing Klebsiella pneumoniae
title_sort dissemination of multidrug-resistant, class i and ii integrons and molecular typing of ctx-m-producing klebsiella pneumoniae
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932916/
https://www.ncbi.nlm.nih.gov/pubmed/29744322
http://dx.doi.org/10.4103/ijabmr.IJABMR_333_16
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