Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran

Background: Multidrug resistant K. pneumoniae, particularly the extended-spectrum β-lactamase (ESBL) producing strains, are often responsible for the failure of antibiotic treatment in nosocomial infections. Employing molecular methods to distinguish between ESBL and non-ESBL producing isolates...

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Main Authors: Fereshteh Eftekhar, Parvaneh Nouri
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2015-01-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/5373/10651_CE(Ra)_F(Sh)_PF1(AJ_Sh)_PFA(AK)_PF2(PAG).pdf
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author Fereshteh Eftekhar
Parvaneh Nouri
author_facet Fereshteh Eftekhar
Parvaneh Nouri
author_sort Fereshteh Eftekhar
collection DOAJ
description Background: Multidrug resistant K. pneumoniae, particularly the extended-spectrum β-lactamase (ESBL) producing strains, are often responsible for the failure of antibiotic treatment in nosocomial infections. Employing molecular methods to distinguish between ESBL and non-ESBL producing isolates can help quick identification of these multidrug resistant pathogens and thereby initiating appropriate antibiotic therapy. The aim of this study was to employ RAPD-PCR to distinguish the genetic fingerprints of ESBL producing clinical isolates of K. pneumoniae from ESBL negative strains. Materials and Methods: Antibacterial susceptibility of 104 K. pneumoniae clinical isolates was determined to 13 antibacterial agents by disc diffusion. ESBL production was measured by the double disc synergy test followed by phenotypic confirmatory tests. Genetic fingerprinting was carried out by RAPD-PCR. Results: All isolates were susceptible to imipenem. Antibiotic resistance rates were: piperacillin (100%), ceftazidime (62.5%), cefotaxime (57.6%), aztreonam (52.8%), cefepime (51.9%), kanamycin (50.9%), gentamicin (41.3%), ciprofloxacin (37.5%), nitrofurantoin (30.6%), nalidixic acid (22.1%), piperacillin/ tazobactam (21.1%) and amikacin (9.6%). ESBL production was observed in 14 isolates (13.4%). Genetic fingerprinting performed on 43 isolates (14 ESBL positive and 29 ESBL negative) by RAPD-PCR, showed that 46.5% of the isolates belonged to a single profile (genotype 1), of which, the majority (62.1%) were non-ESBL producers. Conclusion: RAPD-PCR results showed heterogeneity among the isolates. There was no association between ESBL production with any specific genetic fingerprint.
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spelling doaj.art-bd9b66dfae914d2da45f7ffd39af8b162022-12-21T22:48:44ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2015-01-0191DC01DC0310.7860/JCDR/2015/10651.5373Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in TehranFereshteh Eftekhar0Parvaneh Nouri1Associate Professor, Department of Microbiology, Faculty of Biological Sciences, Shahid Beheshti University, G.C., Chamran Highway, Tehran, Iran.Associate Professor, Department of Microbiology, Faculty of Biological Sciences, Shahid Beheshti University, G.C., Chamran Highway, Tehran, Iran.Background: Multidrug resistant K. pneumoniae, particularly the extended-spectrum β-lactamase (ESBL) producing strains, are often responsible for the failure of antibiotic treatment in nosocomial infections. Employing molecular methods to distinguish between ESBL and non-ESBL producing isolates can help quick identification of these multidrug resistant pathogens and thereby initiating appropriate antibiotic therapy. The aim of this study was to employ RAPD-PCR to distinguish the genetic fingerprints of ESBL producing clinical isolates of K. pneumoniae from ESBL negative strains. Materials and Methods: Antibacterial susceptibility of 104 K. pneumoniae clinical isolates was determined to 13 antibacterial agents by disc diffusion. ESBL production was measured by the double disc synergy test followed by phenotypic confirmatory tests. Genetic fingerprinting was carried out by RAPD-PCR. Results: All isolates were susceptible to imipenem. Antibiotic resistance rates were: piperacillin (100%), ceftazidime (62.5%), cefotaxime (57.6%), aztreonam (52.8%), cefepime (51.9%), kanamycin (50.9%), gentamicin (41.3%), ciprofloxacin (37.5%), nitrofurantoin (30.6%), nalidixic acid (22.1%), piperacillin/ tazobactam (21.1%) and amikacin (9.6%). ESBL production was observed in 14 isolates (13.4%). Genetic fingerprinting performed on 43 isolates (14 ESBL positive and 29 ESBL negative) by RAPD-PCR, showed that 46.5% of the isolates belonged to a single profile (genotype 1), of which, the majority (62.1%) were non-ESBL producers. Conclusion: RAPD-PCR results showed heterogeneity among the isolates. There was no association between ESBL production with any specific genetic fingerprint.https://jcdr.net/articles/PDF/5373/10651_CE(Ra)_F(Sh)_PF1(AJ_Sh)_PFA(AK)_PF2(PAG).pdfesblgenetic fingerprintingklebsiella pneumoniaemultidrug resistancenosocomial isolatesrapd-pcr
spellingShingle Fereshteh Eftekhar
Parvaneh Nouri
Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran
Journal of Clinical and Diagnostic Research
esbl
genetic fingerprinting
klebsiella pneumoniae
multidrug resistance
nosocomial isolates
rapd-pcr
title Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran
title_full Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran
title_fullStr Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran
title_full_unstemmed Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran
title_short Correlation of RAPD-PCR Profiles with ESBL Production in Clinical Isolates of Klebsiella pneumoniae in Tehran
title_sort correlation of rapd pcr profiles with esbl production in clinical isolates of klebsiella pneumoniae in tehran
topic esbl
genetic fingerprinting
klebsiella pneumoniae
multidrug resistance
nosocomial isolates
rapd-pcr
url https://jcdr.net/articles/PDF/5373/10651_CE(Ra)_F(Sh)_PF1(AJ_Sh)_PFA(AK)_PF2(PAG).pdf
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AT parvanehnouri correlationofrapdpcrprofileswithesblproductioninclinicalisolatesofklebsiellapneumoniaeintehran