Title of article :
Development and evaluation of a Quadruplex Taq Man real-time PCR assay for simultaneous detection of clinical isolates of Enterococcus faecalis, Enterococcus faecium and their vanA and vanB genotypes.
Author/Authors :
Naserpour Farivar، Taghi نويسنده , , Najafipour، Reza نويسنده Cellular and Molecular Research Centre, Qazvin University of Medical Sciences, Qazvin, Iran , , Johari، Pouran نويسنده Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, IR Iran , , Aslanimehr، Masoumeh نويسنده Cellular and Molecular Research Centre, Qazvin University of Medical Sciences, Qazvin, IR Iran , , Peymani، Amir نويسنده Microbiology Department, Infectious and Tropical Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran , , Jahani Hashemi، Hoasan نويسنده Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran. Jahani Hashemi, Hoasan , Mirzaui، Baman نويسنده Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran. Mirzaui, Baman
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2014
Pages :
6
From page :
335
To page :
340
Abstract :

Background and Objectives: We developed and evaluated the utility of a quadruplex Taqman real-time PCR assay that allows simultaneous identification of vancomycin-resistant genotypes and clinically relevant enterococci.
Materials and Methods: The specificity of the assay was tested using reference strains of vancomycin-resistant and susceptible enterococci. In total, 193 clinical isolates were identified and subsequently genotyped using a Quadruplex Taqman real-time PCR assay and melting curve analysis. Representative Quadruplex Taqman real-time PCR amplification curve were obtained for Enterococcus faecium, Enterococcus faecalis, vanA-containing E. faecium, vanB-containing E. faecalis.
Results: Phenotypic and genotypic analysis of the isolates gave same results for 82 enterococcal isolates, while in 5 isolates, they were inconsistent. We had three mixed strains, which were detected by the TaqMan real-time PCR assay and could not be identified correctly using phenotypic methods.
Conclusion: Vancomycin resistant enterococci (VRE) genotyping and identification of clinically relevant enterococci were rapidly and correctly performed using TaqMan real-time multiplex real-time PCR assay.

Journal title :
IJM Iranian Journal of Microbiology
Serial Year :
2014
Journal title :
IJM Iranian Journal of Microbiology
Record number :
2390577
Link To Document :
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