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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.
Naserpour Farivar, Taghi; Najafipour, Reza; Johari, Pouran; Aslanimehr, Masoumeh; Peymani, Amir; Jahani Hashemi, Hoasan; Mirzaui, Baman.
Affiliation
  • Naserpour Farivar T; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
  • Najafipour R; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
  • Johari P; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
  • Aslanimehr M; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
  • Peymani A; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
  • Jahani Hashemi H; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
  • Mirzaui B; Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Iran J Microbiol ; 6(5): 335-40, 2014 Oct.
Article in En | MEDLINE | ID: mdl-25848524
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Iran J Microbiol Year: 2014 Document type: Article Affiliation country: Iran Country of publication: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Iran J Microbiol Year: 2014 Document type: Article Affiliation country: Iran Country of publication: Iran