Selected article for: "Assay specificity and diagnostic tool"

Author: Terlizzi, Maria Elena; Massimiliano, Bergallo; Francesca, Sidoti; Sinesi, Franca; Rosangela, Vendrame; Stefano, Gambarino; Costa, Cristina; Rossana, Cavallo
Title: Quantitative RT Real Time PCR and indirect immunofluorescence for the detection of human parainfluenza virus 1, 2, 3
  • Cord-id: q5mgue5z
  • Document date: 2009_5_13
  • ID: q5mgue5z
    Snippet: Human parainfluenza viruses (HPIVs) are distributed worldwide and are involved mainly in the pathogenesis of respiratory tract infections. The development and optimization of three quantitative reverse transcription real time polymerase chain reactions (RT Real Time Qt-PCRs) and an indirect immunofluorescence (IFA) for the detection and quantitation of HPIV-1, -2 and -3 in clinical samples are described. Efficiency, sensitivity, specificity, inter- and intra-assay variability and turnaround time
    Document: Human parainfluenza viruses (HPIVs) are distributed worldwide and are involved mainly in the pathogenesis of respiratory tract infections. The development and optimization of three quantitative reverse transcription real time polymerase chain reactions (RT Real Time Qt-PCRs) and an indirect immunofluorescence (IFA) for the detection and quantitation of HPIV-1, -2 and -3 in clinical samples are described. Efficiency, sensitivity, specificity, inter- and intra-assay variability and turnaround time of the two methods were compared. These assays have been validated on 131 bronchoalveolar lavage specimens. Based on the results obtained, the molecular methods represent a valid and rapid tool for clinical management and should be included in diagnostic panels aimed to evaluate suspected respiratory tract infections.

    Search related documents:
    Co phrase search for related documents
    • acid extraction and low detection: 1, 2, 3, 4, 5
    • acid extraction and low detection limit: 1, 2
    • acid extraction and low sensitivity: 1