Literature DB >> 9854078

Performance characteristics of the BDProbeTec system for direct detection of Mycobacterium tuberculosis complex in respiratory specimens.

G E Pfyffer1, P Funke-Kissling, E Rundler, R Weber.   

Abstract

Strand displacement amplification (SDA) technology has been established in a fully automated system known as BDProbeTec. Target sequences of the insertion sequence IS6110 and the 16S rRNA gene are simultaneously amplified, which thus allows the detection of Mycobacterium tuberculosis complex and, as an additional option, of most Mycobacterium species. Detection occurs via a chemiluminescent microwell assay that employs the simultaneous hybridization and capture of SDA products with a biotinylated capture probe and an alkaline phosphatase detector probe. We have evaluated the performance of the BDProbeTec system in detecting M. tuberculosis complex by testing 799 respiratory specimens and comparing the results to those obtained by conventional diagnostic techniques, i.e. , microscopy and culture (solid and radiometric media). M. tuberculosis was cultivated from 41 specimens, of which 28 (68.4%) were smear positive and 13 (31.6%) were smear negative. The overall sensitivity of the SDA assay was 97.6% (for smear-positive specimens, 100%; for smear-negative specimens, 92.3%), and specificity was 95. 0%. After resolution of the discrepancies by studying the patients' clinical data, sensitivity and specificity were 97.9 and 96.5%, respectively, and positive and negative predictive values were 63.9 and 99.9%, respectively. These preliminary data demonstrate that the BDProbeTec system has promising performance characteristics with respiratory specimens and that it allows the detection of M. tuberculosis complex within hours.

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Year:  1999        PMID: 9854078      PMCID: PMC84189     

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  15 in total

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2.  Genotypic identification of mycobacteria by nucleic acid sequence determination: report of a 2-year experience in a clinical laboratory.

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4.  Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis.

Authors:  A Telenti; F Marchesi; M Balz; F Bally; E C Böttger; T Bodmer
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Authors:  C A Spargo; M S Fraiser; M Van Cleve; D J Wright; C M Nycz; P A Spears; G T Walker
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8.  Diagnostic value of the strand displacement amplification method compared to those of Roche Amplicor PCR and culture for detecting mycobacteria in sputum samples.

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9.  Detection and identification of Mycobacterium tuberculosis directly from sputum sediments by amplification of rRNA.

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Authors:  J Bennedsen; V O Thomsen; G E Pfyffer; G Funke; K Feldmann; A Beneke; P A Jenkins; M Hegginbothom; A Fahr; M Hengstler; G Cleator; P Klapper; E G Wilkins
Journal:  J Clin Microbiol       Date:  1996-06       Impact factor: 5.948

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Review 2.  Relevance of commercial amplification methods for direct detection of Mycobacterium tuberculosis complex in clinical samples.

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Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

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4.  Rapid-cycle PCR and fluorimetry for detection of mycobacteria.

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5.  Availability and use of molecular microbiological and immunological tests for the diagnosis of tuberculosis in europe.

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6.  Rapid detection of laboratory cross-contamination with Mycobacterium tuberculosis using multispacer sequence typing.

Authors:  Zoheira Djelouadji; Jean Orehek; Michel Drancourt
Journal:  BMC Microbiol       Date:  2009-03-03       Impact factor: 3.605

7.  Pyrosequencing identification of Mycobacterium tuberculosis W-Beijing.

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8.  Commercial nucleic-acid amplification tests for diagnosis of pulmonary tuberculosis in respiratory specimens: meta-analysis and meta-regression.

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  8 in total

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