Literature DB >> 9705443

Early detection of Mycobacterium tuberculosis in BACTEC cultures by ligase chain reaction.

E Tortoli1, F Lavinia, M T Simonetti.   

Abstract

The LCx Mycobacterium tuberculosis ligase chain reaction system (Abbott Diagnostic Division, Abbott Park, Ill.) was used to detect M. tuberculosis in 150 consecutive BACTEC vials on the day on which a positive growth index (GI) was recorded. By LCx, M. tuberculosis DNA was detected in BACTEC vials on average 2.6 days before the presence of acid-fast bacilli could be confirmed by microscopic examination. A total of 106 of 108 M. tuberculosis isolates were detected without centrifugation from bottles presenting very low GIs (average, 70; median, 33). No false-positive result was obtained from nontuberculous mycobacteria or from isolates with contaminants.

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Year:  1998        PMID: 9705443      PMCID: PMC105213     

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


  14 in total

1.  Evaluation of a commercial ligase chain reaction kit (Abbott LCx) for direct detection of Mycobacterium tuberculosis in pulmonary and extrapulmonary specimens.

Authors:  E Tortoli; F Lavinia; M T Simonetti
Journal:  J Clin Microbiol       Date:  1997-09       Impact factor: 5.948

2.  Use of Gen-Probe and Bactec for rapid isolation and identification of mycobacteria. Correlation of probe results with growth index.

Authors:  B A Body; N G Warren; A Spicer; D Henderson; M Chery
Journal:  Am J Clin Pathol       Date:  1990-03       Impact factor: 2.493

3.  The resurgence of tuberculosis: is your laboratory ready?

Authors:  F C Tenover; J T Crawford; R E Huebner; L J Geiter; C R Horsburgh; R C Good
Journal:  J Clin Microbiol       Date:  1993-04       Impact factor: 5.948

4.  The diagnostic usefulness of a DNA probe for Mycobacterium tuberculosis complex (Gen-Probe) in Bactec cultures versus other diagnostic methods.

Authors:  M Telenti; J F de Quirós; M Alvarez; M J Santos Rionda; M C Mendoza
Journal:  Infection       Date:  1994 Jan-Feb       Impact factor: 3.553

Review 5.  Multiple-drug-resistant tuberculosis: current aspects in industrialized countries, and future strategies.

Authors:  C Perronne
Journal:  Res Microbiol       Date:  1993-02       Impact factor: 3.992

6.  Clinical usefulness of detecting growth of Mycobacterium tuberculosis in positive Bactec phials using PCR.

Authors:  A Morris; L Reller; B Devlin
Journal:  J Clin Pathol       Date:  1994-02       Impact factor: 3.411

7.  Direct identification of Mycobacterium tuberculosis, Mycobacterium avium, and Mycobacterium intracellulare from amplified primary cultures in BACTEC media using DNA probes.

Authors:  E M Peterson; R Lu; C Floyd; A Nakasone; G Friedly; L M de la Maza
Journal:  J Clin Microbiol       Date:  1989-07       Impact factor: 5.948

8.  Identification of Mycobacterium tuberculosis and Mycobacterium avium-M. intracellulare directly from primary BACTEC cultures by using acridinium-ester-labeled DNA probes.

Authors:  K D Evans; A S Nakasone; P A Sutherland; L M de la Maza; E M Peterson
Journal:  J Clin Microbiol       Date:  1992-09       Impact factor: 5.948

9.  Rapid detection and identification of pathogenic mycobacteria by combining radiometric and nucleic acid probe methods.

Authors:  P D Ellner; T E Kiehn; R Cammarata; M Hosmer
Journal:  J Clin Microbiol       Date:  1988-07       Impact factor: 5.948

10.  Ability of PCR assay to identify Mycobacterium tuberculosis in BACTEC 12B vials.

Authors:  B A Forbes; K E Hicks
Journal:  J Clin Microbiol       Date:  1994-07       Impact factor: 5.948

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  2 in total

1.  Rapid detection of Mycobacterium tuberculosis in contaminated BACTEC 12B broth cultures by testing with Amplified Mycobacterium Tuberculosis Direct Test.

Authors:  X Zheng; M Pang; H D Engler; S Tanaka; T Reppun
Journal:  J Clin Microbiol       Date:  2001-10       Impact factor: 5.948

2.  Two liquid medium systems, mycobacteria growth indicator tube and MB redox tube, for Mycobacterium tuberculosis isolation from sputum specimens.

Authors:  L Heifets; T Linder; T Sanchez; D Spencer; J Brennan
Journal:  J Clin Microbiol       Date:  2000-03       Impact factor: 5.948

  2 in total

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