Literature DB >> 12710097

[Evaluation of Bactec MGIT 960 fluorescent method in diagnosis of tuberculosis].

Ewa Augustynowicz-Kopeć1, Albert Jaworski, Zofia Zwolska.   

Abstract

We evaluated the fluorescent Bactec MGIT 960 the new system in Poland, which is a fully automated, non-invasive, system for growth and detection of Mycobacterium with a capacity to incubate and continuously monitor 960 of 7-ml culture tubes. This system is equipped with special oxygen-quenching fluorescent sensor, which permits to continuously monitoring of microbial growth. Processed specimens were inoculated into Bactec MGIT 960, Bactec 460 Tb and MB/BacT as well as on to Lowenstein-Jensen slants. The greatest number of isolates of M. tuberculosis complex was recovered by using Bactec MGIT 960 system (49/19.5%). Other systems detected M. tuberculosis complex as follows: Bactec 460 Tb (47/18.7%), MB/BacT (43/17/1%), L-J (38/15.1%). Detection mean time of mycobacterial growth in smear-positive specimens were 15.4 days for Bactec MGIT 960, 16.2 days for Bactec 460 Tb, 15.1 days for MB/BacT and 28.2 days for L-J medium The rates of contamination for each of the system were: 3.8% for Bactec MGIT 960 and Bactec 460 Tb, 3.6% for MB/BacT and 2.9% for L-J. In conclusion Bactec MGIT 960 system is a valuable alternative of radiometric, semi automated Bactec 460 Tb system.

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Year:  2002        PMID: 12710097

Source DB:  PubMed          Journal:  Pneumonol Alergol Pol        ISSN: 0867-7077


  2 in total

1.  Meta-analysis of BACTEC MGIT 960 and BACTEC 460 TB, with or without solid media, for detection of mycobacteria.

Authors:  M Cruciani; C Scarparo; M Malena; O Bosco; G Serpelloni; C Mengoli
Journal:  J Clin Microbiol       Date:  2004-05       Impact factor: 5.948

2.  Comparison of the conventional culture, the manual fluorescent MGIT system and the automated fluorescent MGIT 960 culture system for the detection of Mycobacterium avium ssp. avium in tissues of naturally infected hens.

Authors:  E J Shitaye; V Beran; J Svobodová; M Morávková; V Babák; I Pavlík
Journal:  Folia Microbiol (Praha)       Date:  2009-05-06       Impact factor: 2.099

  2 in total

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