Rapid detection of Mycobacterium tuberculosis in contaminated BACTEC 12B broth cultures by testing with amplified Mycobacterium tuberculosis direct test

Citation
Xt. Zheng et al., Rapid detection of Mycobacterium tuberculosis in contaminated BACTEC 12B broth cultures by testing with amplified Mycobacterium tuberculosis direct test, J CLIN MICR, 39(10), 2001, pp. 3718-3720
Citations number
27
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
39
Issue
10
Year of publication
2001
Pages
3718 - 3720
Database
ISI
SICI code
0095-1137(200110)39:10<3718:RDOMTI>2.0.ZU;2-O
Abstract
Contamination of broth cultures of acid-fast bacilli (AFB) by bacterial spe cies other than Mycobacterium species frequently occurs. Many of these cont aminated cultures require redecontamination and reincubation before the app ropriate tests can be performed for identification, significantly affecting the turnaround time for reporting culture results. In this study, the Ampl ified Mycobacterium Tuberculosis Direct Test (MTD; Gen-Probe) was performed to detect the Mycobacterium tuberculosis complex (MTBC) in 125 BACTEC 12B broth cultures with positive growth indices. Among these, 41 grew non-AFB b acteria only, and all 41 were negative by the MTD. The remaining 84 bottles contained contaminated cultures that grew both AFB and other bacteria or y easts. Repeat decontamination and reincubation of these specimens required a mean time of 13 days (range, 3 to 40 days). The MTD results were positive for 10 samples, 9 of which were MTBC culture positive and I of which grew Myobacterium celatum, a species known to cross-react in the MTD. All cultur es growing other mycobacterial species were negative by the MTD. The result s of this study demonstrate that the MTD is both sensitive and specific in detecting MTBC in contaminated broth cultures and that, when used selective ly, the MTD can potentially rule in or out a diagnosis of MTBC as much as 1 2 days earlier than using nonamplified DNA probe testing alone can.