RAPID IDENTIFICATION OF MYCOBACTERIA BY THE GEN-PROBE ACCUPROBE SYSTEM

Citation
R. Lumb et al., RAPID IDENTIFICATION OF MYCOBACTERIA BY THE GEN-PROBE ACCUPROBE SYSTEM, Pathology, 25(3), 1993, pp. 313-315
Citations number
19
Categorie Soggetti
Pathology
Journal title
ISSN journal
00313025
Volume
25
Issue
3
Year of publication
1993
Pages
313 - 315
Database
ISI
SICI code
0031-3025(1993)25:3<313:RIOMBT>2.0.ZU;2-Y
Abstract
Chemiluminescent acridinium ester-labelled (AE)-DNA probes (Gen-Probe, Inc., San Diego, Calif.) for the identification of Mycobacterium tube rculosis complex (MTBC) and the M. avium-M. intracellulare complex (MA C) were evaluated using 184 mycobacterial isolates cultured in BACTEC 12B vials (Becton Dickinson and Co., Towson, Md.). A 1.5 mt aliquot fr om BACTEC 12B vials containing acid-fast bacilli and a Growth Index of > 200 was concentrated 15-fold using a centrifugation step prior to p erforming the test procedure. When 184 mycobacterial isolates were tes ted (42MTBC/142 nontuberculous mycobacteria) using the AE-MTBC probe, there was 100% sensitivity and specificity when compared with conventi onal identification procedures. Criteria for using the AE-MAC probe we re defined to optimize results whilst minimizing laboratory costs. Nin ety-one (64%) of AE-MTBC probe negative isolates failed to meet select ion criteria and were not tested. When 51 (36%) of the AE-MTBC-probe n egative mycobacterial isolates were tested, the AE-MAC probe was found to be 88% sensitive and 100% specific. The nonisotopic Gen-Probe test is a rapid and practical alternative to current procedures for differ entiation of mycobacteria.