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.