To explore a simple, rapid, and inexpensive way to identify Mycobacterium t
uberculosis complex culture, dot blot hybridization using IS6110 as the mar
ker was performed against 2788 known clinical isolates of mycobacteria incl
uding M. tuberculosis (n = 721), M. kansasii (177), M. marinum (10), M. avi
um complex (700), M. terrae complex (203), M. fortuitum (476), M. chelonae
(439), and other nonpigmented Runyon's Group IV mycobacteria (62). We found
that the sensitivity and specificity of the test were 94.3% and 100%, resp
ectively. When this method was evaluated in a laboratory blind study of 125
3 initially unknown clinical isolates, its sensitivity and specificity were
91.2% and 100%, respectively. Because this identification test is technica
lly simple, rapid, and can be done in batches, together with ifs high sensi
tivity and specificity, it is a cost-effective method for routine identific
ation of M. tuberculosis complex in laboratories of areas with a high incid
ence of tuberculosis. (C) 1999 Elsevier Science Inc.