Protective immunity to mycobacterial infection is incompletely understood b
ut probably involves the coordinated interaction of multiple cell types and
cytokines, With the aim of developing assays that might provide a surrogat
e measure of protective immunity, rye have investigated the use of recombin
ant mycobacteria carrying luciferase reporter enzymes to assess the effecti
veness of antimycobacterial immunity in model systems. Measurement of lumin
escence was shown to provide a rapid and simple alternative to the counting
of CFU as a means of monitoring mycobacterial viability. We describe optim
ization of a luciferase reporter strain of Mycobacterium tuberculosis and d
emonstrate its application for the study of mycobacterial interactions with
host cells in tissue culture and the rapid assessment of vaccine efficacy
in a murine model.