Journal of Leukocyte Biology 47:25-30 (1990) © 1990 Wiley-Liss, Inc. Killing of Mycobacterium smegmatis by Macrophages From Genetically Susceptible and Resistant Mice

The bactericidal function of macrophages was investigated in congenic mice expressing the phenotype of susceptibility (B10.A, BcgM) or resistance (B10.A.Bcg’) to mycobacterial infection. When spienic and peritoneai macrophages from these two mouse strains were infected in vitro with Mycobacterium smegmatis, the Sd macrophages were shown to inactivate M. smegmatis more efficiently than their Bc? congenic counterparts. The mechanisms of this superior antimycobacterial activity was studied further. Addition of catalase did not abolish killing to a significant degree in either allelic type of macrophage, suggesting that hydrogen peroxide production was not involved In the killing activity controlled by the Bcg gene. Activation of Bc? macrophages by exposure to crude lym-phokmnes rendered them equally as efficient as their Bcgr counterparts in their capacity to destroy M. smegmatis. This finding suggests that both the genetically resistant and susceptible macrophages have the potential to kill M. smegmatis in vitro. This potential is expressed constitutively by the Bcgr but not Bc? macrophages and can be induced, by lymphokmne treatment, in the Bc? macrophages. In a final set of experiments, the macrophage killing of M. smegmatis was evaluated as a test system to type for the Bcg gene ailelic type in vitro, using a set of AXB and BXA recombinant inbred strains of mice. Results obtained show that typing of AXB/BXA recombinant inbred strains for the trait of bactericidal activity vs. M. smegmatls in vitro revealed a perfect match with the strain distribution pattern of resistance/susceptibility to Mycobacterium bovis BCG in vivo. Key words: Bcg gene, macrophage activation, macrophage bactericidal functio