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Infect. Immun., 06 1995, 2243-2247, Vol 63, No. 6
DH Brown, BA Miles and BS Zwilling
Growth of mycobacterial species is controlled by a gene, Bcg (candidate
Nramp). Bcg acts at the macrophage level and is thought to control some
aspect of macrophage priming for activation. Infection of Mycobacterium
bovis BCG-susceptible (Bcgs) mice with several different mycobacterial
species results in the growth of the microorganisms, while the growth of
the same organisms is controlled in BCG-resistant (Bcgr) mice. The capacity
of Bcg to control the growth of M. tuberculosis has not been extensively
explored. The purpose of this investigation, therefore, was to compare the
growth of M. tuberculosis in Bcgr and Bcgs mice. We found that the growth
of tubercule bacilli was different in the lungs and spleens of Bcgr and
Bcgs mice when they were inoculated with fewer then 10(3) CFU of the
mycobacterium. The differences in growth were more easily distinguished in
the lungs then in the spleens. The growth of the microorganisms in both
strains of mice peaked between 35 and 43 days, and a latent infection was
established by 65 days after infection. Activation of the
hypothalamic-pituitary-adrenal axis resulted in reactivation of the growth
of M. tuberculosis in both Bcgr and Bcgs mice. Greater numbers of tubercule
bacilli were isolated from lungs than from spleens following reactivation.
The utility of this mouse model in the study of the establishment of
latency and reactivation of M. tuberculosis is discussed.
Copyright © 1995, American Society for Microbiology
Growth of Mycobacterium tuberculosis in BCG-resistant and -susceptible mice: establishment of latency and reactivation
Department of Microbiology, Ohio State University, Columbus 43210, USA.
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