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Infect. Immun., 05 1996, 1794-1799, Vol 64, No. 5
FC Bange, AM Brown and WR Jacobs Jr
The ability of slow-growing mycobacteria to replicate within host
mononuclear phagocytes is thought to be central to the pathogenesis of
mycobacterial infection. However, because of the lack of a mycobacterial
mutant defective for intracellular replication, it has not been possible to
test this hypothesis directly. Previously, we showed that a BCG leucine
auxotroph with a transposon disruption of the leuD gene is unable to grow
in mice. Here we demonstrate that this mutant is also incapable of
replicating within cultured macrophages in vitro. Complementation of the
leuD mutation with the leuCD genes of Escherichia coli restored wild-type
levels of growth in macrophages, establishing that the defect for
intracellular replication was due to leucine auxotrophy per se and not to a
polar effect of the transposon insertion on an adjacent gene. These results
suggest that the inability of the leucine auxotroph to grow in mice was due
to its sequestration, after phagocytosis, in an intracellular compartment
from which it could not obtain leucine.
Copyright © 1996, American Society for Microbiology
Leucine auxotrophy restricts growth of Mycobacterium bovis BCG in macrophages
Department of Microbiology and Immunology, Howard Hughes Medical Institute, Albert Einstein College of Medicine, Yeshiva University, Bronx, New York 10461, USA.
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