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Infect. Immun., 05 1995, 1739-1744, Vol 63, No. 5
RM Tsolis, AJ Baumler and F Heffron
The Salmonella typhimurium gene for Mn-cofactored superoxide dismutase
(sodA) was cloned by complementation of an Escherichia coli sodA sodB
mutant for growth on minimal medium. Sequence analysis revealed an open
reading frame of 618 bp encoding a polypeptide with 97% identity to E. coli
SodA. A S. typhimurium sodA mutant was created by allelic exchange and
tested for the ability to survive in the murine macrophage-like cell line
J774. Growth of bacteria under iron-limiting conditions, inactivation of
the Fur repressor, or expression of sodA from a plasmid resulted in
increased resistance to early killing by J774 cells, which was abolished in
the sodA mutant. These results suggest that resistance to the early
oxygen-dependent microbicidal mechanisms of phagocytes involves the SodA
gene product. The S. typhimurium sodA mutant was not significantly
attenuated in mice, however, which suggests that resistance to early
oxygen-dependent microbicidal mechanisms in vivo may play only a minor role
in Salmonella pathogenesis.
Copyright © 1995, American Society for Microbiology
Role of Salmonella typhimurium Mn-superoxide dismutase (SodA) in protection against early killing by J774 macrophages
Department of Molecular Microbiology and Immunology, Oregon Health Sciences University, Portland 97201, USA.
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