Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. II. Effects on microbial proliferation and host survival in vivo

Citation
P. Mastroeni et al., Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. II. Effects on microbial proliferation and host survival in vivo, J EXP MED, 192(2), 2000, pp. 237-247
Citations number
59
Categorie Soggetti
Medical Research General Topics
Journal title
JOURNAL OF EXPERIMENTAL MEDICINE
ISSN journal
00221007 → ACNP
Volume
192
Issue
2
Year of publication
2000
Pages
237 - 247
Database
ISI
SICI code
0022-1007(20000717)192:2<237:AAOTNP>2.0.ZU;2-B
Abstract
The roles of the NADPH phagocyte oxidase (phox) and inducible nitric oxide synthase (iNOS) in host resistance to Virulent Salmonella typhimurium were investigated in gp91phox(-/-), iNOS(-/-), and congenic wild-type mice. Alth ough both gp91phox(-/-) and iNOS(-/-) mice demonstrated Increased susceptib ility to infection with S. typhimurim compared with wild-type mice, the kin etics of bacterial replication were dramatically different in the gp91phox( -/-) and iNOS(-/-) mouse strains. Greater bacterial numbers were present in the spleens and livers of gp91phox(-/-) mice compared with C57BL/6 control s as early as day 1 of infection, and all of the gp91phox(-/-) mice succumb ed to infection within 5 d. In contrast, an increased bacterial burden was detected within reticuloendothelial organs of iNOS(-/-) mice only beyond th e first week of infection. Influx of inflammatory CD11b(+) cells, granuloma formation, and serum interferon gamma levels were unimpaired in iNOS(-/-) mice, but the iNOS-deficient granulomas were unable to limit bacterial repl ication. The NADPH phagocye oxidase and iNOS are both required for host res istance to wild-type Salmonella, but appear to operate principally at diffe rent stages of infection.