IFN-γ plays a detrimental role in murine defense against nasal colonization of Staphylococcus aureus

Immunology Letters

Volumn 123, Issue 2, 2009, Pages 185-188

  Satorres, Sara Elena ^a   Alcaráz, Lucía Esther ^a   Cargnelutti, Ethelina ^a,b   Di Genaro, Maria Silvia ^a,b  

^a Chemistry   (Argentina)

^b CONICET ^*  (Argentina)

Author keywords

IFN ; Nasal colonization; Slime production; Staphylococcus aureus

Indexed keywords

GAMMA INTERFERON; IMMUNOGLOBULIN A; INTERLEUKIN 12P40; SODIUM CHLORIDE;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; BACTERIAL COLONIZATION; BACTERIAL COUNT; BACTERIAL INFECTION; BACTERIAL STRAIN; BAGG ALBINO MOUSE; C57BL 6 MOUSE; CELL COUNT; COLONY FORMING UNIT; COMPARATIVE STUDY; CONTROLLED STUDY; IMMUNE RESPONSE; IMMUNITY; LUNG; MALE; MOUSE; NONHUMAN; NOSE MUCOSA; PRIORITY JOURNAL; STAPHYLOCOCCUS AUREUS; WILD TYPE;

ANIMALS; INTERFERON-GAMMA; INTERLEUKIN-12 SUBUNIT P40; INTERLEUKIN-4; MALE; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MICE, KNOCKOUT; NOSE; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS AUREUS;

EID: 67349288505     PISSN: 01652478     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.imlet.2009.03.003     Document Type: Article

References (24)

1. Lecomte F., Nouvellon M., and Levesque H. Nasal carriage of Staphylococcus aureus. N Eng J Med 344 (2001) 1399-1400
2. Kevin B., Kiser J.M., Cantey-Kiser, and Lee J.C. Development and characterization of a Staphylococcus aureus nasal colonization model in mice. Infect Immun 67 (1999) 5001-5006
3. Sanford B.A., Thomas V.L., and Ramsay M.A. Binding of staphylococci to mucus in vivo and in vitro. Infect Immun 57 (1989) 3735-3742
4. Cheung A.L., Bayer A.S., Zhang G., Gresham H., and Xiong Y.Q. Regulation of virulence determinants in vitro and in vivo in Staphylococcus. FEMS Immunol Med Microbiol 40 (2004) 1-9
5. Donlan R.M., and Costerton J.W. Biofilms: survival mechanisms of clinically relevant microorganisms. Clin Microbiol Rev 15 (2002) 167-193
6. Götz F. Staphylococcus and biofilms. Mol Microbiol 43 (2002) 1367-1378
7. Bruno Gonzalez Z., Senna J.P.M., Fiette L., Shorte S., Testard A., Chignard M., et al. Bacterial and host factors implicated in nasal carriage of methicillin-resistant Staphylococcus aureus in mice. Infect Immun 73 (2005) 1847-1851
8. Nakane A., Okamoto M., Asano M., Kohanawa M., and Minagawa T. Endogenous gamma interferon, tumor necrosis factor, and interleukin-6 in Staphylococcus aureus infection in mice. Infect Immun 63 (1995) 1165-1172
9. McLoughlin R.M., Lee J.C., Kasper D.L., and Tzianabos A.O. IFN-γ regulated chemokine production determines the outcome of Staphylococcus aureus infection. J Immunol 181 (2008) 1323-1332
10. Freeman D.J., Falkiner F.R., and Keane C.T. New method for detecting slime production by coagulase-negative staphylococci. J Clin Pathol 42 (1989) 872-874
11. Arciola C.R., Baldassari L., and Montanaro L. In catherer infections by Staphylococcus epidermidis the intercellular adhesion (ica) locus is a molecular marker of the virulent slime-producing strains. J Biomed Mater Res 59 (2002) 557-562
12. Satorres S.E., Alcaraz L., and Di Genaro M.S. Association between high IL-8 levels and Staphylococcus aureus-specific IgA antibodies in subjects with type I diabetes mellitus from Argentina. Diab Res Clin Pract 77 (2007) 489-491
13. Autenrieth I.B., Beer M., Bohn E., Kauffman S.H., and Heesemann J. Immune response to Yersinia enterocolitica in susceptible BALB/c and resistant C57BL/6 mice: an essential role for gamma interferon. Infect Immun 62 (1994) 2590-2599
14. Zhao Y.X., Nilsson L.M., and Tarkowski. The dual role of interferon-γ in experimental Staphylococcus aureus septicaemia versus arthritis. Immunology 93 (1998) 80-85
15. Boelens J.J., Poll T., Dankert J., and Zaat S.A. Interferon-γ protects against biomaterial-associated Staphylococcus epidermidis infection in mice. J Infect Dis 181 (2000) 1167-1171
16. Nasaki S., Nishikawa S., Miuria T., Mizuki M., Yomada K., Madarame H., et al. Interleukin-4 and interleukin-10 are involved in host resistance to Staphylococcus aureus infection through regulation of gamma interferon. Infect Immun 68 (2000) 2424-2430
17. Hoeve M.A., Savage N.D., de Boer T., Langenberg D.M., de Waal Malefyt R., Ottenhoff T.H., et al. Divergent effects of IL-12 and IL-23 on the production of IL-17 by human T cells. Eur J Immunol 36 (2006) 661-670
18. Layh-Schmit G., and Colbert R.A. The interlukin-23/interlukin-17 axis in spondyloarthritis. Curr Opin Rheumatol 20 (2008) 392-397
19. Aujla S.J., Dubin P.J., and Kolls J.K. Th17 cells and mucosal host defense. Sem Immunol 19 (2007) 377-382
20. Smits H.H., van Beelen A.J., Hessle C., Westland R., de Jong E., Soeteman E., et al. Commensal Gram-negative bacteria prime human dendritic cells for enhance Th1 development. Eur J Immunol 34 (2004) 1371-1380
21. Sun K., Salmon S.L., Lotz S.A., and Metzger D.W. Interleukin-12 promotes γ interferon-dependent neutrophil recruitment in the lung and improves protection against respiratory Streptococcus pneumoniae infection. Infect Immun 75 (2007) 1196-1202
22. Kugathasan S., Saubermann L.J., Smith L., Kou D., Itoh J., Binion D.G., et al. Mucosal T-cell immunoregulation varies in early and late inflammatory bowel disease. Gut 56 (2007) 1696-1705
23. Ellis T.N., and Beaman B.L. Interferon-γ activation of polymorphonuclear neutrophil function. Immunology 112 (2004) 2-12
24. Lee W.L., and Downey G.P. Neutrophil activation and acute lung injury. Curr Opin Crit Care 7 (2001) 1-7