SlyA is a global transcriptional regulator of Salmonella genes. SlyA is essential for Salmonella pathogenesis, for growth within phagocytes, and for resistance to oxidative stress. SlyA is maximally expressed in stationary phase and in macrophages. The focus of this proposal is to discern the mechanism by which SlyA contributes to Salmonella pathogenesis and oxidative stress resistance. The three specific aims are: 1) to identify Sly-regulated genes, 2) to determine the role of SlyA-dependent genes in oxidative stress resistance, and 3) to perform a molecular analysis of slyA transcription and translation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI048622-01
Application #
6228300
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
2001-09-27
Project End
2003-09-26
Budget Start
2001-09-27
Budget End
2003-09-26
Support Year
1
Fiscal Year
2001
Total Cost
$189,325
Indirect Cost
Name
North Carolina State University Raleigh
Department
Microbiology/Immun/Virology
Type
Schools of Earth Sciences/Natur
DUNS #
City
Raleigh
State
NC
Country
United States
Zip Code
27695
Will, W Ryan; Bale, Denise H; Reid, Philip J et al. (2014) Evolutionary expansion of a regulatory network by counter-silencing. Nat Commun 5:5270
Fritsche, Gernot; Nairz, Manfred; Libby, Stephen J et al. (2012) Slc11a1 (Nramp1) impairs growth of Salmonella enterica serovar typhimurium in macrophages via stimulation of lipocalin-2 expression. J Leukoc Biol 92:353-9
Libby, Stephen J; Brehm, Michael A; Greiner, Dale L et al. (2010) Humanized nonobese diabetic-scid IL2rgammanull mice are susceptible to lethal Salmonella Typhi infection. Proc Natl Acad Sci U S A 107:15589-94