Salmonella Enterica serovar Typhimurium HilA-LacZY fusion gene response to iron chelation or supplementation in rich and minimal media

Journal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes

Volumn 39, Issue 5-6, 2004, Pages 861-870

  Rishi, P ^a   Woodward, C L ^b   Kim, W K ^b   Ricke, S C ^b  

^a PANJAB UNIVERSITY   (India)

^b TEXAS A AND M UNIVERSITY   (United States)

Author keywords

Expression; HilA gene; Iron; Salmonella Typhimurium

Indexed keywords

ASSAYS; CHELATION; ENZYMES; GENES; IRON;

BRAIN HEART INFUSION (BHI); CHELATORS; FUSION STRAINS; MILLER UNITS;

MICROORGANISMS;

2,2' BIPYRIDINE; BETA GALACTOSIDASE; FERROZINE; IRON; VIRULENCE FACTOR;

GENETIC VARIATION; IRON; VIRULENCE;

ARTICLE; BACTERIAL GENE; BACTERIAL VIRULENCE; CONTROLLED STUDY; CULTURE MEDIUM; ENZYME ACTIVITY; FUSION GENE; GASTROENTERITIS; GENE EXPRESSION; HILA GENE; IRON CHELATION; IRON THERAPY; NONHUMAN; SALMONELLA ENTERICA; SEROTYPE;

ACRONICTA LEPORINA; BACTERIA (MICROORGANISMS); NEGIBACTERIA; SALMONELLA ENTERICA; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHIMURIUM; SALMONELLA TYPHIMURIUM; TYPHIMURIUM;

EID: 9744283471     PISSN: 03601234     EISSN: None     Source Type: Journal    
DOI: 10.1081/LESB-200030894     Document Type: Article

References (26)

1. El-Gazzar, F.E.; Marth, E.H. Salmonellae, salmonellosis, and dairy foods. A review. J. Dairy. Sci. 1992, 75, 2327-2343.
2. Collazo, C.M.; Galán, J.E. Requirement for exported proteins in secretion through the invasion associated type III system of Salmonella typhimurium. Infect. Immun. 1996, 64, 3524-3531.
3. Galán, J.E. Molecular genetic bases of Salmonella entry into host cells. Mol. Microbiol. 1996, 20, 263-271.
4. Lee, C.A.; Jones, B.D.; Falkow, S. Identification of a Salmonella typhimurium invasion locus by selection for hyperinvasive mutants. Proc. Natl. Acad. Sci. USA 1992, 89, 1847-1851.
5. Bajaj, V.; Hwang, C.; Lee, C.A. hilA is a novel ompR/toxR family member that activates the expression of Salmonella typhimurium invasion genes. Mol. Microbiol. 1995, 18, 715-727.
6. Penheiter, K.L.; Mathur, N.; Giles, D.; Fahlen, T.; Jones, B.D. Non-invasive Salmonella typhimurium mutants are avirulent because of an inability to enter and destroy M cells of ileal Peyer's patches. Mol. Microbiol. 1997, 24, 697-709.
7. Bajaj, V.; Lucas, L.; Hwang, C.; Lee, C.A. Co-ordinate regulation of Salmonella typhimurium invasion genes by environmental and regulatory factors is mediated by control of hilA expression. Mol. Microbiol. 1996, 22, 703-714.
8. Mekalanos, J.J. Environmental signals controlling expression of virulence determinants in bacteria. J. Bacteriol. 1992, 174, 1-7.
9. Otto, B.R.; Verweij-van Vught, A.M.J.J.; MacLaren, D.M. Transferrins and heme compounds as iron source for pathogenic bacteria. Crit. Rev. Microbiol. 1992, 18, 217-233.
10. Bäumler, A.J.; Tsolis, R.M.; Fitch, T.A.; Adams, L.G. Evolution of host adaptation in Salmonella enterica. Infect. Immun. 1998, 66, 4579-4587.
11. Sood, S.; Rishi, P.; Sharma, S.; Sapru, S.; Ganguly, N.K. Expression of iron regulated outermembrane protein in Salmonella. typhi grown on solid media. Med. Sci. Res. 1999, 27, 6-13.
12. Galhardo, R.S.; Almeida, C.E.B.; Leitão, A.C.; Cabral-Neto, J.B. Repair of DNA lesions induced by hydrogen peroxide in the presence of iron chelators in Escherichia coli: participation of endonuclease IV and Fpg. J. Bacteriol. 2000, 182, 1964-1968.
13. Baillon, M.-L.A.; Arnoud, H.M.; van Vliet, V.; Ketley, J.M.; Constantinidou, C.; Penn, C.W. An iron regulated alkyl hydroperoxide reductase (AhpC) confers aerotolerance and oxidative stress resistance to the microaerophilic pathogen Compylobacter jejuni. J. Bacteriol. 1999, 181, 4798-4804.
14. Carter, P. Spectrophotometric determination of serum iron at the submicrogram level with a new reagent (Ferrozine). Anal. Biochem. 1971, 40, 450-458.
15. Miller, J.H. Experiments in Molecular Genetics; Cold Spring Harbor Laboratory Press: Cold Spring Harbor, N.Y., 1972.
16. Payne, S.M. Iron and virulence in the family enterobacteriaceae. Crit. Rev. Microbiol. 1988, 16, 81-111.
17. Klebba, P.E.; McIntosh, M.A.; Neilands, J.B. Kinetics of biosynthesis of iron-regulated membrane protein in E. coli. J. Bacteriol. 1982, 149, 880-888.
18. Griffiths, E. Availability of iron and survival of bacteria in infection. In Med. Microbiol; Easmon, C.S.F., Jeljasewicz, J., Brown, M.R.K.I., Lambert, P.A., Eds.; Academic Press Inc.: London, 1983; Vol. 3, 153-177.
19. Fernandez-Beros, M.E.; Gonzalez, C.; McIntosh, M.A.; Cabello, F.C. Immune response to the iron deprivation induced proteins of S. typhi in typhoid fever. Infect. Immun. 1989, 57, 1271-1275.
20. Harkness, R.E.; Chong, P.; Klein, M. Identification of two iron-repressed periplasmic proteins in Haemophilus influenzae. J. Bacteriol. 1992, 174, 2425-2430.
21. Nutt, J.D.; Medvedev, K.L.; Woodward, C.L.; Pillai, S.D.; Ricke, S.C. Assessment of laboratory media controls for determining Salmonella virulence potential of poultry water sources using a hilA:lacZY fusion strain. J. Rap. Meth. Auto. Microbiol. 2002, 10, 173-184.
22. Loeb, L.A.; James, E.A.; Waltersdorph, A.M.; Klebanoff, S.J. Mutagenesis by the autoxidation of iron with isolated DNA. Proc. Natl. Acad. Sci. USA 1988, 85, 3918-3922.
23. Chen, H.; Anantheswaran, R.C.; Knabel, S.J. Optimization of iron supplementation for enhanced detection of Salmonella enteritidis in eggs. J. Food. Prot. 2001, 64, 1279-1285.
24. Asad, N.R.; Leitão, A.C. Effects of metal ion chelators on DNA strand breaks and inactivation produced by hydrogen peroxide in Escherichia coli: Detection of iron-independent lesions. J. Bacteriol. 1991, 173, 2562-2568.
25. Foster, J.W.; Hall, H.K. Effect of Salmonella typhimurium ferric uptake regulator (fur) mutations on iron and pH-regulated protein synthesis. J. Bacteriol. 1992, 174, 4317-4323.
26. Tsolis, R.M.; Bäumler, A.J.; Heffron, F.; Stojiljcovic, I. Contribution of TonB- and Feo-mediated iron uptake to growth of Salmonella typhimurium in the mouse. Infect. Immun. 1996, 64, 4549-4556.