Transcriptional regulation of Salmonella enterica serovar Typhimurium genes by bile

FEMS Immunology and Medical Microbiology

Volumn 41, Issue 2, 2004, Pages 177-185

  Prouty, A M ^a   Brodsky, I E ^b   Manos, J ^c   Belas, R ^c   Falkow, S ^b   Gunn, J S ^a,d  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF MARYLAND   (United States)

^d OHIO STATE UNIVERSITY   (United States)

Author keywords

Bile; Microarray; Salmonella; Transcription

Indexed keywords

BACTERIAL DNA;

ARTICLE; BACTERIAL GENE; BILE; BIOSYNTHESIS; CONTROLLED STUDY; DNA FINGERPRINTING; DNA MICROARRAY; EPITHELIUM CELL; GENE EXPRESSION; GENE REPRESSION; INTESTINE MOTILITY; MASS SPECTROMETRY; NONHUMAN; OPERON; PRIORITY JOURNAL; PROTEIN SYNTHESIS; SALMONELLA ENTERICA; TRANSCRIPTION INITIATION; TRANSCRIPTION REGULATION; TWO DIMENSIONAL GEL ELECTROPHORESIS; VIRULENCE;

BACTERIAL PROTEINS; BILE; CELL MOVEMENT; DNA, BACTERIAL; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; FLAGELLA; GENE EXPRESSION REGULATION, BACTERIAL; HUMANS; MEMBRANE PROTEINS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; RECOMBINATION, GENETIC; RNA, BACTERIAL; SALMONELLA INFECTIONS; SALMONELLA TYPHIMURIUM; TRANSCRIPTION, GENETIC;

EID: 2442507109     PISSN: 09288244     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.femsim.2004.03.002     Document Type: Article

References (49)

1. Gunn J.S. Mechanisms of bacterial resistance and response to bile. Microbes Infect. 2:2000;907-913
2. Nikaido H. Outer membrane of Salmonella typhimurium. Transmembrane diffusion of some hydrophobic substances. Biochim. Biophys. Acta. 433:1976;118-132
3. Sukupolvi S., Vaara M. Salmonella typhimurium and Escherichia coli mutants with increased outer membrane permeability to hydrophobic compounds. Biochim. Biophys. Acta. 988:1989;377-387
4. Gupta S., Chowdhury R. Bile affects production of virulence factors and motility of Vibrio cholerae. Infect. Immun. 65:1997;1131-1134
5. Pope L.M., Reed K.E., Payne S.M. Increased protein secretion and adherence to HeLa cells by Shigella spp. following growth in the presence of bile salts. Infect. Immun. 63:1995;3642-3648
6. Prouty A.M., Gunn J.S. Salmonella enterica serovar Typhimurium invasion is repressed in the presence of bile. Infect. Immun. 68:2000;6763-6769
7. Schuhmacher D.A., Klose K.E. Environmental signals modulate ToxT-dependent virulence factor expression in Vibrio cholerae. J. Bacteriol. 181:1999;1508-1514
8. Van Velkinburgh J.C., Gunn J.S. PhoP-PhoQ-regulated loci are required for enhanced bile resistance in Salmonella spp. Infect. Immun. 67:1999;1614-1622
9. Halliday C.E., Inge P.M., Farthing M.J. Characterization of bile salt uptake by Giardia lamblia. Int. J. Parasitol. 25:1995;1089-1097
10. Prouty A.M., Van Velkinburgh J.C., Gunn J.S. Salmonella enterica serovar Typhimurium resistance to bile: identification and characterization of the tolQRA cluster. J. Bacteriol. 184:2002;1270-1276
11. Dussurget O., Cabanes D., Dehoux P., Lecuit M., Buchrieser C., Glaser P., Cossart P. Listeria monocytogenes bile salt hydrolase is a PrfA-regulated virulence factor involved in the intestinal and hepatic phases of listeriosis. Mol. Microbiol. 45:2002;1095-1106
12. Prouty A.M., Brodsky I.E., Falkow S., Gunn J.S. Bile-salt-mediated induction of antimicrobial and bile resistance in Salmonella typhimurium. Microbiology. 150:2004;775-783
13. Prouty A.M., Schwesinger W.H., Gunn J.S. Biofilm formation and interaction with the surfaces of gallstones by Salmonella spp. Infect. Immun. 70:2002;2640-2649
14. Dutta U., Garg P.K., Kumar R., Tandon R.K. Typhoid carriers among patients with gallstones are at increased risk for carcinoma of the gallbladder. Am. J. Gastroenterol. 95:2000;784-787
15. Lai C.W., Chan R.C., Cheng A.F., Sung J.Y., Leung J.W. Common bile duct stones: a cause of chronic salmonellosis. Am. J. Gastroenterol. 87:1992;1198-1199
16. Gunn J.S., Miller S.I. PhoP-PhoQ activates transcription of pmrAB, encoding a two-component regulatory system involved in Salmonella typhimurium antimicrobial peptide resistance. J. Bacteriol. 178:1996;6857-6864
17. Gunn J.S., Hohmann E.L., Miller S.I. Transcriptional regulation of Salmonella virulence: a PhoQ periplasmic domain mutation results in increased net phosphotransfer to PhoP. J. Bacteriol. 178:1996;6369-6373
18. Simons R.W., Houman F., Kleckner N. Improved single and multicopy lac-based cloning vectors for protein and operon fusions. Gene. 53:1987;85-96
19. Elliott T. A method for constructing single-copy lac fusions in Salmonella typhimurium and its application to the hemA-prfA operon. J. Bacteriol. 174:1992;245-253
20. Datsenko K.A., Wanner B.L. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc. Natl. Acad. Sci. USA. 97:2000;6640-6645
21. O'Farrell P.H. High resolution two-dimensional electrophoresis of proteins. J. Biol. Chem. 250:1975;4007-4021
22. Henzel W.J., Billeci T.M., Stults J.T., Wong S.C., Grimley C., Watanabe C. Identifying proteins from two-dimensional gels by molecular mass searching of peptide fragments in protein sequence databases. Proc. Natl. Acad. Sci. USA. 90:1993;5011-5015
23. Mann M., Hojrup P., Roepstorff P. Use of mass spectrometric molecular weight information to identify proteins in sequence databases. Biol. Mass Spectrom. 22:1993;338-345
24. Eisen M.B., Brown P.O. DNA arrays for analysis of gene expression. Methods Enzymol. 303:1999;179-205
25. Chan K., Baker S., Kim C.C., Detweiler C.S., Dougan G., Falkow S. Genomic comparison of Salmonella enterica serovars and Salmonella bongori by use of an S. enterica serovar Typhimurium DNA microarray. J. Bacteriol. 185:2003;553-563
26. Tusher V.G., Tibshirani R., Chu G. Significance analysis of microarrays applied to the ionizing radiation response. Proc. Natl. Acad. Sci. USA. 98:2001;5116-5121
27. Sperandio V., Torres A.G., Giron J.A., Kaper J.B. Quorum sensing is a global regulatory mechanism in enterohemorrhagic Escherichia coli O157:H7. J. Bacteriol. 183:2001;5187-5197
28. Miller V.L., Beer K.B., Loomis W.P., Olson J.A., Miller S.I. An unusual pagC::TnphoA mutation leads to an invasion- and virulence-defective phenotype in Salmonellae. Infect. Immun. 60:1992;3763-3770
29. Gunn J.S., Alpuche-Aranda C.M., Loomis W.P., Belden W.J., Miller S.I. Characterization of the Salmonella typhimurium pagC/pagD chromosomal region. J. Bacteriol. 177:1995;5040-5047
30. Court D., Huang T.F., Oppenheim A.B. Deletion analysis of the retroregulatory site for the lambda int gene. J. Mol. Biol. 166:1983;233-240
31. de Kort G., Bolton A., Martin G., Stephen J., van de Klundert J.A. Invasion of rabbit ileal tissue by Enterobacter cloacae varies with the concentration of OmpX in the outer membrane. Infect. Immun. 62:1994;4722-4726
32. Miller V.L., Falkow S. Evidence for two genetic loci in Yersinia enterocolitica that can promote invasion of epithelial cells. Infect. Immun. 56:1988;1242-1248
33. Miller V.L., Farmer 3rd J.J., Hill W.E., Falkow S. The ail locus is found uniquely in Yersinia enterocolitica serotypes commonly associated with disease. Infect. Immun. 57:1989;121-131
34. Miller V.L., Bliska J.B., Falkow S. Nucleotide sequence of the Yersinia enterocolitica ail gene and characterization of the Ail protein product. J. Bacteriol. 172:1990;1062-1069
35. Vogt J., Schulz G.E. The structure of the outer membrane protein OmpX from Escherichia coli reveals possible mechanisms of virulence. Struct. Fold Des. 7:1999;1301-1309
36. Pulkkinen W.S., Miller S.I. A Salmonella typhimurium virulence protein is similar to a Yersinia enterocolitica invasion protein and a bacteriophage lambda outer membrane protein. J. Bacteriol. 173:1991;86-93
37. Miller V.L., Beer K.B., Heusipp G., Young B.M., Wachtel M.R. Identification of regions of Ail required for the invasion and serum resistance phenotypes. Mol. Microbiol. 41:2001;1053-1062
38. Robbe-Saule V., Coynault C., Ibanez-Ruiz M., Hermant D., Norel F. Identification of a non-haem catalase in Salmonella and its regulation by RpoS (sigmaS). Mol. Microbiol. 39:2001;1533-1545
39. Ibanez-Ruiz M., Robbe-Saule V., Hermant D., Labrude S., Norel F. Identification of RpoS (sigma(S))-regulated genes in Salmonella enterica serovar Typhimurium. J. Bacteriol. 182:2000;5749-5756
40. Hueck C.J. Type III protein secretion systems in bacterial pathogens of animals and plants. Microbiol. Mol. Biol. Rev. 62:1998;379-433
41. 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. 89:1992;1847-1851
42. Kim C.C., Falkow S. Significance analysis of lexical bias in microarray data. BMC Bioinform. 4:2003;12
43. Chilcott G.S., Hughes K.T. Coupling of flagellar gene expression to flagellar assembly in Salmonella enterica serovar Typhimurium and Escherichia coli. Microbiol. Mol. Biol. Rev. 64:2000;694-708
44. Davey M.E., O'Toole G.A. Microbial biofilms: from ecology to molecular genetics. Microbiol. Mol. Biol. Rev. 64:2000;847-867
45. Josenhans C., Suerbaum S. The role of motility as a virulence factor in bacteria. Int. J. Med. Microbiol. 291:2002;605-614
46. Watnick P.I., Lauriano C.M., Klose K.E., Croal L., Kolter R. The absence of a flagellum leads to altered colony morphology, biofilm development and virulence in Vibrio cholerae O139. Mol. Microbiol. 39:2001;223-235
47. Ikeda J.S., et al. Flagellar phase variation of Salmonella enterica serovar Typhimurium contributes to virulence in the murine typhoid infection model but does not influence Salmonella-induced enteropathogenesis. Infect. Immun. 69:2001;3021-3030
48. Han Y.W., Uhl M.A., Han S.J., Shi W. Expression of bvgAS of Bordetella pertussis represses flagellar biosynthesis of Escherichia coli. Arch. Microbiol. 171:1999;127-130
49. Schmitt C.K., et al. Absence of all components of the flagellar export and synthesis machinery differentially alters virulence of Salmonella enterica serovar Typhimurium in models of typhoid fever, survival in macrophages, tissue culture invasiveness, and calf enterocolitis. Infect. Immun. 69:2001;5619-5625