Do Salmonella carry spare tyres?

Trends in Microbiology

Volumn 16, Issue 4, 2008, Pages 142-148

  McQuiston, John R ^a,b   Fields, Patricia I ^b   Tauxe, Robert V ^a,b   Logsdon Jr , John M ^a,c  

^a EMORY UNIVERSITY   (United States)

^b CENTERS FOR DISEASE CONTROL AND PREVENTION   (United States)

^c UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLAGELLIN;

ARTICLE; BACTERIAL FLAGELLUM; BACTERIAL GENOME; ECOLOGICAL NICHE; ENVIRONMENTAL FACTOR; GENE EXPRESSION; GENE LOCUS; GENETIC CODE; MOLECULAR EVOLUTION; NONHUMAN; PHYLOGENY; PREDATION; PRIORITY JOURNAL; PROTOZOON; SALMONELLA; SALMONELLA BONGORI; SALMONELLA ENTERICA; SEROTYPE; SPECIES DIFFERENCE; SUBSPECIES;

ANIMALS; EVOLUTION; FLAGELLIN; GENE EXPRESSION REGULATION, BACTERIAL; HUMANS; MODELS, GENETIC; PREDATORY BEHAVIOR; PROTOZOA; SALMONELLA; SALMONELLA ENTERICA; SEROTYPING; VARIATION (GENETICS);

ENTEROBACTERIACEAE; SALMONELLA;

EID: 41549089094     PISSN: 0966842X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tim.2008.01.009     Document Type: Article

References (59)

1. Voetsch A.C., et al. FoodNet estimate of the burden of illness caused by nontyphoidal Salmonella infections in the United States. Clin. Infect. Dis. 38 Suppl 3 (2004) S127-S134
2. Salmonella Subcommittee of the International Society of Microbiology. The genus Salmonella lignieres, 1900. Journal of Hygiene 22 (1934) 333-350
3. Kauffmann F. The Bacteriology of Enterobacteriaceae (1966), The Williams and Wilkins Company pp.56-104
4. Popoff M.Y., et al. Supplement 2002 (no. 46) to the Kauffmann-White scheme. Res. Microbiol. 155 (2004) 568-570
5. Hueck C.J. Type III protein secretion systems in bacterial pathogens of animals and plants. Microbiol. Mol. Biol. Rev. 62 (1998) 379-433
6. McNab R.M. Flagella and motility. In: Neidhardt F.C. (Ed). Escherichia coli and Salmonella. 2nd edn (1996), ASM Press 123-145
7. Silverman M., and Simon M. Phase variation: genetic analysis of switching mutants. Cell 19 (1980) 845-854
8. Belas R., and Flaherty D. Sequence and genetic analysis of multiple flagellin-encoding genes from Proteus mirabilis. Gene 148 (1994) 33-41
9. Belas R. Expression of multiple flagellin-encoding genes of Proteus mirabilis. J. Bacteriol. 176 (1994) 7169-7181
10. Guerry P., et al. Role of two flagellin genes in Campylobacter motility. J. Bacteriol. 173 (1991) 4757-4764
11. Guerry P., et al. Genomic rearrangements associated with antigenic variation in Campylobacter coli. J. Bacteriol. 170 (1988) 316-319
12. Ren C.P., et al. The Flag-2 locus, an ancestral gene cluster, is potentially associated with a novel flagellar system from Escherichia coli. J. Bacteriol. 187 (2005) 1430-1440
13. Zieg J., et al. Regulation of gene expression by site-specific inversion. Cell 15 (1978) 237-244
14. Zieg J., et al. Recombinational switch for gene expression. Science 196 (1977) 170-172
15. Zieg J., and Simon M. Analysis of the nucleotide sequence of an invertible controlling element. Proc. Natl. Acad. Sci. U. S. A. 77 (1980) 4196-4200
16. 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
17. Groisman E.A., and Ochman H. How Salmonella became a pathogen. Trends Microbiol. 5 (1997) 343-349
18. Torpdahl M., and Ahrens P. Population structure of Salmonella investigated by amplified fragment length polymorphism. J. Appl. Microbiol. 97 (2004) 566-573
19. Porwollik S., et al. Evolutionary genomics of Salmonella: gene acquisitions revealed by microarray analysis. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 8956-8961
20. Ochman H., and Groisman E.A. Distribution of pathogenicity islands in Salmonella spp. Infect. Immun. 64 (1996) 5410-5412
21. Scott F., et al. Genetic structure of Salmonella revealed by fragment analysis. Int. J. Syst. Evol. Microbiol. 52 (2002) 1701-1713
22. Boyd E.F., et al. Molecular genetic relationships of the salmonellae. Appl. Environ. Microbiol. 62 (1996) 804-808
23. Chan K., et al. 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
24. Baumler A.J. The record of horizontal gene transfer in Salmonella. Trends Microbiol. 5 (1997) 318-322
25. Herikstad H., et al. Salmonella surveillance: a global survey of public health serotyping. Epidemiol. Infect. 129 (2002) 1-8
26. McQuiston J.R., et al. Sequencing and comparative analysis of flagellin genes fliC, fljB, and flpA from Salmonella. J. Clin. Microbiol. 42 (2004) 1923-1932
27. Chadfield M.S., et al. Comparison of intestinal invasion and macrophage response of Salmonella Gallinarum and other host-adapted Salmonella enterica serovars in the avian host. Vet. Microbiol. 92 (2003) 49-64
28. Li J., et al. Evolutionary origin and radiation of the avian-adapted non-motile salmonellae. J. Med. Microbiol. 38 (1993) 129-139
29. Baker S., et al. A novel linear plasmid mediates flagellar variation in Salmonella Typhi. PLoS Pathog 3 (2007) e59. http://www.plospathogens.org 10.1371/journal.ppat.0030059
30. Frankel G. Intragenic recombination in a flagellin gene: characterization of the H1-j gene of Salmonella typhi. EMBO J. 8 (1989) 3149-3152
31. Macnab R.M., and DeRosier D.J. Bacterial flagellar structure and function. Can. J. Microbiol. 34 (1988) 442-451
32. Tominaga A., et al. Molecular characterization of intact, but cryptic, flagellin genes in the genus Shigella. Mol. Microbiol. 12 (1994) 277-285
33. Prouty A.M., et al. Biofilm formation and interaction with the surfaces of gallstones by Salmonella spp. Infect. Immun. 70 (2002) 2640-2649
34. Burkart M., et al. The chemotaxis system, but not chemotaxis, is essential for swarming motility in Escherichia coli. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 2568-2573
35. Hughes K.T., et al. Sensing structural intermediates in bacterial flagellar assembly by export of a negative regulator. Science 262 (1993) 1277-1280
36. Wang Q., et al. Sensing wetness: a new role for the bacterial flagellum. EMBO J. 24 (2005) 2034-2042
37. Barbour A.G., and Restrepo B.I. Antigenic variation in vector-borne pathogens. Emerg. Infect. Dis. 6 (2000) 449-457
38. Inzana T.J., et al. Phase variation and conservation of lipooligosaccharide epitopes in Haemophilus somnus. Infect. Immun. 65 (1997) 4675-4681
39. Finlay B.B., and McFadden G. Anti-immunology: evasion of the host immune system by bacterial and viral pathogens. Cell 124 (2006) 767-782
40. Deitsch K.W., et al. Shared themes of antigenic variation and virulence in bacterial, protozoal, and fungal infections. Microbiol. Mol. Biol. Rev. 61 (1997) 281-293
41. Hayashi F., and Auvray F. The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5 Flagellin polymerisation control by a cytosolic export chaperone. Nature 410 (2001) 1099-1103
42. Sbrogio-Almeida M.E., et al. Host and bacterial factors affecting induction of immune responses to flagellin expressed by attenuated Salmonella vaccine strains. Infect. Immun. 72 (2004) 2546-2555
43. Stocker B.A., and Newton S.M. Immune responses to epitopes inserted in Salmonella flagellin. Int. Rev. Immunol. 11 (1994) 167-178
44. Didierlaurent A., et al. Flagellin promotes myeloid differentiation factor 88-dependent development of Th2-type response. J. Immunol. 172 (2004) 6922-6930
45. Means T.K., et al. The Toll-like receptor 5 stimulus bacterial flagellin induces maturation and chemokine production in human dendritic cells. J. Immunol. 170 (2003) 5165-5175
46. McDermott P.F., et al. High-affinity interaction between gram-negative flagellin and a cell surface polypeptide results in human monocyte activation. Infect. Immun. 68 (2000) 5525-5529
47. Fierer J., and Guiney D.G. Diverse virulence traits underlying different clinical outcomes of Salmonella infection. J. Clin. Invest. 107 (2001) 775-780
48. Li J., et al. Recombinational basis of serovar diversity in Salmonella enterica. Proc. Natl. Acad. Sci. U. S. A. 91 (1994) 2552-2556
49. Stocker B.A.D. Measurments of rate of mutation of flagellar antigenic phase in Salmonella Typhi-murium. J. Hyg. (Lond.) 47 (1949) 398-413
50. Wildschutte H., et al. Protozoan predation, diversifying selection, and the evolution of antigenic diversity in Salmonella. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 10644-10649
51. Matz C., and Jurgens K. High motility reduces grazing mortality of planktonic bacteria. Appl. Environ. Microbiol. 71 (2005) 921-929
52. Harb O.S., et al. From protozoa to mammalian cells: a new paradigm in the life cycle of intracellular bacterial pathogens. Environ. Microbiol. 2 (2000) 251-265
53. Old D.C. Nomenclature of Salmonella. J. Med. Microbiol. 37 (1992) 361-363
54. CDC (2005) Salmonella Surveillance: Annual Summary (2004) US Department of Health and Human Services
55. Garaizar J., et al. DNA microarray-based typing of an atypical monophasic Salmonella enterica serovar. J. Clin. Microbiol. 40 (2002) 2074-2078
56. McClelland M., et al. Complete genome sequence of Salmonella enterica serovar Typhimurium LT2. Nature 413 (2001) 852-856
57. Bonifield H.R., and Hughes K.T. Flagellar phase variation in Salmonella enterica is mediated by a posttranscriptional control mechanism. J. Bacteriol. 185 (2003) 3567-3574
58. Simon M., et al. Phase variation: evolution of a controlling element. Science 209 (1980) 1370-1374
59. Lederberg J., and Iino T. Phase variation in Salmonella. Genetics 41 (1956) 743-757