Modulation of stress and virulence in Listeria monocytogenes

Trends in Microbiology

Volumn 16, Issue 8, 2008, Pages 388-396

  Chaturongakul, Soraya ^a   Raengpradub, Sarita ^b   Wiedmann, Martin ^c   Boor, Kathryn J ^c  

^a MAHIDOL UNIVERSITY   (Thailand)

^b Silliker Inc   (United States)

^c Cornell University ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RNA POLYMERASE; SIGMA FACTOR; VIRULENCE FACTOR;

BACILLUS SUBTILIS; BACTERIAL GENE; BACTERIAL METABOLISM; BACTERIAL VIRULENCE; ESCHERICHIA COLI; GENE CONTROL; HUMAN; LISTERIA MONOCYTOGENES; LISTERIOSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; STRESS;

BACTERIAL PROTEINS; GENE EXPRESSION REGULATION, BACTERIAL; LISTERIA MONOCYTOGENES; SIGMA FACTOR; VIRULENCE; VIRULENCE FACTORS;

BACTERIA (MICROORGANISMS); LISTERIA MONOCYTOGENES;

EID: 48149114272     PISSN: 0966842X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tim.2008.05.006     Document Type: Review

References (83)

1. r. Hyde. Infect. Immun. 74 (2006) 2505-2512
2. Lecuit M. Human listeriosis and animal models. Microbes Infect. 9 (2007) 1216-1225
3. Farber J.M., and Losos J.Z. Listeria monocytogenes: a foodborne pathogen. CMAJ 138 (1988) 413-418
4. Mead P.S., et al. Food-related illness and death in the United States. Emerg. Infect. Dis. 5 (1999) 607-625
5. Vazquez-Boland J.A., et al. Listeria pathogenesis and molecular virulence determinants. Clin. Micro. Rev. 14 (2001) 584-640
6. Jensen V.B., et al. Interactions of the invasive pathogens Salmonella Typhimurium, Listeria monocytogenes, and Shigella flexneri with M cells and murine Peyer's patches. Infect. Immun. 66 (1998) 3758-3766
7. Sauders B.D., and Wiedmann M. Ecology of Listeria species and L. monocytogenes in the natural environment. In: Ryser E.T., and Marth E.H. (Eds). Listeria, Listeriosis, and Food Safety. 3rd edn (2007), CRC Press 21-53
8. Wiedmann M., et al. Ribotype diversity of Listeria monocytogenes strains associated with outbreaks of listeriosis in ruminants. J. Clin. Microbiol. 34 (1996) 1086-1090
9. Gombas D.E., et al. Survey of Listeria monocytogenes in ready-to-eat foods. J. Food Prot. 66 (2003) 559-569
10. Rocourt J., and Buchrieser C. The genus Listeria and Listeria monocytogenes: phylogenetic position, taxonomy, and identification. In: Ryser E.T., and Marth E.H. (Eds). Listeria, Listeriosis, and Food Safety. 3rd edn (2007), CRC Press 1-20
11. B and its role in acid resistance and virulence of Listeria monocytogenes. J. Bacteriol. 180 (1998) 3650-3656
12. Begley M., et al. Bile stress response in Listeria monocytogenes LO28: adaptation, cross-protection, and identification of genetic loci involved in bile resistance. Appl. Environ. Microbiol. 8 (2002) 6005-6012
13. Karatzas K.A., and Bennik M.H. Characterization of a Listeria monocytogenes Scott A isolate with high tolerance towards high hydrostatic pressure. Appl. Environ. Microbiol. 68 (2002) 3183-3189
14. Conte M.P., et al. Effect of acid adaptation on the fate of Listeria monocytogenes in THP-1 human macrophages activated by γ interferon. Infect. Immun. 70 (2002) 4369-4378
15. B in survival of lethal acidic conditions and in the acquired acid tolerance response. Appl. Environ. Microbiol. 69 (2003) 2692-2698
16. Kazmierczak M.J., et al. Alternative σ factors and their roles in bacterial virulence. Micro. Mol. Biol. Rev. 69 (2005) 527-543
17. Magnusson L.U., et al. ppGpp: a global regulator in Escherichia coli. Trends Microbiol. 13 (2005) 236-242
18. E in Escherichia coli by both direct and indirect mechanisms. Mol. Microbiol. 67 (2008) 619-632
19. Stragier P., and Losick R. Molecular genetics of sporulation in Bacillus subtilis. Annu. Rev. Gen. 30 (1996) 297-341
20. Glaser P., et al. Comparative genomics of Listeria species. Science 294 (2001) 849-852
21. Xu J., et al. A genomic view of the human-Bacteroides thetaiotaomicron symbiosis. Science 299 (2003) 2074-2076
22. Kunst F., et al. The complete genome sequence of the gram-positive bacterium Bacillus subtilis. Nature 390 (1997) 249-256
23. B in the utilization of glycerol. Appl. Environ. Microbiol. 74 (2008) 594-604
24. B regulates stress response and virulence functions. J. Bacteriol. 185 (2003) 5722-5734
25. B-dependent stress responses in Listeria monocytogenes and Listeria innocua strains exposed to selected stress conditions. Appl. Environ. Microbiol. 74 (2008) 158-171
26. Hecker M., et al. SigB-dependent general stress response in Bacillus subtilis and related gram-positive bacteria. Annu. Rev. Microbiol. 61 (2007) 215-236
27. Petersohn A., et al. Global analysis of the general stress response of Bacillus subtilis. J. Bacteriol. 183 (2001) 5617-5631
28. B regulon. J. Bacteriol. 186 (2004) 4085-4099
29. B-controlled genes and their impact on acid stress, high hydrostatic pressure, and freeze survival in Listeria monocytogenes EGD-e. Appl. Environ. Microbiol. 70 (2004) 3457-3466
30. B-dependent survival under environmental, energy and intracellular stress conditions in Listeria monocytogenes. Appl. Environ. Microbiol. 70 (2004) 5349-5356
31. B and PrfA to expression of virulence and stress response genes during extra- and intracellular growth. Microbiology 152 (2006) 1827-1838
32. Cotter P.D., et al. Presence of GadD1 glutamate decarboxylase in selected Listeria monocytogenes strains is associated with an ability to grow at low pH. Appl. Environ. Microbiol. 71 (2005) 2832-2839
33. B from Listeria monocytogenes and its role in osmotolerance. J. Bacteriol. 180 (1998) 4547-4554
34. B-dependent expression patterns of compatible solute transporter genes opuCA and lmo1421 and a conjugated bile salt hydrolase bsh in Listeria monocytogenes. Microbiology 149 (2003) 3247-3256
35. B-dependent. Appl. Environ. Microbiol. 69 (2003) 2015-2022
36. B, in Listeria monocytogenes. J. Bacteriol. 186 (2004) 794-802
37. Moorhead S.M., and Dykes G.A. The role of the sigB gene in the general stress response of Listeria monocytogenes varies between a strain of serotype 1/2a and a strain of serotype 4c. Curr. Microbiol. 46 (2003) 461-466
38. B regulon. BMC Microbiol. 8 (2008) 20
39. B in heat, ethanol, acid, and oxidative stress resistance and during carbon starvation in Listeria monocytogenes. Appl. Environ. Microbiol. 67 (2001) 4454-4457
40. B activation under environmental and energy stress conditions in Listeria monocytogenes. Appl. Environ. Microbiol. 72 (2006) 5197-5203
41. Dussurget O., et al. 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
42. Sleator R.D., et al. A PrfA-regulated bile exclusion system (BilE) is a novel virulence factor in Listeria monocytogenes. Mol. Microbiol. 55 (2005) 1183-1195
43. B and the virulence gene regulator PrfA both regulate transcription of Listeria monocytogenes internalins. Appl. Environ. Microbiol. 73 (2007) 2919-2930
44. B contributes to PrfA-mediated virulence in Listeria monocytogenes. Infect. Immun. 70 (2002) 3948-3952
45. B in a growth phase dependent manner. FEMS Microbiol. Lett. 245 (2005) 329-336
46. Sleator R.D., et al. Analysis of the role of OpuC, an osmolyte transport system, in salt tolerance and virulence potential of Listeria monocytogenes. Appl. Environ. Microbiol. 67 (2001) 2692-2698
47. Chatterjee S.S., et al. Intracellular gene expression profile of Listeria monocytogenes. Infect. Immun. 74 (2006) 1323-1338
48. Joseph B., et al. Identification of Listeria monocytogenes genes contributing to intracellular replication by expression profiling and mutant screening. J. Bacteriol. 188 (2006) 556-568
49. B contributes to Listeria monocytogenes invasion by controlling expression of inlA and inlB. Microbiology 151 (2005) 3215-3222
50. B contributes to Listeria monocytogenes gastrointestinal infection but not to systemic spread in the guinea pig infection model. Infect. Immun. 74 (2006) 876-886
51. B factor from Bacillus anthracis and its role in virulence. J. Bacteriol. 182 (2000) 5036-5045
52. Britton R.A., et al. Genome-wide analysis of the stationary-phase sigma factor (Sigma-H) regulon of Bacillus subtilis. J. Bacteriol. 184 (2002) 4881-4890
53. Rea R.B., et al. Disruption of putative regulatory loci in Listeria monocytogenes demonstrates a significant role for Fur and PerR in virulence. Infect. Immun. 72 (2004) 717-727
54. Morikawa K., et al. A new staphylococcal σ factor in the conserved gene cassette: functional significance and implication for the evolutionary processes. Genes Cells 8 (2003) 699-712
55. H is required for toxin gene expression by Bacillus anthracis. J. Bacteriol. 189 (2007) 1874-1883
56. Robichon D., et al. The rpoN (σ-54) gene from Listeria monocytogenes is involved in resistance to mesentericin Y105, an antibacterial peptide from Leuconostoc mesenteroides. J. Bacteriol. 179 (1997) 7591-7594
57. Liu S., et al. Identification of Listeria monocytogenes genes expressed in response to growth at low temperature. Appl. Environ. Microbiol. 68 (2002) 1697-1705
58. Chan Y.C., et al. Microarray-based characterization of the Listeria monocytogenes cold regulon in log- and stationary-phase cells. Appl. Environ. Microbiol. 73 (2007) 6484-6498
59. 54-dependent PTS permease of the mannose family is responsible for sensitivity of Listeria monocytogenes to mesentericin Y105. Microbiology 147 (2001) 3263-3269
60. Arous S., et al. Global analysis of gene expression in an rpoN mutant of Listeria monocytogenes. Microbiology 150 (2004) 1581-1590
61. 54) is involved in osmotolerance in Listeria monocytogenes. FEMS Microbiol. Lett. 263 (2006) 54-60
62. E subunit of Escherichia coli RNA polymerase: a second alternative σ factor involved in high-temperature gene expression. Genes Dev. 3 (1989) 1462-1471
63. Wang Q.P., and Kaguni J.M. A novel sigma factor is involved in expression of the rpoH gene of Escherichia coli. J. Bacteriol. 171 (1989) 4248-4253
64. C and LstR, a lineage II-specific heat shock system. J. Bacteriol. 187 (2005) 7243-7253
65. Bennett H.J., et al. Characterization of relA and codY mutants of Listeria monocytogenes: identification of the CodY regulon and its role in virulence. Mol. Microbiol. 63 (2007) 1453-1467
66. B in Listeria monocytogenes. Appl. Environ. Microbiol. 73 (2007) 7967-7980
67. B in Listeria monocytogenes. Appl. Environ. Microbiol. 73 (2007) 7981-7991
68. Kirstein J., et al. A tyrosine kinase and its activator control the activity of the CtsR heat shock repressor in B. subtilis. EMBO J. 24 (2005) 3435-3445
69. Kruger E., et al. Clp-mediated proteolysis in gram-positive bacteria is autoregulated by the stability of repressor. EMBO J. 20 (2001) 852-863
70. Christiansen J.K., et al. The RNA-binding protein Hfq of Listeria monocytogenes: role in stress tolerance and virulence. J. Bacteriol. 186 (2004) 3355-3362
71. Gottesman S. The small RNA regulators of Escherichia coli: roles and mechanisms. Annu. Rev. Microbiol. 58 (2004) 303-328
72. McNealy T.L., et al. The Hfq homolog in Legionella pneumophila demonstrates regulation by LetA and RpoS and interacts with the global regulator CsrA. J. Bacteriol. 187 (2005) 1527-1532
73. Severino P., et al. Comparative transcriptome analysis of Listeria monocytogenes strains of the two major lineages reveals differences in virulence, cell wall, and stress response. Appl. Environ. Microbiol. 73 (2007) 6078-6088
74. B in adaptation of Listeria monocytogenes to growth at low temperature. J. Bacteriol. 182 (2000) 7083-7087
75. Moorhead S.M., and Dykes G.A. Influence of sigB gene on the cold stress survival and subsequent recovery of two Listeria monocytogenes serotypes. Int. J. Food Microbiol. 91 (2004) 63-72
76. B-independent mechanisms contribute to transcription of Listeria monocytogenes cold stress genes during cold shock and cold growth. Appl. Environ. Microbiol. 73 (2007) 6019-6029
77. B-dependent gene expression and induction in Listeria monocytogenes during osmotic and acid stress conditions simulating the intestinal environment. Microbiology 150 (2004) 3843-3855
78. Johansson J., et al. An RNA thermosensor controls expression of virulence genes in Listeria monocytogenes. Cell 110 (2002) 551-561
79. Freitag N.E., and Portnoy D.A. Dual promoters of the Listeria monocytogenes prfA transcriptional activator appear essential in vitro but are redundant in vivo. Mol. Microbiol. 12 (1994) 845-853
80. Bischoff M., et al. Influence of a functional sigB operon on the global regulators sar and agr in Staphylococcus aureus. J. Bacteriol. 183 (2001) 5171-5179
81. Arvidson S., and Tegmark K. Regulation of virulence determinants in Staphylococcus aureus. Int. J. Med. Microbiol. 291 (2001) 159-170
82. Milohanic E., et al. Transcriptome analysis of Listeria monocytogenes identifies three groups of genes differently regulated by PrfA. Mol. Microbiol. 47 (2003) 1613-1625
83. Mogk A., et al. The GroE chaperonin machine is a major modulator of the CIRCE heat shock regulon of Bacillus subtilis. EMBO J. 16 (1997) 4579-4590