Central metabolism controls transcription of a virulence gene regulator in Vibrio cholerae

Microbiology (United Kingdom)

Volumn 159, Issue 4, 2013, Pages 792-802

  Minato, Yusuke ^a   Fassio, Sara R ^a   Wolfe, Alan J ^b   Häse, Claudia C ^a  

^a OREGON STATE UNIVERSITY   (United States)

^b LOYOLA UNIVERSITY CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; ACETYL COENZYME A; AMINO ACID; BACTERIAL PROTEIN; CITRIC ACID; OXALOACETIC ACID; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); TOLC PROTEIN; TOXT PROTEIN; TRICARBOXYLIC ACID; UNCLASSIFIED DRUG; VIRULENCE FACTOR;

ARTICLE; BACTERIAL GENE; BACTERIAL GROWTH; BACTERIAL METABOLISM; BACTERIAL VIRULENCE; BACTERIUM MUTANT; CITRIC ACID CYCLE; CONTROLLED STUDY; ENZYME INHIBITION; EXCRETION; MICROBIAL RESPIRATION; NONHUMAN; PH; PRIORITY JOURNAL; REGULATOR GENE; TRANSCRIPTION REGULATION; TRANSPOSON; VIBRIO CHOLERAE;

ACETATES; ACETYL COENZYME A; AMINO ACIDS; BACTERIAL PROTEINS; CITRIC ACID; CITRIC ACID CYCLE; CULTURE MEDIA; DNA TRANSPOSABLE ELEMENTS; GENE EXPRESSION REGULATION, BACTERIAL; MUTAGENESIS, INSERTIONAL; OXYGEN CONSUMPTION; TRANSCRIPTION FACTORS; VIBRIO CHOLERAE O1; VIRULENCE;

VIBRIO CHOLERAE;

EID: 84875708829     PISSN: 13500872     EISSN: 14652080     Source Type: Journal    
DOI: 10.1099/mic.0.064865-0     Document Type: Article

References (51)

1. +--translocating NADH:quinone oxidoreductase from Vibrio cholerae. Biochemistry 41, 3781-3789.
2. Brown, T. D., Jones-Mortimer, M. C. & Kornberg, H. L. (1977). The enzymic interconversion of acetate and acetyl-coenzyme A in Escherichia coli. J Gen Microbiol 102, 327-336.
3. Cherepanov, P. P. & Wackernagel, W. (1995). Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flpcatalyzed excision of the antibiotic-resistance determinant. Gene 158, 9-14.
4. Chubiz, L. M. & Rao, C. V. (2010). Aromatic acid metabolites of Escherichia coli K-12 can induce the marRAB operon. J Bacteriol 192, 4786-4789.
5. Datsenko, K. A. & Wanner, B. L. (2000). One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci U S A 97, 6640-6645.
6. Davies, B. W., Bogard, R. W., Young, T. S. & Mekalanos, J. J. (2012). Coordinated regulation of accessory genetic elements produces cyclic di-nucleotides for V. cholerae virulence. Cell 149, 358-370.
7. Dehio, C. & Meyer, M. (1997). Maintenance of broad-host-range incompatibility group P and group Q plasmids and transposition of Tn5 in Bartonella henselae following conjugal plasmid transfer from Escherichia coli. J Bacteriol 179, 538-540.
8. Delbaere, L. T. J., Sudom, A. M., Prasad, L., Leduc, Y. & Goldie, H. (2004). Structure/function studies of phosphoryl transfer by phosphoenolpyruvate carboxykinase. Biochim Biophys Acta 1697, 271-278.
9. Deutscher, J. (2008). The mechanisms of carbon catabolite repression in bacteria. Curr Opin Microbiol 11, 87-93.
10. Dhamdhere, G. & Zgurskaya, H. I. (2010). Metabolic shutdown in Escherichia coli cells lacking the outer membrane channel TolC. Mol Microbiol 77, 743-754.
11. DiRita, V. J., Parsot, C., Jander, G. & Mekalanos, J. J. (1991). Regulatory cascade controls virulence in Vibrio cholerae. Proc Natl Acad Sci U S A 88, 5403-5407.
12. Donnenberg, M. S. & Kaper, J. B. (1991). Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector. Infect Immun 59, 4310-4317.
13. Gardel, C. L. & Mekalanos, J. J. (1994). Regulation of cholera toxin by temperature, pH, and osmolarity. Methods Enzymol 235, 517-526.
14. Gardel, C. L. & Mekalanos, J. J. (1996). Alterations in Vibrio cholerae motility phenotypes correlate with changes in virulence factor expression. Infect Immun 64, 2246-2255.
15. Görke, B. & Stülke, J. (2008). Carbon catabolite repression in bacteria: many ways to make the most out of nutrients. Nat Rev Microbiol 6, 613-624.
16. Guccione, E., del Rocio Leon-Kempis, M, Pearson, B. M., Hitchin, E., Mulholland, F., van Diemen, P. M., Stevens, M. P.& Kelly, D. J. (2008). Amino acid-dependent growth of Campylobacter jejuni: key roles for aspartase (AspA) under microaerobic and oxygen-limited conditions and identification of AspB (Cj0762), essential for growth on glutamate. Mol Microbiol 69, 77-93.
17. Häse, C. C. (2001). Analysis of the role of flagellar activity in virulence gene expression in Vibrio cholerae. Microbiology 147, 831-837.
18. Häse, C. C. & Mekalanos, J. J. (1998). TcpP protein is a positive regulator of virulence gene expression in Vibrio cholerae. Proc Natl Acad Sci U S A 95, 730-734.
19. Häse, C. C. & Mekalanos, J. J. (1999). Effects of changes in membrane sodium flux on virulence gene expression in Vibrio cholerae. Proc Natl Acad Sci U S A 96, 3183-3187.
20. Hu, L. I., Lima, B. P. & Wolfe, A. J. (2010). Bacterial protein acetylation: the dawning of a new age. Mol Microbiol 77, 15-21.
21. Inada, T., Kimata, K. & Aiba, H. (1996). Mechanism responsible for glucose-lactose diauxie in Escherichia coli: challenge to the cAMP model. Genes Cells 1, 293-301.
22. Koronakis, V., Eswaran, J. & Hughes, C. (2004). Structure and function of TolC: the bacterial exit duct for proteins and drugs. Annu Rev Biochem 73, 467-489.
23. Kovacikova, G. & Skorupski, K. (2001). Overlapping binding sites for the virulence gene regulators AphA, AphB and cAMP-CRP at the Vibrio cholerae tcpPH promoter. Mol Microbiol 41, 393-407.
24. Kovacikova, G., Lin, W. & Skorupski, K. (2010). The LysR-type virulence activator AphB regulates the expression of genes in Vibrio cholerae in response to low pH and anaerobiosis. J Bacteriol 192, 4181-4191.
25. Lakshmi, T. M. & Helling, R. B. (1976). Selection for citrate synthase deficiency in icd mutants of Escherichia coli. J Bacteriol 127, 76-83.
26. Leigh, J. A. & Dodsworth, J. A. (2007). Nitrogen regulation in bacteria and archaea. Annu Rev Microbiol 61, 349-377.
27. Lima, B. P., Antelmann, H., Gronau, K., Chi, B. K., Becher, D., Brinsmade, S. R. & Wolfe, A. J. (2011). Involvement of protein acetylation in glucose-induced transcription of a stress-responsive promoter. Mol Microbiol 81, 1190-1204.
28. Lima, B. P., Thanh Huyen, T. T., Bäsell, K., Becher, D., Antelmann, H. & Wolfe, A. J. (2012). Inhibition of acetyl phosphate-dependent transcription by an acetylatable lysine on RNA polymerase. J Biol Chem 287, 32147-32160.
29. Mascher, T., Helmann, J. D. & Unden, G. (2006). Stimulus perception in bacterial signal-transducing histidine kinases. Microbiol Mol Biol Rev 70, 910-938.
30. Matson, J. S., Withey, J. H. & DiRita, V. J. (2007). Regulatory networks controlling Vibrio cholerae virulence gene expression. Infect Immun 75, 5542-5549.
31. Metcalf, W. W., Jiang, W., Daniels, L. L., Kim, S. K., Haldimann, A. & Wanner, B. L. (1996). Conditionally replicative and conjugative plasmids carrying lacZa for cloning, mutagenesis, and allele replacement in bacteria. Plasmid 35, 1-13.
32. Miller, V. L. & Mekalanos, J. J. (1988). A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR. J Bacteriol 170, 2575-2583.
33. Minato, Y., Siefken, R. L. & Häse, C. C. (2011). TolC affects virulence gene expression in Vibrio cholerae. J Bacteriol 193, 5850-5852.
34. Nye, M. B., Pfau, J. D., Skorupski, K. & Taylor, R. K. (2000). Vibrio cholerae H-NS silences virulence gene expression at multiple steps in the ToxR regulatory cascade. J Bacteriol 182, 4295-4303.
35. Patra, T., Koley, H., Ramamurthy, T., Ghose, A. C. & Nandy, R. K. (2012). The Entner-Doudoroff pathway is obligatory for gluconate utilization and contributes to the pathogenicity of Vibrio cholerae. J Bacteriol 194, 3377-3385.
36. Postle, K. & Vakharia, H. (2000). TolC, a macromolecular periplasmic 'chunnel'. Nat Struct Biol 7, 527-530.
37. Reid, C. J. & Poole, P. S. (1998). Roles of DctA and DctB in signal detection by the dicarboxylic acid transport system of Rhizobium leguminosarum. J Bacteriol 180, 2660-2669.
38. Rose, I. A., Grunberg-Manago, M., Korey, S. R. & Ochoa, S. (1954). Enzymatic phosphorylation of acetate. J Biol Chem 211, 737-756.
39. Rosner, J. L. & Martin, R. G. (2009). An excretory function for the Escherichia coli outer membrane pore TolC: upregulation of marA and soxS transcription and Rob activity due to metabolites accumulated in tolC mutants. J Bacteriol 191, 5283-5292.
40. Rubin, E. J., Akerley, B. J., Novik, V. N., Lampe, D. J., Husson, R. N. & Mekalanos, J. J. (1999). In vivo transposition of mariner-based elements in enteric bacteria and mycobacteria. Proc Natl Acad Sci USA96, 1645-1650.
41. Santos, M. R., Cosme, A. M., Becker, J. D., Medeiros, J. M., Mata, M. F. & Moreira, L. M. (2010). Absence of functional TolC protein causes increased stress response gene expression in Sinorhizobium meliloti. BMC Microbiol 10, 180.
42. Scheu, P. D., Witan, J., Rauschmeier, M., Graf, S., Liao, Y. F., Ebert-Jung, A., Basché, T., Erker, W. & Unden, G. (2012). CitA/CitB two-component system regulating citrate fermentation in Escherichia coli and its relation to the DcuS/DcuR system in vivo. J Bacteriol 194, 636-645.
43. Skorupski, K. & Taylor, R. K. (1997). Control of the ToxR virulence regulon in Vibrio cholerae by environmental stimuli. Mol Microbiol 25, 1003-1009.
44. Stonehouse, E. A., Hulbert, R. R., Nye, M. B., Skorupski, K. & Taylor, R. K. (2011). H-NS binding and repression of the ctx promoter in Vibrio cholerae. J Bacteriol 193, 979-988.
45. Thao, S. & Escalante-Semerena, J. C. (2011). Control of protein function by reversible Nelysine acetylation in bacteria. Curr Opin Microbiol 14, 200-204.
46. Wolfe, A. J. (2005). The acetate switch. Microbiol Mol Biol Rev 69, 12- 50.
47. Wolfe, A. J. (2010). Physiologically relevant small phosphodonors link metabolism to signal transduction. Curr Opin Microbiol 13, 204- 209.
48. Yamamoto, S., Izumiya, H., Morita, M., Arakawa, E. & Watanabe. Application of λ; Red recombination system to Vibrio cholerae genetics: simple methods for inactivation and modification of chromosomal genes. Gene 438, 57-64.
49. Yu, B. J., Sung, B. H., Lee, J. Y., Son, S. H., Kim, M. S. & Kim, S. C. (2006). sucAB and sucCD are mutually essential genes in Escherichia coli. FEMS Microbiol Lett 254, 245-250.
50. Zgurskaya, H. I., Krishnamoorthy, G., Ntreh, A. & Lu, S. (2011). Mechanism and function of the outer membrane channel TolC in multidrug resistance and physiology of enterobacteria. Front Microbiol 2, 189.
51. Zientz, E., Bongaerts, J. & Unden, G. (1998). Fumarate regulation of gene expression in Escherichia coli by the DcuSR (dcuSR genes) twocomponent regulatory system. J Bacteriol 180, 5421-5425.