KatA, the major catalase, is critical for osmoprotection and virulence in Pseudomonas aeruginosa PA14

Infection and Immunity

Volumn 73, Issue 7, 2005, Pages 4399-4403

  Lee, Ji Sun ^a   Heo, Yun Jeong ^a   Lee, Jeong K ^a   Cho, You Hee ^a  

^a Sogang University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL PROTEIN; CATALASE; HYDROGEN PEROXIDE; PROTEIN KATA; PROTEIN KATB; PROTEIN KATE; UNCLASSIFIED DRUG;

ADAPTATION; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BACTERIAL STRAIN; BACTERIAL VIRULENCE; CONTROLLED STUDY; DROSOPHILA MELANOGASTER; MOUSE; NONHUMAN; OSMOTIC STRESS; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN FUNCTION; PSEUDOMONAS AERUGINOSA; PSEUDOMONAS AERUGINOSA PA14;

ANIMALS; CATALASE; DROSOPHILA MELANOGASTER; HYDROGEN PEROXIDE; POTASSIUM CHLORIDE; PSEUDOMONAS AERUGINOSA; VIRULENCE;

EID: 21544440596     PISSN: 00199567     EISSN: None     Source Type: Journal    
DOI: 10.1128/IAI.73.7.4399-4403.2005     Document Type: Article

References (28)

1. Bodey, G. P., R. Bolivar, V. Fainstein, and L. Jadeja. 1983. Infections caused by Pseudomonas aeruginosa. Rev. Infect. Dis. 5:279-313.
2. Brown, S. M., M. L. Howell, M. L. Vasil, A. J. Anderson, and D. J. Hassett. 1995. Cloning and characterization of the katB gene of Pseudomonas aeruginosa encoding a hydrogen peroxide-inducible catalase: purification of KatB, cellular localization, and demonstration that it is essential for optimal resistance to hydrogen peroxide. J. Bacteriol. 177:6536-6544.
3. Cho, Y.-H. 1999. Gene expression and the role of catalases in Streptomyces coelicolor A3(2). Ph.D. thesis. Seoul National University, Seoul, Korea.
4. Cho, Y.-H., and J.-H. Roe. 1997. Isolation and expression of the catA gene encoding the major vegetative catalase in Streptomyces coelicolor Müller. J. Bacteriol. 179:4049-4052.
5. Cho, Y.-H., E.-J. Lee, and J.-H. Roe. 2000. A developmentally regulated catalase required for proper differentiation and osmoprotection of Streptomyce coelicolor. Mol. Microbiol. 35:150-160.
6. Cho, Y.-H., E.-J. Lee, B.-E. Ahn, and J.-H. Roe. 2001. SigB, an RNA polymerase sigma factor required for osmoprotection and proper differentiation of Streptomyces coelicolor. Mol. Microbiol. 42:205-214.
7. Christman, M. F., R. W. Morgan, F. S. Jacobson, and B. N. Ames. 1985. Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimurium. Cell 41:753-762.
8. Demple, B., J. Halbrook, and S. Linn. 1983. Escherichia coli xth mutants are hypersensitive to hydrogen peroxide. J. Bacteriol. 153:1079-1082.
9. Dowds, B. C., P. Murphy, D. J. McConnell, and K. M. Devine. 1987. Relationship a mong oxidative stress, growth cycle, and sporulation in Bacillus subtilis. J. Bacteriol. 169:5771-5775.
10. Hassett, D. J., E. Alsabbagh, K. Parvatiyar, M. L. Howell, R. W. Wilmott, and U. A. Ochsner. 2000. A protease-resistant catalase, KatA, released upon cell lysis during stationary phase is essential for aerobic survival of a Pseudomonas aeruginosa oxyR mutant at low cell densities. J. Bacteriol. 182:4557-4563.
11. Hassett, D. J., J. F. Ma, J. G. Elkins, T. R. McDermott, U. A. Ochsner, S. E. West, C. T. Huang, J. Fredericks, S. Burnett, P. S. Stewart, G. McFeters, L. Passador, and B. H. Iglewski. 1999. Quorum sensing in Pseudomonas aeruginosa controls expression of catalase and superoxide dismutase genes and mediates biofilm susceptibility to hydrogen peroxide. Mol. Microbiol. 34: 1082-1093.
12. Igarashi, T., Y. Kono, and K. Tanaka. 1996. Molecular cloning of manganese catalase from Lactobacillus plantarum. J. Biol. Chem. 271:29521-29524.
13. Klotz, M. G., and P. C. Loewen. 2003. The molecular evolution of catalytic hydroperoxidases: evidence for multiple lateral transfer of genes between prokaryota and from bacteria into eukaryota. Mol. Biol. Evol. 20:1098-1112.
14. Klotz, M. G., G. R. Klassen, and P. C. Loewen. 1997. Phylogenetic relationships among prokaryotic and eukaryotic catalases. Mol. Biol. Evol. 14:951-958.
15. Lee, J.-S. 2005. Phenotypic analyses of of monofunctional catalases in Pseudomonas aeruginosa. M.S. thesis. Sogang University, Seoul, Korea.
16. Lee, J.-S., S.-H. Kim, and Y.-H. Cho. 2004. Dithiothreitol attenuates the pathogenic interaction between Pseudomonas aeruginosa and Drosophila melanogaster. J. Microbiol. Biotechnol. 14:367-372.
17. Lee, J.-S., Y.-C. Hah, and J.-H. Roe. 1993. The induction of oxidative enzymes in Streptomyces coelicolor upon hydrogen peroxide treatment. J. Gen. Microbiol. 139:1013-1018.
18. Ochsner, U. A., M. L. Vasil, E. Alsabbagh, K. Parvatiyar, and D. J. Hassett. 2000. Role of the Pseudomonas aeruginosa oxyR-recG operon in oxidative stress defense and DNA repair: OxyR-dependent regulation of katB-ankB, ahpB, and ahpC-ahpF. J. Bacteriol. 182:4533-4544.
19. Palma, M., D. DeLuca, S. Worgall, and L. E. Quadri. 2004. Transcriptome analysis of the response of Pseudomonas aeruginosa to hydrogen peroxide. J. Bacteriol. 186:248-252.
20. Rahme, L. G., E. J. Stevens, S. F. Wolfort, J. Shao, R. G. Tompkins, and F. M. Ausubel. 1995. Common virulence factors for bacterial pathogenicity in plants and animals. Science 268:1899-1902.
21. S). Mol. Microbiol. 39:1533-1545.
22. Schweizer, H. P. 1991. Escherichia-Pseudomonas shuttle vectors derived from pUC18/19. Gene 97:109-121.
23. Shortridge, V. D., A. Lazdunski, and M. L. Vasil. 1992. Osmoprotectants and phosphate regulate expression of phospholipase C in Pseudomonas aeruginosa. Mol. Microbiol. 6:863-871.
24. Sonnleitner, E., S. Hagens, F. Rosenau, S. Wilhelm, A. Habel, K. E. Jager, and U. Blasi. 2003. Reduced virulence of a hfq mutant of Pseudomonas aeruginosa O1. Microb. Pathog. 35:217-228.
25. Stover, C. K., X. Q. Pham, A. L. Erwin, S. D. Mizoguchi, P. Warrener, M. J. Hickey, F. S. Brinkman, W. O. Hufnagle, D. J. Kowalik, M. Lagrou, R. L. Garber, L. Goltry, E. Tolentino, S. Westbrock-Wadman, Y. Yuan, L. L. Brody, S. N. Coulter, K. R. Folger, A. Kas, K. Larbig, R. Lim, K. Smith, D. Spencer, G. K. Wong, Z. Wu, I. T. Paulsen, J. Reizer, M. H. Saier, R. E. Hancock, S. Lory, and M. V. Olson. 2000. Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen. Nature 406:959-964.
26. Suh, S. J., L. Silo-Sun, D. E. Woods, D. J. Hassett, S. E. West, and D. E. Ohman. 1999. Effect of rpoS mutation on the stress response and expression of virulence factors in Pseudomonas aeruginosa. J. Bacteriol. 181:3890-3897.
27. Vodovar, N., C. Acosta, B. Lemaitre, and F. Boccard. 2004. Drosophila: a polyvalent model to decipher host-pathogen interactions. Trends Microbiol. 12:235-242.
28. Wolfgang, M. C., B. R. Kulasekara, X. Liang, D. Boyd, K. Wu, Q. Yang, C. G. Miyada, and S. Lory. 2003. Conservation of genome content and virulence determinants among clinical and environmental isolates of Pseudomonas aeruginosa. Proc. Natl. Acad. Sci. USA 100:8484-8489.