Comparative analysis of extracellular enzymes and virulence exhibited by Burkholderia pseudomallei from different sources

Microbial Pathogenesis

Volumn 47, Issue 3, 2009, Pages 111-117

  Vellasamy, Kumutha Malar ^a   Vasu, Chenthamarakshan ^a   Puthucheary, Savithri Devi ^a   Vadivelu, Jamuna ^a  

^a UNIVERSITY OF MALAYA   (Malaysia)

Author keywords

Burkholderia pseudomallei; Culture filtrate; Extracellular enzymes; Virulence

Indexed keywords

BACTERIAL ENZYME; CATALASE; PEROXIDASE; PHOSPHOLIPASE C; PROTEINASE; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BACTEREMIA; BACTERIAL GROWTH; BACTERIAL STRAIN; BACTERIAL VIRULENCE; BACTERIUM CULTURE; BACTERIUM ISOLATE; BURKHOLDERIA PSEUDOMALLEI; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME SYNTHESIS; FEMALE; IN VITRO STUDY; IN VIVO STUDY; MELIOIDOSIS; MORTALITY; MOUSE; NONHUMAN; PRIORITY JOURNAL; SPLEEN ABSCESS;

ANIMALS; BACTERIAL PROTEINS; BURKHOLDERIA INFECTIONS; BURKHOLDERIA PSEUDOMALLEI; CATALASE; FEMALE; MICE; MICE, INBRED ICR; PEROXIDASE; PHOSPHORIC MONOESTER HYDROLASES; SOIL MICROBIOLOGY; VIRULENCE;

BURKHOLDERIA PSEUDOMALLEI; MUS;

EID: 68149179655     PISSN: 08824010     EISSN: 10961208     Source Type: Journal    
DOI: 10.1016/j.micpath.2009.06.003     Document Type: Article

References (53)

1. Leelarasamee A. Recent development in melioidosis. Curr Opin Infect Dis 17 (2004) 131-136
2. Stevens M.P., Haque A., Atkins T., Hill J., Wood M.W., Easton A., et al. Attenuated virulence and protective efficacy of a Burkholderia pseudomallei bsa type III secretion mutant in murine models of melioidosis. Microbiol 150 (2004) 2669-2676
3. Puthucheary S.D., and Vadivelu J. Human melioidosis. 1st ed. (2002), Singapore University Press, Republic of Singapore
4. White N.J. Melioidosis. Lancet 361 (2003) 1715-1722
5. Ashdown L.R., and Koehler J.M. Production of hemolysin and other extracellular enzymes by clinical isolates of Pseudomonas pseudomallei. J Clin Microbiol 28 (1990) 2331-2334
6. Yang H., Chaowagul W., and Sokol P.A. Siderophore production by Pseudomonas pseudomallei. Infect Immun 59 (1991) 776-780
7. Steven J., Pietro R., Marianela E., Andrew O., Janet E.D., Susan B., et al. Self-chaperoning of the type III secretion system needle tip proteins IpaD and BipD. J Biol Chem 282 (2007) 4035-4044
8. Holden M.T.G., Titball R.W., Peacock S.J., Cerdeno-Tarraga A.M., Atkins T., Crossman L.C., et al. Genomic plasticity of the causative agent of melioidosis, Burkholderia pseudomallei. Proc Natl Acad Sci U S A 101 (2004) 14240-14245
9. Chua K.L., Chan Y.Y., and Gan Y.H. Flagella are virulence determinants of Burkholderia pseudomallei. Infect Immun 71 (2003) 1622-1629
10. Stevens M.P., Wood M.W., Taylor L.A., Monaghan P., Hawes P., Jones P.W., et al. An Inv/Mxi-Spa-like type III protein secretion system in Burkholderia pseudomallei modulates intracellular behaviour of the pathogen. Mol Microbiol 46 (2002) 649-659
11. Reckseidler S.L., DeShazer D., Sokol P.A., and Woods D.E. Detection of bacterial virulence genes by subtractive hybridization: identification of capsular polysaccharide of Burkholderia pseudomallei as a major virulence determinant. Infect Immun 69 (2001) 34-44
12. Kespichayawattana W., Intachote P., Utaisincharoen P., and Sirisinha S. Virulent Burkholderia pseudomallei is more efficient than avirulent Burkholderia thailandensis in invasion of and adherence to cultured human epithelial cells. Microb Pathog 36 (2004) 287-292
13. Jones A.L., Beveridge T.J., and Woods D.E. Intracellular survival of Burkholderia pseudomallei. Infect Immun 64 (1996) 782-790
14. Pruksachartvuthi S., Aswapokee N., and Thankerngpol K. Survival of Pseudomonas pseudomallei in human phagocytes. J Med Microbiol 31 (1990) 109-114
15. Sexton M.M., Jones A.L., Chaowagul W., and Woods D.E. Purification and characterization of a protease from Pseudomonas pseudomallei. Can J Microbiol 40 (1994) 903-910
16. Ostanin K., Harms E.H., Stevis P.E., Kuciel R., Zhou M.M., and Van Etten R.L. Overexpression, site-directed mutagenesis and mechanism of Escherichia coli acid phosphatase. J Biol Chem 267 (1992) 22830-22836
17. Berka R.M., Gray G.L., and Vasil M.L. Studies of phospholipase C (heat labile hemolysin) in Pseudomonas aeruginosa. Infect Immun 34 (1981) 1071-1074
18. Gort A.S., and Imlay J.A. Balance between endogenous superoxide stress and antioxidant defences. J Bacteriol 180 (1998) 1402-1410
19. Schwyn B., and Neilands J.B. Universal chemical assay for the detection and determination of siderophores. Anal Biochem 160 (1987) 47-56
20. Chavira R., Burnett T.J., and Hageman J.H. Assaying proteinases with azocoll. Anal Biochem 136 (1984) 446-450
21. Domenech C.E., Lisa T.A., Salvano M.A., and Garrido M.N. Pseudomonas aeruginosa acid phosphatase. Activation by divalent cations and inhibition by aluminium ion. FEBS Lett 299 (1992) 96-98
22. Pine L., Hoffman P.S., Malcolm G.B., Benson R.F., and Keen M.G. Determination of catalase, peroxidase, and superoxide dismutase within the genus Legionella. J Clin Microbiol 20 (1984) 421-429
23. Abrams J.J., and Webster D.A. Purification, partial characterization, and possible role of catalase in the bacterium Vitreoscilla. Arch Biochem Biophys 279 (1990) 54-59
24. Steinman H.M. Bacteriocuprein superoxide dismutase in pseudomonads. J Bacteriol 162 (1985) 1255-1260
25. Geoffroy C., Raveneau J., Beretti J.L., Lecroisey A., Vazquez-Boland J.A., Alouf J.E., et al. Purification and characterization of an extracellular 29 kilodalton phospholipase from Listeria monocytogenes. Infect Immun 59 (1991) 2382-2388
26. Shang H., Thong J.T., Gopalakrishnakone P., Lee M.A., Yap E.P., Moochhala S., et al. Production of oxalate in the culture supernate of Burkholderia pseudomallei. Med Microbiol 50 (2001) 655-656
27. Haubler S., Nimtz M., Domke T., Wray V., and Steinmetz I. Purification and characterization of a cytotoxic exolipid of Burkholderia pseudomallei. Infect Immun 66 (1998) 1588-1593
28. Haase A., Janzen J., Barrett S., and Currie B. Toxin production by Burkholderia pseudomallei strains and correlation with severity of melioidosis. J Med Microbiol 46 (1997) 557-563
29. Woods D.E., DeShazer D., Moore R.A., Brett P.J., Burtnick M.N., Reckseidler S.L., et al. Current studies on the pathogenesis of melioidosis. Microbes Infect 1 (1999) 157-162
30. Rechnitzer C., Williams A., Wright B.J., Dowsett A.B., Milman N., and Fitzgeorge R.B. Demonstration of the intracellular production of tissue destructive protease by Legionella pneumophila multiplying within guinea pig and human alveolar macrophage. J Gen Microbiol 138 (1992) 1671-1677
31. Mintz C.S., Miller R.D., Gutgsell N.S., and Malek T. Legionella pneumophila protease inactivates interleukin-2 and cleaves CD4 on human T cells. Infect Immun 61 (1993) 3416-3421
32. Rielly T.J., Baron G.S., Nano F.E., and Kuhlenschmidt M.S. Characterization and sequencing of a respiratory burst-inhibiting acid phosphatase from Francisella tularensis. J Biol Chem 271 (1996) 10973-10983
33. Korbsrisate S., Suwanasai N., Leelaporn A., Ezaki T., Kawamura Y., and Sarasombath S. Cloning and characterization of a nonhemolytic phospholipase C gene from Burkholderia pseudomallei. J Clin Microbiol 37 (1999) 3742-3745
34. Songer J.G. Bacterial phospholipases and their role in virulence. Trends Microbiol 5 (1997) 156-161
35. Smith G.A., Marquis H., Jones S., Johnston N.C., Portnoy D.A., and Goldfine H. The two distinct phospholipases C of Listeria monocytogenes have overlapping roles in escape from a vacuole and cell-to-cell spread. Infect Immun 63 (1995) 4231-4237
36. Wilson T.M., Lisle G.W., and Collins D.M. Effect of inhA and katG on isoniazid resistance and virulence of Mycobacterium bovis. Mol Microbiol 15 (1995) 1006-1015
37. Lefebre M.D., and Valvano M.A. In vitro resistance of Burkholderia cepacia complex isolates to reactive oxygen species in relation to catalase and superoxide dismutase production. Microbiol 147 (2001) 97-109
38. Ulett G.C., Currie B.J., Clair T.W., Mayo M., Ketheesan N., Labrooy J., et al. Burkholderia pseudomallei virulence: definition, stability and association with clonality. Microbes Infect 3 (2001) 621-631
39. De Melo M.A., Gabbiani G., and Pechere J.C. Cellular events and intracellular survival of Campylobacter jejuni during infection of HEp-2 cells. Infect Immun 57 (1989) 2214-2222
40. Fang F.C. Mechanisms of nitric oxide-related antimicrobial activity. J Clin Invest 99 (1997) 2818-2825
41. DeGroote M.A., Ochsner U.A., Shiloh M.A., Nathan C., McCord J.M., Dinauer M.C., et al. Periplasmic superoxide dismutase protects Salmonella from products of phagocyte NADPH-oxidase and nitric oxide synthase. Proc Natl Acad Sci USA 94 (1997) 13997-14001
42. Mohapatra N.P., Balagopal A., Soni S., Schlesinger L.S., and Gunn J.S. AcpA is a Francisella acid phosphatase that affects intramacrophage survival and virulence. Infect Immun 75 (2007) 390-396
43. Hassan H.M., Bhatti A., and White L.A. Superoxide dismutase, catalase and peroxidase in four strains of Neisseria meningitides of different virulence. FEMS Microbiol Lett 25 (1984) 71-74
44. Jepras R.I., and Fitzgeorge R.B. The effect of oxygen-dependant antimicrobial systems on strains of Legionella pneumophila of different virulence. J Hyg 97 (1986) 61-69
45. Zhang Y., Garbe T., and Young D. Transformation with katG restores isoniazid sensitivity in Mycobacterium tuberculosis isolates resistant to a range of drug concentrations. Mol Microbiol 8 (1993) 521-524
46. Kusner D.J. Mechanisms of mycobacterial persistence in tuberculosis. Clin Immunol 114 (2005) 239-247
47. Guan K., and Dixon J.E. Protein tyrosine phosphatase activity of an essential virulence determinant in Yersinia. Science 249 (1990) 553-556
48. Kaniga K., Uralil J., Bliska J.B., and Galan J.E. A secreted tyrosine phosphatase with modular effector domains in bacterial pathogen Salmonella typhimurium. Mol Microbiol 21 (1996) 633-641
49. Korbsrisate S., Vanaporn M., Kerdsuk P., Kespichayawattana W., Vattanaviboon P., Kiatpapan P., et al. The Burkholderia pseudomallei RpoE (AlgU) operon is involved in environmental stress tolerance and biofilm formation. FEMS Microbiol Lett 252 (2005) 243-249
50. Tuanyok A., Tom M., Dunbar J., and Woods D.E. Genome-wide expression analysis of Burkholderia pseudomallei infection in a hamster model of acute melioidosis. Infect Immun 74 (2006) 5465-5476
51. Johansen K.A., Gill R.E., and Vasil M.L. Biochemical and molecular analysis of phospholipase C and phospholipase D activity in mycobacteria. Infect Immun 64 (1996) 3259-3266
52. Plotkowski M.C., and Meirelles. Concomitant endosomes-phagosome fusion and lysis of endosomal membranes account for Pseudomonas aeruginosa in human endothelial cells. J Submicrosc Cytol Pathol 29 (1997) 229-237
53. Raynaud C., Etienne G., Peyron P., Laneelle M.A., and Daffe M. Extracellular enzyme activities potentially involved in the pathogenicity of Mycobacterium tuberculosis. Microbiol 144 (1998) 577-587