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. 1997 Dec;65(12):4972–4977. doi: 10.1128/iai.65.12.4972-4977.1997

Identification and characterization of a two-component regulatory system involved in invasion of eukaryotic cells and heavy-metal resistance in Burkholderia pseudomallei.

A L Jones 1, D DeShazer 1, D E Woods 1
PMCID: PMC175717  PMID: 9393784

Abstract

Burkholderia pseudomallei is the causative agent of melioidosis, a disease increasingly recognized as an important cause of morbidity and mortality in many regions of the world. B. pseudomallei is a facultative intracellular pathogen capable of invading eukaryotic cells. We used Tn5-OT182 mutagenesis to generate mutants deficient in the ability to invade a human type II pneumocyte cell line (A549 cells). One of these mutants, AJ1D8, exhibited approximately 10% of the ability of the parental strain, 1026b, to invade A549 cells. There was no difference in the abilities of 1026b and AJ1D8 to resist killing by RAW macrophages or the human defensin HNP-1. The nucleotide sequence flanking the Tn5-OT182 integration in AJ1D8 was determined, and two open reading frames were identified. The predicted proteins shared considerable homology with two-component regulatory systems involved in the regulation of heavy-metal resistance in other organisms. AJ1D8 was 16-fold more sensitive to Cd2+ and twofold more sensitive to Zn2+ than was 1026b but was not sensitive to any of the other heavy metals examined. The B. pseudomallei two-component regulatory system, termed irlRS, complemented the invasion-deficient and heavy-metal-sensitive phenotype of AJ1D8 in trans. There was no significant difference between the virulence of AJ1D8 and that of 1026b in infant diabetic rats and Syrian hamsters, suggesting that the irlRS locus is probably not a virulence determinant in these animal models of acute B. pseudomallei infection.

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Selected References

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  1. Ashdown L. R., Koehler J. M. Production of hemolysin and other extracellular enzymes by clinical isolates of Pseudomonas pseudomallei. J Clin Microbiol. 1990 Oct;28(10):2331–2334. doi: 10.1128/jcm.28.10.2331-2334.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bowe F., Heffron F. Isolation of Salmonella mutants defective for intracellular survival. Methods Enzymol. 1994;236:509–526. doi: 10.1016/0076-6879(94)36039-1. [DOI] [PubMed] [Google Scholar]
  3. Boyer H. W., Roulland-Dussoix D. A complementation analysis of the restriction and modification of DNA in Escherichia coli. J Mol Biol. 1969 May 14;41(3):459–472. doi: 10.1016/0022-2836(69)90288-5. [DOI] [PubMed] [Google Scholar]
  4. Brett P. J., Deshazer D., Woods D. E. Characterization of Burkholderia pseudomallei and Burkholderia pseudomallei-like strains. Epidemiol Infect. 1997 Apr;118(2):137–148. doi: 10.1017/s095026889600739x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brett P. J., Mah D. C., Woods D. E. Isolation and characterization of Pseudomonas pseudomallei flagellin proteins. Infect Immun. 1994 May;62(5):1914–1919. doi: 10.1128/iai.62.5.1914-1919.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Brett P. J., Woods D. E. Structural and immunological characterization of Burkholderia pseudomallei O-polysaccharide-flagellin protein conjugates. Infect Immun. 1996 Jul;64(7):2824–2828. doi: 10.1128/iai.64.7.2824-2828.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Brown N. L., Barrett S. R., Camakaris J., Lee B. T., Rouch D. A. Molecular genetics and transport analysis of the copper-resistance determinant (pco) from Escherichia coli plasmid pRJ1004. Mol Microbiol. 1995 Sep;17(6):1153–1166. doi: 10.1111/j.1365-2958.1995.mmi_17061153.x. [DOI] [PubMed] [Google Scholar]
  8. Chaowagul W., White N. J., Dance D. A., Wattanagoon Y., Naigowit P., Davis T. M., Looareesuwan S., Pitakwatchara N. Melioidosis: a major cause of community-acquired septicemia in northeastern Thailand. J Infect Dis. 1989 May;159(5):890–899. doi: 10.1093/infdis/159.5.890. [DOI] [PubMed] [Google Scholar]
  9. Dance D. A. Melioidosis: the tip of the iceberg? Clin Microbiol Rev. 1991 Jan;4(1):52–60. doi: 10.1128/cmr.4.1.52. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dance D. A. Pseudomonas pseudomallei: danger in the paddy fields. Trans R Soc Trop Med Hyg. 1991 Jan-Feb;85(1):1–3. doi: 10.1016/0035-9203(91)90134-k. [DOI] [PubMed] [Google Scholar]
  11. DeShazer D., Brett P. J., Carlyon R., Woods D. E. Mutagenesis of Burkholderia pseudomallei with Tn5-OT182: isolation of motility mutants and molecular characterization of the flagellin structural gene. J Bacteriol. 1997 Apr;179(7):2116–2125. doi: 10.1128/jb.179.7.2116-2125.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Egan A. M., Gordon D. L. Burkholderia pseudomallei activates complement and is ingested but not killed by polymorphonuclear leukocytes. Infect Immun. 1996 Dec;64(12):4952–4959. doi: 10.1128/iai.64.12.4952-4959.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Eickhoff T. C., Bennett J. V., Hayes P. S., Feeley J. Pseudomonas pseudomallei: susceptibility to chemotherapeutic agents. J Infect Dis. 1970 Feb;121(2):95–102. doi: 10.1093/infdis/121.2.95. [DOI] [PubMed] [Google Scholar]
  15. Harwig S. S., Ganz T., Lehrer R. I. Neutrophil defensins: purification, characterization, and antimicrobial testing. Methods Enzymol. 1994;236:160–172. doi: 10.1016/0076-6879(94)36015-4. [DOI] [PubMed] [Google Scholar]
  16. Howe C., Sampath A., Spotnitz M. The pseudomallei group: a review. J Infect Dis. 1971 Dec;124(6):598–606. doi: 10.1093/infdis/124.6.598. [DOI] [PubMed] [Google Scholar]
  17. Ismail G., Razak N., Mohamed R., Embi N., Omar O. Resistance of Pseudomonas pseudomallei to normal human serum bactericidal action. Microbiol Immunol. 1988;32(7):645–652. doi: 10.1111/j.1348-0421.1988.tb01426.x. [DOI] [PubMed] [Google Scholar]
  18. Jones A. L., Beveridge T. J., Woods D. E. Intracellular survival of Burkholderia pseudomallei. Infect Immun. 1996 Mar;64(3):782–790. doi: 10.1128/iai.64.3.782-790.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Koponen M. A., Zlock D., Palmer D. L., Merlin T. L. Melioidosis. Forgotten, but not gone! Arch Intern Med. 1991 Mar;151(3):605–608. doi: 10.1001/archinte.151.3.605. [DOI] [PubMed] [Google Scholar]
  20. Kyte J., Doolittle R. F. A simple method for displaying the hydropathic character of a protein. J Mol Biol. 1982 May 5;157(1):105–132. doi: 10.1016/0022-2836(82)90515-0. [DOI] [PubMed] [Google Scholar]
  21. Lieber M., Smith B., Szakal A., Nelson-Rees W., Todaro G. A continuous tumor-cell line from a human lung carcinoma with properties of type II alveolar epithelial cells. Int J Cancer. 1976 Jan 15;17(1):62–70. doi: 10.1002/ijc.2910170110. [DOI] [PubMed] [Google Scholar]
  22. Mackowiak P. A., Smith J. W. Septicemic melioidosis. Occurrence following acute influenza A six years after exposure in Vietnam. JAMA. 1978 Aug 25;240(8):764–766. doi: 10.1001/jama.240.8.764. [DOI] [PubMed] [Google Scholar]
  23. Madden T. L., Tatusov R. L., Zhang J. Applications of network BLAST server. Methods Enzymol. 1996;266:131–141. doi: 10.1016/s0076-6879(96)66011-x. [DOI] [PubMed] [Google Scholar]
  24. Mays E. E., Ricketts E. A. Melioidosis: recrudescence associated with bronchogenic carcinoma twenty-six years following initial geographic exposure. Chest. 1975 Aug;68(2):261–263. doi: 10.1378/chest.68.2.261. [DOI] [PubMed] [Google Scholar]
  25. Merriman T. R., Lamont I. L. Construction and use of a self-cloning promoter probe vector for gram-negative bacteria. Gene. 1993 Apr 15;126(1):17–23. doi: 10.1016/0378-1119(93)90585-q. [DOI] [PubMed] [Google Scholar]
  26. Mills S. D., Jasalavich C. A., Cooksey D. A. A two-component regulatory system required for copper-inducible expression of the copper resistance operon of Pseudomonas syringae. J Bacteriol. 1993 Mar;175(6):1656–1664. doi: 10.1128/jb.175.6.1656-1664.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Morrison R. E., Lamb A. S., Craig D. B., Johnson W. M. Melioidosis: a reminder. Am J Med. 1988 May;84(5):965–967. doi: 10.1016/0002-9343(88)90080-0. [DOI] [PubMed] [Google Scholar]
  28. Nies D. H. The cobalt, zinc, and cadmium efflux system CzcABC from Alcaligenes eutrophus functions as a cation-proton antiporter in Escherichia coli. J Bacteriol. 1995 May;177(10):2707–2712. doi: 10.1128/jb.177.10.2707-2712.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Pruksachartvuthi S., Aswapokee N., Thankerngpol K. Survival of Pseudomonas pseudomallei in human phagocytes. J Med Microbiol. 1990 Feb;31(2):109–114. doi: 10.1099/00222615-31-2-109. [DOI] [PubMed] [Google Scholar]
  30. Sexton M. M., Jones A. L., Chaowagul W., Woods D. E. Purification and characterization of a protease from Pseudomonas pseudomallei. Can J Microbiol. 1994 Nov;40(11):903–910. doi: 10.1139/m94-145. [DOI] [PubMed] [Google Scholar]
  31. Woods D. E., Jones A. L., Hill P. J. Interaction of insulin with Pseudomonas pseudomallei. Infect Immun. 1993 Oct;61(10):4045–4050. doi: 10.1128/iai.61.10.4045-4050.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Yabuuchi E., Kosako Y., Oyaizu H., Yano I., Hotta H., Hashimoto Y., Ezaki T., Arakawa M. Proposal of Burkholderia gen. nov. and transfer of seven species of the genus Pseudomonas homology group II to the new genus, with the type species Burkholderia cepacia (Palleroni and Holmes 1981) comb. nov. Microbiol Immunol. 1992;36(12):1251–1275. doi: 10.1111/j.1348-0421.1992.tb02129.x. [DOI] [PubMed] [Google Scholar]
  33. Yang H. M., Chaowagul W., Sokol P. A. Siderophore production by Pseudomonas pseudomallei. Infect Immun. 1991 Mar;59(3):776–780. doi: 10.1128/iai.59.3.776-780.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Yang H., Kooi C. D., Sokol P. A. Ability of Pseudomonas pseudomallei malleobactin to acquire transferrin-bound, lactoferrin-bound, and cell-derived iron. Infect Immun. 1993 Feb;61(2):656–662. doi: 10.1128/iai.61.2.656-662.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. van der Lelie D., Schwuchow T., Schwidetzky U., Wuertz S., Baeyens W., Mergeay M., Nies D. H. Two-component regulatory system involved in transcriptional control of heavy-metal homoeostasis in Alcaligenes eutrophus. Mol Microbiol. 1997 Feb;23(3):493–503. doi: 10.1046/j.1365-2958.1997.d01-1866.x. [DOI] [PubMed] [Google Scholar]

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