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. 1995 Jul;177(14):3998–4008. doi: 10.1128/jb.177.14.3998-4008.1995

Virulence factors are released from Pseudomonas aeruginosa in association with membrane vesicles during normal growth and exposure to gentamicin: a novel mechanism of enzyme secretion.

J L Kadurugamuwa 1, T J Beveridge 1
PMCID: PMC177130  PMID: 7608073

Abstract

Pseudomonas aeruginosa blebs-off membrane vesicles (MVs) into culture medium during normal growth. Release of these vesicles increased approximately threefold after exposure of the organism to four times the MIC of gentamicin. Natural and gentamicin-induced membrane vesicles (n-MVs and g-MVs and g-MVs, respectively) were isolated by filtration and differential centrifugation, and several of their biological activities were characterized. Electron microscopy of both n-MVs and g-MVs revealed that they were spherical bilayer MVs with a diameter of 50 to 150 nm. Immunoelectron microscopy and Western blot (immunoblot) analysis of the vesicles demonstrated the presence of B-band lipopolysaccharide (LPS), with a slightly higher proportion of B-band LPS in g-MVs than in n-MVs. A-band LPS was occasionally detected in g-MVs but not in n-MVs. In addition to LPS, several enzymes, such as phospholipase C, protease, hemolysin, and alkaline phosphatase, which are known to contribute to the pathogenicity of Pseudomonas infections were found to be present in both vesicle types. Both types of vesicles contained DNA, with a significantly higher content in g-MVs. These vesicles could thus play an important role in genetic transformation and disease by serving as a transport vehicle for DNA and virulence factors and are presumably involved in septic shock.

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Selected References

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  1. Bergmann U., Scheffer J., Köller M., Schönfeld W., Erbs G., Müller F. E., König W. Induction of inflammatory mediators (histamine and leukotrienes) from rat peritoneal mast cells and human granulocytes by Pseudomonas aeruginosa strains from burn patients. Infect Immun. 1989 Jul;57(7):2187–2195. doi: 10.1128/iai.57.7.2187-2195.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Berk R. S., Brown D., Coutinho I., Meyers D. In vivo studies with two phospholipase C fractions from Pseudomonas aeruginosa. Infect Immun. 1987 Jul;55(7):1728–1730. doi: 10.1128/iai.55.7.1728-1730.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berka R. M., Gray G. L., Vasil M. L. Studies of phospholipase C (heat-labile hemolysin) in Pseudomonas aeruginosa. Infect Immun. 1981 Dec;34(3):1071–1074. doi: 10.1128/iai.34.3.1071-1074.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bever R. A., Iglewski B. H. Molecular characterization and nucleotide sequence of the Pseudomonas aeruginosa elastase structural gene. J Bacteriol. 1988 Sep;170(9):4309–4314. doi: 10.1128/jb.170.9.4309-4314.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brito N., Falcón M. A., Carnicero A., Gutiérrez-Navarro A. M., Mansito T. B. Purification and peptidase activity of a bacteriolytic extracellular enzyme from Pseudomonas aeruginosa. Res Microbiol. 1989 Feb;140(2):125–137. doi: 10.1016/0923-2508(89)90046-6. [DOI] [PubMed] [Google Scholar]
  6. Cadieux J. E., Kuzio J., Milazzo F. H., Kropinski A. M. Spontaneous release of lipopolysaccharide by Pseudomonas aeruginosa. J Bacteriol. 1983 Aug;155(2):817–825. doi: 10.1128/jb.155.2.817-825.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dorward D. W., Garon C. F., Judd R. C. Export and intercellular transfer of DNA via membrane blebs of Neisseria gonorrhoeae. J Bacteriol. 1989 May;171(5):2499–2505. doi: 10.1128/jb.171.5.2499-2505.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Duong F., Lazdunski A., Cami B., Murgier M. Sequence of a cluster of genes controlling synthesis and secretion of alkaline protease in Pseudomonas aeruginosa: relationships to other secretory pathways. Gene. 1992 Nov 2;121(1):47–54. doi: 10.1016/0378-1119(92)90160-q. [DOI] [PubMed] [Google Scholar]
  9. Fecycz I. T., Campbell J. N. Mechanisms of activation and secretion of a cell-associated precursor of an exocellular protease of Pseudomonas aeruginosa 34362A. Eur J Biochem. 1985 Jan 2;146(1):35–42. doi: 10.1111/j.1432-1033.1985.tb08616.x. [DOI] [PubMed] [Google Scholar]
  10. Filloux A., Bally M., Ball G., Akrim M., Tommassen J., Lazdunski A. Protein secretion in gram-negative bacteria: transport across the outer membrane involves common mechanisms in different bacteria. EMBO J. 1990 Dec;9(13):4323–4329. doi: 10.1002/j.1460-2075.1990.tb07881.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Govan J. R., Harris G. S. Pseudomonas aeruginosa and cystic fibrosis: unusual bacterial adaptation and pathogenesis. Microbiol Sci. 1986 Oct;3(10):302–308. [PubMed] [Google Scholar]
  12. Guzzo J., Pages J. M., Duong F., Lazdunski A., Murgier M. Pseudomonas aeruginosa alkaline protease: evidence for secretion genes and study of secretion mechanism. J Bacteriol. 1991 Sep;173(17):5290–5297. doi: 10.1128/jb.173.17.5290-5297.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hamood A. N., Ohman D. E., West S. E., Iglewski B. H. Isolation and characterization of toxin A excretion-deficient mutants of Pseudomonas aeruginosa PAO1. Infect Immun. 1992 Feb;60(2):510–517. doi: 10.1128/iai.60.2.510-517.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hancock R. E. Aminoglycoside uptake and mode of action--with special reference to streptomycin and gentamicin. I. Antagonists and mutants. J Antimicrob Chemother. 1981 Oct;8(4):249–276. doi: 10.1093/jac/8.4.249. [DOI] [PubMed] [Google Scholar]
  15. Hastie A. T., Hingley S. T., Kueppers F., Higgins M. L., Tannenbaum C. S., Weinbaum G. Protease production by Pseudomonas aeruginosa isolates from patients with cystic fibrosis. Infect Immun. 1983 May;40(2):506–513. doi: 10.1128/iai.40.2.506-513.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Howe T. R., Iglewski B. H. Isolation and characterization of alkaline protease-deficient mutants of Pseudomonas aeruginosa in vitro and in a mouse eye model. Infect Immun. 1984 Mar;43(3):1058–1063. doi: 10.1128/iai.43.3.1058-1063.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hurley J. C. Antibiotic-induced release of endotoxin: a reappraisal. Clin Infect Dis. 1992 Nov;15(5):840–854. doi: 10.1093/clind/15.5.840. [DOI] [PubMed] [Google Scholar]
  18. Ingram J. M., Cheng K. J., Costerton J. W. Alkaline phosphatase of Pseudomonas aeruginosa: the mechanism of secretion and release of the enzyme from whole cells. Can J Microbiol. 1973 Nov;19(11):1407–1415. doi: 10.1139/m73-227. [DOI] [PubMed] [Google Scholar]
  19. Kadurugamuwa J. L., Clarke A. J., Beveridge T. J. Surface action of gentamicin on Pseudomonas aeruginosa. J Bacteriol. 1993 Sep;175(18):5798–5805. doi: 10.1128/jb.175.18.5798-5805.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kadurugamuwa J. L., Hengstler B., Zak O. Cerebrospinal fluid protein profile in experimental pneumococcal meningitis and its alteration by ampicillin and anti-inflammatory agents. J Infect Dis. 1989 Jan;159(1):26–34. doi: 10.1093/infdis/159.1.26. [DOI] [PubMed] [Google Scholar]
  21. Kadurugamuwa J. L., Lam J. S., Beveridge T. J. Interaction of gentamicin with the A band and B band lipopolysaccharides of Pseudomonas aeruginosa and its possible lethal effect. Antimicrob Agents Chemother. 1993 Apr;37(4):715–721. doi: 10.1128/aac.37.4.715. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kahn M. E., Barany F., Smith H. O. Transformasomes: specialized membranous structures that protect DNA during Haemophilus transformation. Proc Natl Acad Sci U S A. 1983 Nov;80(22):6927–6931. doi: 10.1073/pnas.80.22.6927. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kellenberger E. The 'Bayer bridges' confronted with results from improved electron microscopy methods. Mol Microbiol. 1990 May;4(5):697–705. doi: 10.1111/j.1365-2958.1990.tb00640.x. [DOI] [PubMed] [Google Scholar]
  24. Kessler E., Safrin M., Olson J. C., Ohman D. E. Secreted LasA of Pseudomonas aeruginosa is a staphylolytic protease. J Biol Chem. 1993 Apr 5;268(10):7503–7508. [PubMed] [Google Scholar]
  25. Kessler E., Safrin M. Synthesis, processing, and transport of Pseudomonas aeruginosa elastase. J Bacteriol. 1988 Nov;170(11):5241–5247. doi: 10.1128/jb.170.11.5241-5247.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lazdunski A., Guzzo J., Filloux A., Bally M., Murgier M. Secretion of extracellular proteins by Pseudomonas aeruginosa. Biochimie. 1990 Feb-Mar;72(2-3):147–156. doi: 10.1016/0300-9084(90)90140-c. [DOI] [PubMed] [Google Scholar]
  27. Lightfoot J., Lam J. S. Molecular cloning of genes involved with expression of A-band lipopolysaccharide, an antigenically conserved form, in Pseudomonas aeruginosa. J Bacteriol. 1991 Sep;173(18):5624–5630. doi: 10.1128/jb.173.18.5624-5630.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Lory S. Determinants of extracellular protein secretion in gram-negative bacteria. J Bacteriol. 1992 Jun;174(11):3423–3428. doi: 10.1128/jb.174.11.3423-3428.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Martin N. L., Beveridge T. J. Gentamicin interaction with Pseudomonas aeruginosa cell envelope. Antimicrob Agents Chemother. 1986 Jun;29(6):1079–1087. doi: 10.1128/aac.29.6.1079. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Matsumoto K., Shams N. B., Hanninen L. A., Kenyon K. R. Cleavage and activation of corneal matrix metalloproteases by Pseudomonas aeruginosa proteases. Invest Ophthalmol Vis Sci. 1993 May;34(6):1945–1953. [PubMed] [Google Scholar]
  31. Mayrand D., Holt S. C. Biology of asaccharolytic black-pigmented Bacteroides species. Microbiol Rev. 1988 Mar;52(1):134–152. doi: 10.1128/mr.52.1.134-152.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Mustafa M. M., Mertsola J., Ramilo O., Sáez-Llorens X., Risser R. C., McCracken G. H., Jr Increased endotoxin and interleukin-1 beta concentrations in cerebrospinal fluid of infants with coliform meningitis and ventriculitis associated with intraventricular gentamicin therapy. J Infect Dis. 1989 Nov;160(5):891–895. doi: 10.1093/infdis/160.5.891. [DOI] [PubMed] [Google Scholar]
  33. Ngeleka M., Beauchamp D., Tardif D., Auclair P., Gourde P., Bergeron M. G. Endotoxin increases the nephrotoxic potential of gentamicin and vancomycin plus gentamicin. J Infect Dis. 1990 Apr;161(4):721–727. doi: 10.1093/infdis/161.4.721. [DOI] [PubMed] [Google Scholar]
  34. Prins J. M., van Deventer S. J., Kuijper E. J., Speelman P. Clinical relevance of antibiotic-induced endotoxin release. Antimicrob Agents Chemother. 1994 Jun;38(6):1211–1218. doi: 10.1128/aac.38.6.1211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Pugsley A. P. The complete general secretory pathway in gram-negative bacteria. Microbiol Rev. 1993 Mar;57(1):50–108. doi: 10.1128/mr.57.1.50-108.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Rivera M., Bryan L. E., Hancock R. E., McGroarty E. J. Heterogeneity of lipopolysaccharides from Pseudomonas aeruginosa: analysis of lipopolysaccharide chain length. J Bacteriol. 1988 Feb;170(2):512–521. doi: 10.1128/jb.170.2.512-521.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Shortridge V. D., Lazdunski A., Vasil M. L. Osmoprotectants and phosphate regulate expression of phospholipase C in Pseudomonas aeruginosa. Mol Microbiol. 1992 Apr;6(7):863–871. doi: 10.1111/j.1365-2958.1992.tb01537.x. [DOI] [PubMed] [Google Scholar]
  38. Strominger J. L., Ghuysen J. M. Mechanisms of enzymatic bacteriaolysis. Cell walls of bacteri are solubilized by action of either specific carbohydrases or specific peptidases. Science. 1967 Apr 14;156(3772):213–221. doi: 10.1126/science.156.3772.213. [DOI] [PubMed] [Google Scholar]
  39. Tan A. S., Worobec E. A. Isolation and characterization of two immunochemically distinct alkaline phosphatases from Pseudomonas aeruginosa. FEMS Microbiol Lett. 1993 Feb 1;106(3):281–286. doi: 10.1111/j.1574-6968.1993.tb05977.x. [DOI] [PubMed] [Google Scholar]
  40. Tuomanen E., Liu H., Hengstler B., Zak O., Tomasz A. The induction of meningeal inflammation by components of the pneumococcal cell wall. J Infect Dis. 1985 May;151(5):859–868. doi: 10.1093/infdis/151.5.859. [DOI] [PubMed] [Google Scholar]
  41. Turner L. R., Lara J. C., Nunn D. N., Lory S. Mutations in the consensus ATP-binding sites of XcpR and PilB eliminate extracellular protein secretion and pilus biogenesis in Pseudomonas aeruginosa. J Bacteriol. 1993 Aug;175(16):4962–4969. doi: 10.1128/jb.175.16.4962-4969.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Vaara M. Agents that increase the permeability of the outer membrane. Microbiol Rev. 1992 Sep;56(3):395–411. doi: 10.1128/mr.56.3.395-411.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Vasil M. L., Graham L. M., Ostroff R. M., Shortridge V. D., Vasil A. I. Phospholipase C: molecular biology and contribution to the pathogenesis of Pseudomonas aeruginosa. Antibiot Chemother (1971) 1991;44:34–47. doi: 10.1159/000420295. [DOI] [PubMed] [Google Scholar]
  44. Walker S. G., Beveridge T. J. Amikacin disrupts the cell envelope of Pseudomonas aeruginosa ATCC 9027. Can J Microbiol. 1988 Jan;34(1):12–18. doi: 10.1139/m88-003. [DOI] [PubMed] [Google Scholar]
  45. Wandersman C. Secretion across the bacterial outer membrane. Trends Genet. 1992 Sep;8(9):317–322. doi: 10.1016/0168-9525(92)90264-5. [DOI] [PubMed] [Google Scholar]
  46. Whitmire W. M., Garon C. F. Specific and nonspecific responses of murine B cells to membrane blebs of Borrelia burgdorferi. Infect Immun. 1993 Apr;61(4):1460–1467. doi: 10.1128/iai.61.4.1460-1467.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Wispelwey B., Hansen E. J., Scheld W. M. Haemophilus influenzae outer membrane vesicle-induced blood-brain barrier permeability during experimental meningitis. Infect Immun. 1989 Aug;57(8):2559–2562. doi: 10.1128/iai.57.8.2559-2562.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Wong K. R., Buckley J. T. Proton motive force involved in protein transport across the outer membrane of Aeromonas salmonicida. Science. 1989 Nov 3;246(4930):654–656. doi: 10.1126/science.2814486. [DOI] [PubMed] [Google Scholar]
  49. Wretlind B., Pavlovskis O. R. Pseudomonas aeruginosa elastase and its role in pseudomonas infections. Rev Infect Dis. 1983 Nov-Dec;5 (Suppl 5):S998–1004. doi: 10.1093/clinids/5.supplement_5.s998. [DOI] [PubMed] [Google Scholar]

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