Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1995 Feb;63(2):585–590. doi: 10.1128/iai.63.2.585-590.1995

Use of adhesion-defective mutants of Staphylococcus aureus to define the role of specific plasma proteins in promoting bacterial adhesion to canine arteriovenous shunts.

P E Vaudaux 1, P François 1, R A Proctor 1, D McDevitt 1, T J Foster 1, R M Albrecht 1, D P Lew 1, H Wabers 1, S L Cooper 1
PMCID: PMC173036  PMID: 7822026

Abstract

We used an ex vivo canine arteriovenous shunt model, previously developed to study plasma protein adsorption and thrombogenesis on polymeric biomaterials, to define the role of host proteins in promoting adhesion of Staphylococcus aureus. Either polyethylene or polyvinyl chloride tubings were exposed to canine blood for 5, 15, or 60 min at a flow rate of 300 ml/min and then were flushed in phosphate-buffered saline (PBS), cut into 1.5-cm segments, and stored at -70 degrees C. After thawing, each segment was preincubated in 0.5% albumin in PBS to prevent nonspecific staphylococcal attachment to surfaces that were not exposed to blood. Each segment was then incubated with 4 x 10(6) CFU of [3H]thymidine-labelled S. aureus per ml for 60 min at 37 degrees C in an in vitro adhesion assay. Two site-specific mutants of S. aureus were tested: one specifically defective in adhesion to surface-bound fibronectin (FnAd-def) and the other defective in adhesion to fibrinogen (FgAD-def) [corrected]. Compared with their respective parental strains, the FgAd-def, but not the FnAd-def, mutant of S. aureus showed a strong (> 80%) decrease in attachment to ex vivo tubings. The adhesion of each strain of S. aureus onto polyethylene was consistently more than twofold higher than the adhesion onto polyvinyl chloride segments exposed to flowing blood for 5 or 15 min, but adhesion became similar to that on polyvinyl chloride after 60 min of exposure. In conclusion, the specific adhesion-defective mutants of S. aureus suggested that fibrinogen was the most active adhesion-promoting protein in a short-term blood-material interaction. The experimental approach described in this study should prove useful for screening materials thought to be resistant to protein-mediated staphylococcal adhesion and colonization.

Full Text

The Full Text of this article is available as a PDF (392.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bale M. D., Wohlfahrt L. A., Mosher D. F., Tomasini B., Sutton R. C. Identification of vitronectin as a major plasma protein adsorbed on polymer surfaces of different copolymer composition. Blood. 1989 Dec;74(8):2698–2706. [PubMed] [Google Scholar]
  2. Cheung A. L., Fischetti V. A. The role of fibrinogen in staphylococcal adherence to catheters in vitro. J Infect Dis. 1990 Jun;161(6):1177–1186. doi: 10.1093/infdis/161.6.1177. [DOI] [PubMed] [Google Scholar]
  3. Chhatwal G. S., Preissner K. T., Müller-Berghaus G., Blobel H. Specific binding of the human S protein (vitronectin) to streptococci, Staphylococcus aureus, and Escherichia coli. Infect Immun. 1987 Aug;55(8):1878–1883. doi: 10.1128/iai.55.8.1878-1883.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Collins W. E., Mosher D. F., Diwan A. R., Murthy K. D., Simmons S. R., Albrecht R. M., Cooper S. L. Ex vivo platelet deposition on fibronectin-preadsorbed surfaces. Scanning Microsc. 1987 Dec;1(4):1669–1676. [PubMed] [Google Scholar]
  5. Collins W. E., Mosher D. F., Tomasini B. R., Cooper S. L. A preliminary comparison of the thrombogenic activity of vitronectin and other RGD-containing proteins when bound to surfaces. Ann N Y Acad Sci. 1987;516:291–299. doi: 10.1111/j.1749-6632.1987.tb33049.x. [DOI] [PubMed] [Google Scholar]
  6. Cooper S. L., Fabrizius D. J., Grasel T. G. Methods of assessment of thrombosis ex vivo. Ann N Y Acad Sci. 1987;516:572–585. doi: 10.1111/j.1749-6632.1987.tb33074.x. [DOI] [PubMed] [Google Scholar]
  7. Flock J. I., Fröman G., Jönsson K., Guss B., Signäs C., Nilsson B., Raucci G., Hök M., Wadström T., Lindberg M. Cloning and expression of the gene for a fibronectin-binding protein from Staphylococcus aureus. EMBO J. 1987 Aug;6(8):2351–2357. doi: 10.1002/j.1460-2075.1987.tb02511.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Grasel T. G., Cooper S. L. Properties and biological interactions of polyurethane anionomers: effect of sulfonate incorporation. J Biomed Mater Res. 1989 Mar;23(3):311–338. doi: 10.1002/jbm.820230304. [DOI] [PubMed] [Google Scholar]
  9. Herrmann M., Lai Q. J., Albrecht R. M., Mosher D. F., Proctor R. A. Adhesion of Staphylococcus aureus to surface-bound platelets: role of fibrinogen/fibrin and platelet integrins. J Infect Dis. 1993 Feb;167(2):312–322. doi: 10.1093/infdis/167.2.312. [DOI] [PubMed] [Google Scholar]
  10. Herrmann M., Suchard S. J., Boxer L. A., Waldvogel F. A., Lew P. D. Thrombospondin binds to Staphylococcus aureus and promotes staphylococcal adherence to surfaces. Infect Immun. 1991 Jan;59(1):279–288. doi: 10.1128/iai.59.1.279-288.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Herrmann M., Vaudaux P. E., Pittet D., Auckenthaler R., Lew P. D., Schumacher-Perdreau F., Peters G., Waldvogel F. A. Fibronectin, fibrinogen, and laminin act as mediators of adherence of clinical staphylococcal isolates to foreign material. J Infect Dis. 1988 Oct;158(4):693–701. doi: 10.1093/infdis/158.4.693. [DOI] [PubMed] [Google Scholar]
  12. Holderbaum D., Spech T., Ehrhart L. A., Keys T., Hall G. S. Collagen binding in clinical isolates of Staphylococcus aureus. J Clin Microbiol. 1987 Dec;25(12):2258–2261. doi: 10.1128/jcm.25.12.2258-2261.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jönsson K., Signäs C., Müller H. P., Lindberg M. Two different genes encode fibronectin binding proteins in Staphylococcus aureus. The complete nucleotide sequence and characterization of the second gene. Eur J Biochem. 1991 Dec 18;202(3):1041–1048. doi: 10.1111/j.1432-1033.1991.tb16468.x. [DOI] [PubMed] [Google Scholar]
  14. Kuypers J. M., Proctor R. A. Reduced adherence to traumatized rat heart valves by a low-fibronectin-binding mutant of Staphylococcus aureus. Infect Immun. 1989 Aug;57(8):2306–2312. doi: 10.1128/iai.57.8.2306-2312.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lambrecht L. K., Young B. R., Stafford R. E., Park K., Albrecht R. M., Mosher D. F., Cooper S. L. The influence of preadsorbed canine von Willebrand factor, fibronectin and fibrinogen on ex vivo artificial surface-induced thrombosis. Thromb Res. 1986 Jan 1;41(1):99–117. doi: 10.1016/0049-3848(86)90283-5. [DOI] [PubMed] [Google Scholar]
  16. Lelah M. D., Lambrecht L. K., Cooper S. L. A canine ex vivo series shunt for evaluating thrombus deposition on polymer surfaces. J Biomed Mater Res. 1984 May-Jun;18(5):475–496. doi: 10.1002/jbm.820180503. [DOI] [PubMed] [Google Scholar]
  17. Liang O. D., Maccarana M., Flock J. I., Paulsson M., Preissner K. T., Wadström T. Multiple interactions between human vitronectin and Staphylococcus aureus. Biochim Biophys Acta. 1993 Nov 25;1225(1):57–63. doi: 10.1016/0925-4439(93)90122-h. [DOI] [PubMed] [Google Scholar]
  18. Lopes J. D., dos Reis M., Brentani R. R. Presence of laminin receptors in Staphylococcus aureus. Science. 1985 Jul 19;229(4710):275–277. doi: 10.1126/science.3160113. [DOI] [PubMed] [Google Scholar]
  19. McDevitt D., Francois P., Vaudaux P., Foster T. J. Molecular characterization of the clumping factor (fibrinogen receptor) of Staphylococcus aureus. Mol Microbiol. 1994 Jan;11(2):237–248. doi: 10.1111/j.1365-2958.1994.tb00304.x. [DOI] [PubMed] [Google Scholar]
  20. McDevitt D., Vaudaux P., Foster T. J. Genetic evidence that bound coagulase of Staphylococcus aureus is not clumping factor. Infect Immun. 1992 Apr;60(4):1514–1523. doi: 10.1128/iai.60.4.1514-1523.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Park K., Cooper S. L. Importance of composition of the initial protein layer and platelet spreading in acute surface-induced thrombosis. Trans Am Soc Artif Intern Organs. 1985;31:483–488. [PubMed] [Google Scholar]
  22. Park K., Gerndt S. J., Cooper S. L. The effect of fibrinogen sialic acid residues on ex vivo platelet deposition on biomaterials. Thromb Res. 1986 Aug 1;43(3):293–302. doi: 10.1016/0049-3848(86)90149-0. [DOI] [PubMed] [Google Scholar]
  23. Park K., Mosher D. F., Cooper S. L. Acute surface-induced thrombosis in the canine ex vivo model: importance of protein composition of the initial monolayer and platelet activation. J Biomed Mater Res. 1986 May-Jun;20(5):589–612. doi: 10.1002/jbm.820200506. [DOI] [PubMed] [Google Scholar]
  24. Patti J. M., Bremell T., Krajewska-Pietrasik D., Abdelnour A., Tarkowski A., Rydén C., Hök M. The Staphylococcus aureus collagen adhesin is a virulence determinant in experimental septic arthritis. Infect Immun. 1994 Jan;62(1):152–161. doi: 10.1128/iai.62.1.152-161.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Patti J. M., Jonsson H., Guss B., Switalski L. M., Wiberg K., Lindberg M., Hök M. Molecular characterization and expression of a gene encoding a Staphylococcus aureus collagen adhesin. J Biol Chem. 1992 Mar 5;267(7):4766–4772. [PubMed] [Google Scholar]
  26. Paulsson M., Wadström T. Vitronectin and type-I collagen binding by Staphylococcus aureus and coagulase-negative staphylococci. FEMS Microbiol Immunol. 1990 May;2(1):55–62. doi: 10.1111/j.1574-6968.1990.tb03479.x. [DOI] [PubMed] [Google Scholar]
  27. Peters W. R., Bush W. H., Jr, McIntyre R. D., Hill L. D. The development of fibrin sheath on indwelling venous catheters. Surg Gynecol Obstet. 1973 Jul;137(1):43–47. [PubMed] [Google Scholar]
  28. Phillips D. R., Fitzgerald L. A., Charo I. F., Parise L. V. The platelet membrane glycoprotein IIb/IIIa complex. Structure, function, and relationship to adhesive protein receptors in nucleated cells. Ann N Y Acad Sci. 1987;509:177–187. doi: 10.1111/j.1749-6632.1987.tb30994.x. [DOI] [PubMed] [Google Scholar]
  29. Raad I. I., Luna M., Khalil S. A., Costerton J. W., Lam C., Bodey G. P. The relationship between the thrombotic and infectious complications of central venous catheters. JAMA. 1994 Apr 6;271(13):1014–1016. [PubMed] [Google Scholar]
  30. Ruoslahti E., Hayman E. G., Pierschbacher M., Engvall E. Fibronectin: purification, immunochemical properties, and biological activities. Methods Enzymol. 1982;82(Pt A):803–831. doi: 10.1016/0076-6879(82)82103-4. [DOI] [PubMed] [Google Scholar]
  31. Toy P. T., Lai L. W., Drake T. A., Sande M. A. Effect of fibronectin on adherence of Staphylococcus aureus to fibrin thrombi in vitro. Infect Immun. 1985 Apr;48(1):83–86. doi: 10.1128/iai.48.1.83-86.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Vaudaux P. E., Waldvogel F. A., Morgenthaler J. J., Nydegger U. E. Adsorption of fibronectin onto polymethylmethacrylate and promotion of Staphylococcus aureus adherence. Infect Immun. 1984 Sep;45(3):768–774. doi: 10.1128/iai.45.3.768-774.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Vaudaux P., Pittet D., Haeberli A., Huggler E., Nydegger U. E., Lew D. P., Waldvogel F. A. Host factors selectively increase staphylococcal adherence on inserted catheters: a role for fibronectin and fibrinogen or fibrin. J Infect Dis. 1989 Nov;160(5):865–875. doi: 10.1093/infdis/160.5.865. [DOI] [PubMed] [Google Scholar]
  34. Vaudaux P., Pittet D., Haeberli A., Lerch P. G., Morgenthaler J. J., Proctor R. A., Waldvogel F. A., Lew D. P. Fibronectin is more active than fibrin or fibrinogen in promoting Staphylococcus aureus adherence to inserted intravascular catheters. J Infect Dis. 1993 Mar;167(3):633–641. doi: 10.1093/infdis/167.3.633. [DOI] [PubMed] [Google Scholar]
  35. Vaudaux P., Suzuki R., Waldvogel F. A., Morgenthaler J. J., Nydegger U. E. Foreign body infection: role of fibronectin as a ligand for the adherence of Staphylococcus aureus. J Infect Dis. 1984 Oct;150(4):546–553. doi: 10.1093/infdis/150.4.546. [DOI] [PubMed] [Google Scholar]
  36. Vaudaux P., Yasuda H., Velazco M. I., Huggler E., Ratti I., Waldvogel F. A., Lew D. P., Proctor R. A. Role of host and bacterial factors in modulating staphylococcal adhesion to implanted polymer surfaces. J Biomater Appl. 1990 Oct;5(2):134–153. doi: 10.1177/088532829000500204. [DOI] [PubMed] [Google Scholar]
  37. Vercellotti G. M., McCarthy J. B., Lindholm P., Peterson P. K., Jacob H. S., Furcht L. T. Extracellular matrix proteins (fibronectin, laminin, and type IV collagen) bind and aggregate bacteria. Am J Pathol. 1985 Jul;120(1):13–21. [PMC free article] [PubMed] [Google Scholar]
  38. Wang I. W., Anderson J. M., Marchant R. E. Staphylococcus epidermidis adhesion to hydrophobic biomedical polymer is mediated by platelets. J Infect Dis. 1993 Feb;167(2):329–336. doi: 10.1093/infdis/167.2.329. [DOI] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES