Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1995 Aug;63(8):3143–3150. doi: 10.1128/iai.63.8.3143-3150.1995

Quantitative comparison of clumping factor- and coagulase-mediated Staphylococcus aureus adhesion to surface-bound fibrinogen under flow.

R B Dickinson 1, J A Nagel 1, D McDevitt 1, T J Foster 1, R A Proctor 1, S L Cooper 1
PMCID: PMC173429  PMID: 7622242

Abstract

The contributions of clumping factor and coagulase in mediating Staphylococcus aureus adhesion to surface-adsorbed fibrinogen have been quantified by using a new methodology and analysis. The attachment or detachment kinetics of bacteria were directly observed in a radial flow chamber with a well-defined laminar flow field and a spatially varying shear rate and were quantified by recursively scanning the chamber surface and counting cells via automated video microscopy and image analysis with a motorized stage and focus control. Intrinsic rate constants for attachment or detachment were estimated as functions of shear rate for the wild-type Newman strain of S. aureus and for mutants lacking clumping factor, coagulase, or both proteins on surfaces coated with plasma, fibrinogen, or albumin. Clumping factor, but not coagulase, increased the probability of attachment and decreased the probability of detachment of S. aureus on plasma-coated surfaces; however, both clumping factor and, to a lesser extent, coagulase increased the probability of attachment on the purified-fibrinogen-coated surface. All mutants were resistant to detachment on the purified-fibrinogen-coated surface, suggesting the possibility of an additional adhesion mechanism which was independent of coagulase or clumping factor and effective only for fully attached cells. Together, these results suggest that the presence of clumping factor plays the primary role in enhancing adhesion to surfaces with adsorbed fibrinogen, not only by enhancing the probability of cell attachment but also by increasing the strength of the resulting adhesion.

Full Text

The Full Text of this article is available as a PDF (373.6 KB).

Selected References

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

  1. Andrade J. D., Hlady V. Plasma protein adsorption: the big twelve. Ann N Y Acad Sci. 1987;516:158–172. doi: 10.1111/j.1749-6632.1987.tb33038.x. [DOI] [PubMed] [Google Scholar]
  2. Bodén M. K., Flock J. I. Cloning and characterization of a gene for a 19 kDa fibrinogen-binding protein from Staphylococcus aureus. Mol Microbiol. 1994 May;12(4):599–606. doi: 10.1111/j.1365-2958.1994.tb01046.x. [DOI] [PubMed] [Google Scholar]
  3. Bodén M. K., Flock J. I. Evidence for three different fibrinogen-binding proteins with unique properties from Staphylococcus aureus strain Newman. Microb Pathog. 1992 Apr;12(4):289–298. doi: 10.1016/0882-4010(92)90047-r. [DOI] [PubMed] [Google Scholar]
  4. Bodén M. K., Flock J. I. Fibrinogen-binding protein/clumping factor from Staphylococcus aureus. Infect Immun. 1989 Aug;57(8):2358–2363. doi: 10.1128/iai.57.8.2358-2363.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brückler J., Schaeg W., Blobel H. Isolierung des "Clumping Factors" von Staphylococcus aureus. Zentralbl Bakteriol Orig A. 1974 Sep;228(4):465–473. [PubMed] [Google Scholar]
  6. 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]
  7. Cozens-Roberts C., Lauffenburger D. A., Quinn J. A. Receptor-mediated cell attachment and detachment kinetics. I. Probabilistic model and analysis. Biophys J. 1990 Oct;58(4):841–856. doi: 10.1016/S0006-3495(90)82430-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. DUTHIE E. S., LORENZ L. L. Staphylococcal coagulase; mode of action and antigenicity. J Gen Microbiol. 1952 Feb;6(1-2):95–107. doi: 10.1099/00221287-6-1-2-95. [DOI] [PubMed] [Google Scholar]
  9. Davison V. E., Sanford B. A. Factors influencing adherence of Staphylococcus aureus to influenza A virus-infected cell cultures. Infect Immun. 1982 Sep;37(3):946–955. doi: 10.1128/iai.37.3.946-955.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Delmi M., Vaudaux P., Lew D. P., Vasey H. Role of fibronectin in staphylococcal adhesion to metallic surfaces used as models of orthopaedic devices. J Orthop Res. 1994 May;12(3):432–438. doi: 10.1002/jor.1100120316. [DOI] [PubMed] [Google Scholar]
  11. Dougherty S. H. Pathobiology of infection in prosthetic devices. Rev Infect Dis. 1988 Nov-Dec;10(6):1102–1117. doi: 10.1093/clinids/10.6.1102. [DOI] [PubMed] [Google Scholar]
  12. Espersen F., Clemmensen I., Barkholt V. Isolation of Staphylococcus aureus clumping factor. Infect Immun. 1985 Sep;49(3):700–708. doi: 10.1128/iai.49.3.700-708.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Goldsmith H. L., Turitto V. T. Rheological aspects of thrombosis and haemostasis: basic principles and applications. ICTH-Report--Subcommittee on Rheology of the International Committee on Thrombosis and Haemostasis. Thromb Haemost. 1986 Jun 30;55(3):415–435. [PubMed] [Google Scholar]
  14. Gristina A. G. Biomaterial-centered infection: microbial adhesion versus tissue integration. Science. 1987 Sep 25;237(4822):1588–1595. doi: 10.1126/science.3629258. [DOI] [PubMed] [Google Scholar]
  15. Hawiger J., Hammond D. K., Timmons S., Budzynski A. Z. Interaction of human fibrinogen with staphylococci: presence of a binding region on normal and abnormal fibrinogen variants and fibrinogen derivatives. Blood. 1978 May;51(5):799–812. [PubMed] [Google Scholar]
  16. Hawiger J., Kloczewiak M., Timmons S., Strong D., Doolittle R. F. Interaction of fibrinogen with staphylococcal clumping factor and with platelets. Ann N Y Acad Sci. 1983 Jun 27;408:521–535. doi: 10.1111/j.1749-6632.1983.tb23270.x. [DOI] [PubMed] [Google Scholar]
  17. 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]
  18. 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]
  19. Kuusela P., Vartio T., Vuento M., Myhre E. B. Attachment of staphylococci and streptococci on fibronectin, fibronectin fragments, and fibrinogen bound to a solid phase. Infect Immun. 1985 Oct;50(1):77–81. doi: 10.1128/iai.50.1.77-81.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kuusela P., Vartio T., Vuento M., Myhre E. B. Binding sites for streptococci and staphylococci in fibronectin. Infect Immun. 1984 Aug;45(2):433–436. doi: 10.1128/iai.45.2.433-436.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. 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]
  22. 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]
  23. McGavin M. H., Krajewska-Pietrasik D., Rydén C., Hök M. Identification of a Staphylococcus aureus extracellular matrix-binding protein with broad specificity. Infect Immun. 1993 Jun;61(6):2479–2485. doi: 10.1128/iai.61.6.2479-2485.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Mohammad S. F., Topham N. S., Burns G. L., Olsen D. B. Enhanced bacterial adhesion on surfaces pretreated with fibrinogen and fibronectin. ASAIO Trans. 1988 Jul-Sep;34(3):573–577. [PubMed] [Google Scholar]
  25. Ohtomo T., Yoshida K. Adhesion of Staphylococcus aureus to fibrinogen, collagen and lectin in relation to cell surface structure. Zentralbl Bakteriol Mikrobiol Hyg A. 1988 May;268(3):325–340. doi: 10.1016/s0176-6724(88)80017-8. [DOI] [PubMed] [Google Scholar]
  26. Proctor R. A., Mosher D. F., Olbrantz P. J. Fibronectin binding to Staphylococcus aureus. J Biol Chem. 1982 Dec 25;257(24):14788–14794. [PubMed] [Google Scholar]
  27. Saterbak A., Kuo S. C., Lauffenburger D. A. Heterogeneity and probabilistic binding contributions to receptor-mediated cell detachment kinetics. Biophys J. 1993 Jul;65(1):243–252. doi: 10.1016/S0006-3495(93)81077-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Usui Y. Biochemical properties of fibrinogen binding protein (clumping factor) of the staphylococcal cell surface. Zentralbl Bakteriol Mikrobiol Hyg A. 1986 Sep;262(3):287–297. doi: 10.1016/s0176-6724(86)80001-3. [DOI] [PubMed] [Google Scholar]
  29. 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]
  30. 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]

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

RESOURCES