Inhibition by Immunoglobulins of Staphylococcus aureus Adherence to Fibronectin-Coated Foreign Surfaces

References

• Elek S D, Conen P E. The virulence of Staphylococcus pyogenes for man: A study of the problems of wound infection. Br JE J Exp Pathol 1957; 38: 573–586
   PubMed Web of Science ®Google Scholar
• James R C, MacLeod C J. Induction of staphylococcal infections in mice with small inocula introduced on sutures. Br J Exp Pathol 1961; 42: 266–277
   PubMedGoogle Scholar
• Noble W C. The production of subcutaneous staphylococcal skin lesions in mice. Br J Exp Pathol 1965; 46: 254–262
   PubMedGoogle Scholar
• Zimmerli W, Waldvogel F A, Vaudaux P. Pathogenesis of foreign body infection: Description and characteristics of an animal model. J Infect Dis 1982; 146: 487–497
   PubMed Web of Science ®Google Scholar
• Zimmerli W, Lew P D, Waldvogel F A. Pathogenesis of foreign body infection. Evidence for a local granulocyte defect. J Clin Invest 1984; 73: 1191–1200
   PubMed Web of Science ®Google Scholar
• Christensen G D, Simpson W A, Bisno A L. Adherence of slime-producing strains of Staphylococcus epidermidis to smooth surfaces. Infect Immun 1982; 37: 318–326
   PubMed Web of Science ®Google Scholar
• Peters G, Locci R, Pulverer G. Microbial colonization of prosthetic devices. II. Scanning electron microscopy of naturally infected catheters. Zentralbl Bakteriol Parasitenkd Hyg Abt 1 Orig Reihe B 1981; 173: 293–299
   PubMedGoogle Scholar
• Peters G, Locci R, Pulverer G. Adherence and growth of coagulase-negative staphylococci on surfaces of intravenous catheters. J Infect Dis 1982; 146: 293–299
   PubMedGoogle Scholar
• Costerton J W, Irvin R T, Cheng K J. The bacterial glycocalyz in nature and disease. Annu Rev Microbiol 1981; 35: 299–324
   PubMed Web of Science ®Google Scholar
• Gristina A G, Costerton J W. Bacterial adherence to biomaterials and tissues. J Bone Joint Surg 1985; 67A: 264–273
   Google Scholar
• Gray E D, Peters G, Vestergen M. Effects of extracellular slime substance from Staphylococcus epidermidis on the human cellular immune response. Lancet 1984; 1: 365–367
   PubMed Web of Science ®Google Scholar
• Johnson G M, Lee D A, Regelmann W E. Interference with granulocyte function by Staphylococcus epidermidis slime. Infect Immun 1986; 54: 13–20
   PubMed Web of Science ®Google Scholar
• Hawiger J, Timmons S, Strong D D. Identification of a region of human fibrinogen interacting with staphylococcal clumping factor. Biochemistry 1982; 21: 1407–1413
   PubMed Web of Science ®Google Scholar
• Lopez J D, Dos Reis M, Brentani R R. Presence of laminin receptors in. Staphylococcus aureus. Science 1985; 229: 275–277
   Google Scholar
• Vercelloti G M, McCarthy J B, Lindhom P. Extracellular matrix proteins (fibronectin laminin, and type IV collagen) bind and aggregate bacteria. Am J Pathol 1985; 120: 13–20
   PubMed Web of Science ®Google Scholar
• Holderbaum D, Spech R A, Erhadt L A. Specific binding sites of collagen to. Staphylococcus aureus. Coll Relat Res 1985; 5: 261–271
   PubMedGoogle Scholar
• Kuusela P. Fibronectin binds to. Staphylococcus aureus. Nature 1978; 276: 718–720
   Google Scholar
• Kuusela P, Vartio T, Vuento M. Binding sites for streptococci and staphylococci in fibronectin. Infect Immun 1984; 45: 433–436
   PubMed Web of Science ®Google Scholar
• Kuusela P, Vartio T, Vuento M. Attachment of staphylococci and streptococci on fibronectin, fibronectin fragments, and fibrinogen bound to a solid phase. Infect Immun 1985; 50: 77–81
   PubMed Web of Science ®Google Scholar
• Kuusela P, Vartio T, Vuento M. Time-resolved fluorimetry in the study of attachment of staphylococci and streptococci on substrate-bound fibronectin. FEMS Microbiol Letters 1986; 36: 57–62
   Web of Science ®Google Scholar
• Maxe I, Ryden C, Wadström T. Specific attachment of Staphylococcus aureus to immobilized fibronectin. Infect Immun 1986; 54: 695–704
   PubMed Web of Science ®Google Scholar
• Vercelloti G M, Lussenhop D, Peterson P K. Bacterial adherence to fibronectin and endothelial cells: A possible mechanism for bacterial tissue tropism. J Lab Clin Med 1984; 103: 34–43
   PubMedGoogle Scholar
• Vaudaux P, Suzuki R, Waldvogel F A. Foreign body infection: Role of fibronectin as a ligand for the adherence of. Staphylococcus aureus. J Infect Dis 1984; 150: 546–553
   PubMed Web of Science ®Google Scholar
• Vaudaux P E, Waldvogel F A, Morgenthaler J J. Adsorption of fibronectin onto polymethylmethacrylate and promotion of Staphylococcus aureus adherence. Infect Immun 1984; 45: 768–774
   PubMed Web of Science ®Google Scholar
• Römer J, Morgenthaler J J, Scherz R. Characterization of various immunoglobulin preparations for intravenous application. I. Protein composition and antibody content. Vox Sang 1982; 42: 62–73
   PubMed Web of Science ®Google Scholar
• Römer J, Spáth PJ, Skravil F. Characterization of various immunoglobulin preparations. II. Complement activation and binding to staphylococcus protein A. Vox Sang 1982; 42: 74–80
   PubMed Web of Science ®Google Scholar
• Spycher M O, Nydegger U E. Part of the activating cross-linked immunoglobulin G is internalized by human platelets to sites not accessible for enzymatic digestion. Blood 1986; 67: 12–18
   PubMed Web of Science ®Google Scholar
• Goding J W. Use of staphylococcal protein A as an immunological reagent. J Immunol Methods 1978; 20: 241–253
   PubMed Web of Science ®Google Scholar
• Langone J J, Boyle M DP, Borsos T. 125I protein A: Applications to the quantitative determination of fluid phase and cell-bound IgG. Scand J Immunol 1977; 18: 281–293
   Google Scholar
• Schleifer H, Kandler O. Zur chemischen Zusammensetzung der Zellwäande des Streptokokken. I. Zur Aminosäuresequenz des Mureins von. Str. thermophilus and Str. Faecalis. Arch Mikrobiol 1967; 57: 335–365
   PubMedGoogle Scholar
• Peterson P K, Wilkinson B J, Kim Y. The key role of peptidoglycan in the opsonization of. Staphylococcus aureus. J Clin Invest 1978; 61: 597–609
   PubMed Web of Science ®Google Scholar
• Verbrugh H A, Peters R, Rozenberg-Arska M. Antibodies to cell wall peptidoglycan of Staphylococcus aureus in patients with serious staphylococcal infections. J Infect Dis 1981; 144: 1–9
   PubMed Web of Science ®Google Scholar
• West T E, Cantey J R, Burdash N M. Enzyme-linked immunosorbent assay for detection of immunoglobulin G and M antibodies to teichoic acid in intravascular staphylococcal disease. Eur J Clin Microbiol 1985; 4: 286–290
   PubMedGoogle Scholar
• Kronvall G, Williams R C. Differences in anti-protein A activity among IgG subgroups. J Immunol 1969; 103: 828–833
   PubMed Web of Science ®Google Scholar
• Proctor R A, Mosher D F, Olbrantz P J. Fibronectin binding to. Staphylococcus aureus. J Biol Chem 1982; 257: 14,788–14,794
   Web of Science ®Google Scholar
• Ryden C, Rubin K, Speziale P. Fibronectin receptors from. Staphylococcus aureus. J Biol Chem 1983; 258: 3396–3401
   PubMed Web of Science ®Google Scholar
• Ekstedt R D. Immunity to the Staphylococci: The Staphylococci. Wiley, New York 1972; 385–418
   Google Scholar
• Jacob E, Arendt D M, Brook I. Enzyme-linked immunosorbent assay for detection of antibodies to Staphylococcus aureus cell walls in experimental osteomyelitis. J Clin Microbiol 1985; 22: 547–552
   PubMedGoogle Scholar
• Vaudaux P, Lew D, Waldvogel F A. Host-dependent pathogenic factors in foreign body infection: A comparison between. Staphylococcus epidermidis and S. aureus. Zentralbl Bakteriol Suppl 1987; 16: 183–193
   Google Scholar
• Svanborg-Eden C, Svennerholm A-M. Secretory immunoglobulin A and G antibodies prevent adhesion of Escherichia coli to human urinary tract epithelial cells. Infect Immun 1978; 22: 790–797
   PubMed Web of Science ®Google Scholar
• Tramont E C. Inhibition of adherence Neisseria gonorrhea by human genital secretions. J Clin Invest 1977; 59: 117–124
   PubMed Web of Science ®Google Scholar
• Abraham S N, Hasty D L, Simpton W A. Antiadhesive properties of a quaternary structure-specific hybridoma antibody against type 1 fimbriae of. Escherichia coli. J Exp Med 1983; 158: 1114–1128
   PubMedGoogle Scholar