Fibronectin, fibrinogen, and laminin act as mediators of adherence of clinical staphylococcal isolates to foreign material

Journal of Infectious Diseases

Volumn 158, Issue 4, 1988, Pages 693-701

  Herrmann, Mathias ^a,b   Vaudaux, Pierre E ^a,b   Pittet, Didier ^a,b   Auckenthaler, Raymond ^a,b   Daniel Lew, P ^a,b   Schumacher Perdreau, Françoise ^a,b   Peters, Georg ^a,b   Waldvogel, Francis A ^a,b  

^a UNIVERSITY HOSPITAL   (Switzerland)

^b UNIVERSITY OF COLOGNE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

FIBRINOGEN; FIBRONECTIN; LAMININ; PLASMA PROTEIN; RADIOISOTOPE;

BACTEREMIA; CELL ADHESION; COAGULASE NEGATIVE STAPHYLOCOCCUS; NONHUMAN; PRIORITY JOURNAL; STAPHYLOCOCCUS AUREUS;

BACTERIAL ADHESION; FIBRINOGEN; FIBRONECTINS; HUMAN; LAMININ; POLYMERS; SEPTICEMIA; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS; STAPHYLOCOCCUS AUREUS; SUPPORT, NON-U.S. GOV'T;

EID: 0023696405     PISSN: 00221899     EISSN: 15376613     Source Type: Journal    
DOI: 10.1093/infdis/158.4.693     Document Type: Article

References (63)

1. Quie PG, Belani KK. Coagulase-negative staphylococcal adherence and persistence. J Infect Dis 1987;156:543-7.
2. Baier RE. The organization of blood components near interfaces. Ann NY Acad Sci 1977;283:17-36.
3. Cottonaro CN, Roohk HV, Shimizu G, Sperling DR. Quantitation and characterization of competitive protein binding to polymers. Transactions of the American Society for Artifical Internal Organs 1981;27:391-5.
4. Kochwa S, Litwak RS, Rosenfield RE, Leonard EF. Blood elements at foreign surfaces: A biochemical approach to the study of the adsorption of plasma proteins. Ann NY Acad Sci 1977;283:37-49.
5. Hawiger J, Hammond DK, Timmons S, Budzynski AZ. Interaction of human fibrinogen with staphylococci: Presence of a binding region on normal and abnormal fibrinogen variants and fibrinogen derivatives. Blood 1978;51: 799-812.
6. Kuusela P. Fibronectin binds to Staphylococcus aureus. Nature 1978;276:718-20.
7. Lopes JD, dos Reis M, Brentani RR. Presence of laminin receptors in Staphylococcus aureus. Science 1985;229:275-7.
8. Ashkenazi S, Mirelman D. Adherence of bacteria to pediatric intravenous catheters and needles and its relation to phlebitis in animals. Pediatr Res 1984;18:1361-6.
9. Franson TR, Sheth NK, Rose HD, Sohnle PG. Quantitative adherence in vitro of coagulase-negative staphylococci to intravascular catheters: Inhibition with D-mannosamine. J Infect Dis 1984;149:116.
10. Hogt AH, Dankert J, Feijen J. Adhesion of coagulase-negative staphylococci to methacrylate polymers and copolymers. J Biomed Mater Res 1986;20:533-45.
11. Dankert J, Hogt AH, Jeijen J. Biomedical polymers: Bacterial adhesion, colonization, and infection. CRC Critical Reviews of Biocompatibility 1986;2:219-301.
12. Peters G, Locci R, Pulverer G. Adherence and growth of coagulase-negative staphylococci on surfaces of intravenous catheters. J Infect Dis 1982;146:479-82.
13. Vaudaux P, Suzuki R, Waldvogel FA, Morgenthaler JJ, Nydegger UE. Foreign body infection: Role of fibronectin as a ligand for the adherence of Staphylococcus aureus. J Infect Dis 1984;150:546-53.
14. Maxe I, Ryéin C, Wadström T, Rubin K. Specific attachment of Staphylococcus aureus adherence. Infect Immun 1986;54:695-704.
15. Vaudaux PE, Waldvogel FA, Morgenthaler JJ, Nydegger UE. Adsorption of fibronectin onto polymethylmethacrylate and promotion of Staphylococcus aureus adherence. Infect Immun 1984;45:768-74.
16. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 227:680-5.
17. Kloos WE, Schleifer KH. Genus IV. Staphylococcus. In: Sneath PHA, Mair NS, Sharpe ME, Holt JG, eds. Bergey’s manual of systematic bacteriology. Vol. 2. Baltimore: William & Wilkins, 1986:1013-35.
18. Christensen GD, Simpson WA, Bisno AL, Beachey EH. Adherence of slime-producing strains of Staphylococcus epidermidis to smooth surfaces. Infect Immun 1982;37: 318-26.
19. Christensen GD, Simpson WA, Younger JJ, Baddour LM, Barrett FF, Melton DM, Beachey EH. Adherence of coagulase-negative staphylococci to plastic tissue culture plates: A quantitative model for the adherence of staphylococci to medical devices. J Clin Microbiol 1985;22: 996-1006.
20. Falcieri E, Vaudaux P, Huggler E, Lew D, Waldvogel F. Role of bacterial exopolymers and host factors on adherence and phagocytosis of Staphylococcus aureus in foreign body infection. J Infect Dis 1987;155:524-31.
21. Lindon JN, McManama G, Kushner L, Merrill EW, Salzman EW. Does the conformation of adsorbed fibrinogen dictate platelet interactions with artificial surfaces? Blood 1986;68:355-62.
22. Vercellotti GM, McCarthy JB, Lindholm P, Peterson PK, Jacob HS, Furcht LT. Extracellular matrix proteins (fibronectin, laminin, and type IV collagen) bind and aggregate bacteria. Am J Pathol 1985;120:13-21.
23. Fuller RA, Rosen JJ. Materials for medicine. Sci Am 1986; 255:118-25.
24. Murabayashi S, Nos6 Y. Biocompatibility: Bioengineering aspects. Artificial Organs 1986;10:114-21.
25. Vaudaux P, Lerch P, Velazco MI, Nydegger UE, Waldvogel FA. Role of fibronectin in the susceptibility of biomaterial implants to bacterial infections. In: Christel P, Meunier A, Lee AJC, eds. Biological and biomedical performance of biomaterials. Amsterdam: Elsevier, 1986:355-60.
26. Hogt AH, Dankert J, Feijen J. Adhesion of Staphylococcus epidermidis and Staphylococcus saprophyticus to a hydrophobic biomaterial. J Gen Microbiol 1985;131:2485-91.
27. Fletcher M, Marshall KC. Bubble contact angle method for evaluating substratum interfacial characteristics and its relevance to bacterial attachment. Appl Environ Microbiol 1982;44:184-92.
28. Vaudaux PE, Lew D, Waldvogel FA. Host-dependent pathogenic factors in foreign body infection. A comparison between Staphylococcus epidermidis and S. aureus. In: Pulverer G, Quie PG, Peters G, eds. Pathogenicity and clinical significance of coagulase-negative staphylococci. Stuttgart, FRG: Gustav Fisher Verlag, 1987:183-93.
29. Rydén C, Rubin K, Speziale P, Höök M, Lindberg M, Wadström T. Fibronectin receptors from Staphylococcus aureus. J Biol Chem 1983;258:3396-401.
30. Espersen F, Clemmensen I. Isolation of a fibronectin-binding protein from Staphylococcus aureus. Infect Immun 1982; 37:526-31.
31. Fröman G, Switalski LM, Speziale P, Höök M. Isolation and characterization of a fibronectin receptor from Staphylococcus aureus. J Biol Chem 1987;262:6564-71.
32. Flock J-I, Fröman G, Jönsson K, Guss B, Signäs C, Nilsson B, Raucci G, Höök M, Wadström T, Lindberg M. Clon-ing and expression of the gene for a fibronectin-binding protein from Staphylococcus aureus. EMBO J 1987;6: 2351-7.
33. Switalski LM, Ryden C, Rubin K, Ljungh Å, Höök M, Wadström T. Binding of fibronectin to Staphylococcus strains. Infect Immun 1983;42:628-33.
34. Proctor RA, Prendergast E, Mosher DF. Fibronectin mediates attachment of Staphylococcus aureus to human neutrophils. Blood 1982;59:681-7.
35. Kuusela P, Vartio T, Vuento M, Myhre EB. Attachment of staphylococci and streptococci on fibronectin, fibronectin fragments, and fibrinogen bound to a solid phase. Infect Immun 1985;50:77-81.
36. 125I-Fibrinogen uptake on peripheral venous cannulas: A comparison between different cannula materials and coatings. J Biomed Mater Res 1987; 21:99-105.
37. Horbett TA, Cheng CM, Ratner BD, Hoffman AS, Hanson SR. The kinetics of baboon fibrinogen adsorption to polymers: In vitro and in vivo studies. J Biomed Mater Res 1986;20:739-72.
38. Peters WR, Bush WH Jr, McIntyre RD, Hill LD. The development of fibrin sheath on indwelling venous catheters. Surg Gynecol Obstet 1973;137:43-7.
39. Welch GW, McKeel DW Jr, Silverstein P, Walker HL. The role of catheter composition in the development of thrombophlebitis. Surg Gynecol Obstr 1974;138:421-4.
40. Brismar B, Härdstedt C, Jacobson S. Diagnosis of throm bosis by catheter phlebography after prolonged central venous catheterization, Ann Surg 1981;194:779-83.
41. Stillman RM, Soliman F, Garcia L, Sawyer PN. Etiology of catheter-associated sepsis. Correlation with thiombogenic-ity. Arch Surg 1977;112:1497-9.
42. Ratcliffe FM. Suppurative thrombosis of the superior venacava: A lethal complication of central venous catheters. Intensive Care Med 1985;11:265-6.
43. Doolittle RF. Fibrinogen and fibrin. Annu Rev Biochem 1984;53:195-229.
44. Allington MJ. Fibrinogen and fibrin degradation products and the clumping of staphylococci by serum. Br J Hae-matol 1967;13:550-67.
45. Usui Y. Biochemical properties of fibrinogen binding protein (clumping factor) of the staphylococcal cell surface. Zentralbl Bakteriol Mikrobiol Hyg [A] 1986;262:289-97.
46. Toy PTCY, Lai L-W, Drake TA, Sande MA. Effect of fibronec-tin on adherence of Staphylococcus aureus to fibrin thrombi in vitro. Infect Immun 1985;48:83-6.
47. Leammler C, de Freitas JC, Chhatwal GS, Blobel H. Interactions of immunoglobulin F, fibrinogen and fibronectin with Staphylococcus hyicus and Staphylococcus inter-medius. Zentralbl Bakteriol Mikrobiol Hyg [A] 1985;260:232-7.
48. Timpl R, Rohde H, Robey PG, Rennard SI, Foidart J-M, Martin GR. Laminin-a glycoprotein of basement membranes. J Biol Chem 1979;254:9933-7.
49. Terranova VP, DiFlorio R, Hujanen ES, Lyall RM, Liotta LA, Thorgeirsson U, Siegal GP, Schiffmann E. Laminin promotes rabbit neutrophil motility and attachment. J Clin Invest 1986;77:1180-6.
50. Nakatsuji N. Presumptive mesoderm cells from Xenopuslaevis gastrulae attach to and migrate on substrata coated with fibronectin or laminin. J Cell Sci 1986;86:109-18.
51. Perri RT, Vercellotti G, McCarthy J, Vessella RL, Furcht LT. Laminin selectively enhances monocyte-macrophage-mediated tumoricidal activity. J Lab Clin Med 1985;105:30-5.
52. Gressner AM, Tittor W, Negwer A, Pick-Kober K-H. Serum concentrations of laminin and aminoterminal propeptide of type III procollagen in relation to the portal venous pressure of fibrotic liver diseases. Clin Chim Acta 1986;161: 249-58.
53. Peters G, Schumacher-Perdreau F, Jansen B, Bey M, Pulverer G. Biology of S. epidermidis extracellular slime. In: Pul-verer G, Quie PG, Peters G, eds. Pathogenicity and clinical significance of coagulase-negative staphylococci. Stuttgart, FRG: Gustav Fischer Verlag, 1987:15-32.
54. Ludwicka A, Uhlenbruck G, Peters G, Seng PN, Gray ED, Jeljaszewicz J, Pulverer G. Investigation on extracellular slime substance produced by staphylococcus epidermidis. Zentralbl Bakteriol Mikrobiol Hyg [A] 1984;258:256-67.
55. Costerton JW, Irvin RT, Cheng K-J. The bacterial glycoca-lyx in nature and disease. Annu Rev Microbiol 1981;35: 299-324.
56. Geesey GG. Microbial exopolymers: Ecological and economic considerations. American Society for Microbiology Newsletter 1982;48:9-14.
57. Peters G, Saborowski F, Locci R. Pulverer G. Investigations on staphylococcal infection of transvenous endocardial pacemaker electrodes. Am Heart J 1984;108:359-65.
58. Kristinsson KG, Spencer RC, Brown CB. Clinical importance of production of slime by coagulase negative staphylococci in chronic ambulatory peritoneal dialysis. J Clin Pathol 1986;39:117-8.
59. Davenport DS, Massanari RM, Pfaller MA, Bale MJ, Streed SA, Hierholzer WJ Jr. Usefulness of a test for slime production as a marker for clinically significant infections with coagulase-negative staphylococci. J Infect Dis 1986;153: 332-9.
60. Christensen GD, Simpson WA, Bisno AL, Beachey EH. Experimental foreign body infections in mice challenged with slime-producing Staphylococcus epidermidis. Infect Immun 1983;40:407-10.
61. Ishak MA, Gróschel DHM, Mandell GL, Wenzel RP. Association of slime with pathogenicity of coagulase-negative staphylococci causing nosocomial septicemia. J Clin Microbiol 1985;22:1025-9.
62. Diaz-Mitoma F, Harding GKM, Hoban DJ, Roberts RS, Low DE. Clinical significance of a test for slime production in ventriculoperitoneal shunt infections caused by coagulase-negative staphylococci. J Infect Dis 1987; 156:555-60.
63. Younger JJ, Christensen GD, Bartley DL, Simmons JCH, Barrett FF. Coagulase-negative staphylococci isolated from cerebrospinal fluid shunts: Importance of slime production, species identification, and shunt removal to clinical outcome. J Infect Dis 1987;156:548-54.