Thromb Haemost 1987; 57(02): 222-225
DOI: 10.1055/s-0038-1651098
Original Article
Schattauer GmbH Stuttgart

Responses of Platelets to Strains of Streptococcus sanguis: Findings in Healthy Subjects, Bernard-Soulier, Glanzmann’s, and Collagen-Unresponsive Patients

A H Soberay
1   The School of Dentistry, University of Minnesota, Minneapolis, MN, USA
,
M C Herzberg
1   The School of Dentistry, University of Minnesota, Minneapolis, MN, USA
,
J D Rudney
1   The School of Dentistry, University of Minnesota, Minneapolis, MN, USA
,
H K Nieuwenhuis
2   The Department of Hematology, University Hospital Utrecht, The Netherlands
,
J J Sixma
2   The Department of Hematology, University Hospital Utrecht, The Netherlands
,
U Seligsohn
3   The Institute of Hematology, Ichilov Hospital, Tel Aviv, Israel
› Author Affiliations
Further Information

Publication History

Received 30 July 1986

Accepted after revision 29 January 1987

Publication Date:
28 June 2018 (online)

Summary

The ability of endocarditis and dental strains of Streptococcus sanguis to induce platelet aggregation in plasma (PRP) from normal subjects were examined and compared to responses of PRP with known platelet membrane glycoprotein (GP) and response defects.

S. sanguis strains differed in their ability to induce normal PRPs to aggregate. Strains that induced PRP aggregation in more than 60% of donors were significantly faster agonists (mean lag times to onset of aggregation less than 6 min) than those strains inducing response in PRPs of fewer than 60% of donors.

Platelets from patients with Bernard-Soulier syndrome aggregated in response to strains of S. sanguis. In contrast, platelets from patients with Glanzmann’s thrombasthenia and from a patient with a specific defect in response to collagen were unresponsive to S. sanguis. These observations show that GPIb and V are not essential, but GPIIb-IIIa and GPIa are important in the platelet response mechanism to S. sanguis. Indeed, the data suggests that the platelet interaction mechanisms of S. sanguis and collagen may be similar.

 
  • References

  • 1 Houlihan RB. Studies on the adhesion of human blood platelets and bacteria. Blood 1947; Special Issue No 1: 142-154
  • 2 Clawson CC, White JG. Platelet interaction with bacteria. I. Reaction phases and effects of inhibitors. Am J Pathol 1971; 65: 367-380
  • 3 Herzberg MC, Brintzenhofe K, Clawson CC. Aggregation of human platelets and adhesion of Streptococcus sanguis . Infect Immun 1983; 39: 1457-1469
  • 4 Hawiger J, Steckley S, Hammond D, Cheng C, Timmons S, Glick AA, DesPrez RM. Staphylococci-induced human platelet injury mediated by protein A and immunoglobulin G Fc receptor. J Clin Invest 1979; 64: 931-937
  • 5 Zimmerman TS, Spiegelberg HL. Pneumococcus-induced serotonin release from human platelets. J Clin Invest 1975; 56: 828-834
  • 6 Bick RL. Disseminated intravascular coagulation and related syndromes: etiology, pathophysiology, diagnosis, and managment. Am J Hematol 1978; 5: 265-282
  • 7 Clawson CC. The role of platelets in the pathogenesis of endocarditis. Am Heart Assoc Monogr 1979; 52: 24-27
  • 8 Herzberg MC, MacFarlane GD, Delzer PR. Streptococcus sanguis interactions with human platelets. In: Molecular Basis of Oral Microbial Adhesion. Mergenhagen SE, Rosan B. (eds.). p 53-60 Am Soc Microbiol; Washington, D.C.: 1985
  • 9 Sakariassen KS, Nievelstein P RE M, Coller BS, Sixma JJ. The role of platelet membrane glycoproteins Ib and IIb-IIIa in platelet adherence to human artery subendothelium. Br J Haematol 1986; 63: 681-691
  • 10 Bevers EM, Comfurius P, Levy-Toledano S, Enouf J, Nieuwenhuis HH, Caen JP, Qwaal R FA. Platelet prothrombin converting activity in hereditary disorders of platelet function. Br J Haematol 1986; 63: 335-345
  • 11 Seligsohn U, Rososhansky S. A Glanzmann’s thrombasthenia cluster among Iraqi Jews in Israel. Thromb Haemost 1984; 52: 230-231
  • 12 Nieuwenhuis HK, Akkerman J WN, Houdijk W PM, Sixma JJ. Human blood platelets showing no response to collagen fail to express surface glycoprotein Ia. Nature 1985; 318: 470-472
  • 13 Clawson CC, White JG, Herzberg MC. Platelet interaction with bacterial. VI. Contrasting the role of fibrinogen and fibronectin. Am J Hematol 1980; 9: 43-53
  • 14 Jenkins C SP, Meyer D, Dreyfus MD, Larrieu M. von Willebrand Factor and ristocetin. I. Mechanisms of ristocetin-induced platelet aggregation. Br J Haematol 1974; 28: 561-578
  • 15 Winer BJ. Statistical principles in experimental design. 2nd edition. p 261-309 McGraw-Hill; New York: 1971
  • 16 Dixon WJ. BMDP Statistical Software: 1983 Printing with Additions . p 359-387 University of California Press; Berkeley: 1983
  • 17 Sokal RR, Rohlf FJ. Biometry. 2nd edition. p 242-262 W. H. Freeman; San Francisco: 1981
  • 18 Shrout PE, Fleiss JL. Intraclass correlations: Uses in assessing rater reliability. Psychol Bull 1979; 86: 420-428
  • 19 Erickson PR, Herzberg MC. Purification of a platelet interactive antigen from Streptococcus sanguis . Submitted for publication
  • 20 Nieuwenhuis HK, Akkerman J WN, Sakariassen KS, Houdijk W PM, Nievelstein P FE M, Sixma JJ. Human blood platelets with a defect of response to collagen fail to express surface glycoprotein Ia. Thromb Haemost 1985; 54: 124 (Abstr. 0733)
  • 21 Nurden AT, Caen JP. The different glycoprotein abnormalities in Thrombasthenic and Bernard-Soulier platelets. Seminars in Hematol 1979; 16: 234-250
  • 22 Clemetson KJ, McGregor JL, James E, Dechavanne M, Lüscher EF. Characterization of the platelet membrane glycoprotein abnormalities in Bernard-Soulier syndrome and comparison with normal by surface labeling techniques and high resolution two-dimensional gel electrophoresis. J Clin Invest 1982; 70: 304-311
  • 23 Nurden AT, Caen JP. Specific roles for platelet surface glycoproteins in platelet function. Nature 1975; 255: 720-722
  • 24 George JN, Nurden AT, Phillips DR. Molecular defects in interactions of platelets with the vessel wall. N Eng J Med 1984; 311: 1084-1098
  • 25 Erickson PR, Herzberg MC. A collagen-like immunodeterminant on the surface of Streptococcus sanguisinduces platelet aggregation. J Immunol. 1987 (Accepted)
  • 26 Erickson PR, Herzberg MC. Plasma cofactors of Streptococcus sanguis induced platelet-aggregation. Submitted for publication
  • 27 Hawiger J, Kloczewiak M, Timmons S. Platelet-receptor mechanisms for adhesive macromolecules. In Interaction of Platelets with Vessel Wall. Oates JA, Hawiger J, Ross R. (eds.). pp. 1-19 Am Physiol Soc; Bethesda: 1985
  • 28 Coller BS. Activation affects access to the platelet receptor for adhesive glycoproteins. J Cell Biol 1986; 103: 451-456