Abstract
The formation of vegetations consisting of fibrin, cellular elements, humoral factors, and bacteria is the central event in the pathogenesis of bacterial endocarditis. Fibrin formation occurs on the vegetation, the coagulation system being activated locally via the expression of tissue factor (TF) on fibrin-adherent monocytes. This study was performed to assess the importance of phagocytosis of fibrin-adherent Streptococcus sanguis in the stimulation of TF expression on fibrin-adherent monocytes, as well as a role for "frustrated" phagocytosis. With the latter process, these cells are unable to remove bacteria from the fibrin surface but nonetheless might be activated to generate TF. We found that serum was not required for the stimulation of TF expression by fibrin-adherent monocytes in the presence of S. sanguis in an in vitro model for bacterial endocarditis. The bacterial adhesin dextran did not influence the TF activity (TFA) of fibrin-adherent monocytes: TFA was the same after stimulation with a dextran-positive streptococcus as with its dextran-negative mutant. Furthermore, dextran did not influence the TFA of endocardial vegetations, which was the same for vegetations isolated from rabbits infected either with dextran-positive S. sanguis or its dextran-negative mutant. These results do not support the hypothesis that in bacterial endocarditis (frustrated) phagocytosis significantly contributes to TF expression on vegetation-adherent monocytes. Fibronectin, however, although not influencing the fibrin binding of the streptococci, did enhance the TFA of monocytes in a concentration-dependent manner. We conclude that although streptococci do enhance expression of TFA on monocytes, phagocytosis and bacterial adhesins do not play a major role in this process. Stimulation of monocyte TFA may be more dependent on interactions between monocytes and the vegetational surface via fibronectin receptors, such as VLA 4 and VLA 5 (very late antigens 4 and 5).
Full Text
The Full Text of this article is available as a PDF (243.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bancsi M. J., Thompson J., Bertina R. M. Stimulation of monocyte tissue factor expression in an in vitro model of bacterial endocarditis. Infect Immun. 1994 Dec;62(12):5669–5672. doi: 10.1128/iai.62.12.5669-5672.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bancsi M. J., Veltrop M. H., Bertina R. M., Thompson J. Influence of monocytes and antibiotic treatment on tissue factor activity of endocardial vegetations in rabbits infected with Streptococcus sanguis. Infect Immun. 1996 Feb;64(2):448–451. doi: 10.1128/iai.64.2.448-451.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bom V. J., van Hinsbergh V. W., Reinalda-Poot H. H., Mohanlal R. W., Bertina R. M. Extrinsic activation of human coagulation factors IX and X on the endothelial surface. Thromb Haemost. 1991 Sep 2;66(3):283–291. [PubMed] [Google Scholar]
- Buiting A. G., Thompson J., Emeis J. J., Mattie H., Brommer E. J., van Furth R. Effects of tissue-type plasminogen activator (t-PA) on Streptococcus sanguis-infected endocardial vegetations in vitro. J Antimicrob Chemother. 1988 May;21(5):609–620. doi: 10.1093/jac/21.5.609. [DOI] [PubMed] [Google Scholar]
- Buiting A. G., Thompson J., van der Keur D., Schmal-Bauer W. C., Bertina R. M. Procoagulant activity of endocardial vegetations and blood monocytes in rabbits with Streptococcus sanguis endocarditis. Thromb Haemost. 1989 Nov 24;62(3):1029–1033. [PubMed] [Google Scholar]
- Böyum A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g. Scand J Clin Lab Invest Suppl. 1968;97:77–89. [PubMed] [Google Scholar]
- Durack D. T., Beeson P. B. Experimental bacterial endocarditis. I. Colonization of a sterile vegetation. Br J Exp Pathol. 1972 Feb;53(1):44–49. [PMC free article] [PubMed] [Google Scholar]
- Fan S. T., Mackman N., Cui M. Z., Edgington T. S. Integrin regulation of an inflammatory effector gene. Direct induction of the tissue factor promoter by engagement of beta 1 or alpha 4 integrin chains. J Immunol. 1995 Apr 1;154(7):3266–3274. [PubMed] [Google Scholar]
- Lowrance J. H., Baddour L. M., Simpson W. A. The role of fibronectin binding in the rat model of experimental endocarditis caused by Streptococcus sanguis. J Clin Invest. 1990 Jul;86(1):7–13. doi: 10.1172/JCI114717. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Manning J. E., Hume E. B., Hunter N., Knox K. W. An appraisal of the virulence factors associated with streptococcal endocarditis. J Med Microbiol. 1994 Feb;40(2):110–114. doi: 10.1099/00222615-40-2-110. [DOI] [PubMed] [Google Scholar]
- Meddens M. J., Thompson J., Leijh P. C., van Furth R. Role of granulocytes in the induction of an experimental endocarditis with a dextran-producing Streptococcus sanguis and its dextran-negative mutant. Br J Exp Pathol. 1984 Apr;65(2):257–265. [PMC free article] [PubMed] [Google Scholar]
- Meddens M. J., Thompson J., Mattie H., van Furth R. Role of granulocytes in the prevention and therapy of experimental Streptococcus sanguis endocarditis in rabbits. Antimicrob Agents Chemother. 1984 Feb;25(2):263–267. doi: 10.1128/aac.25.2.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scheld W. M., Valone J. A., Sande M. A. Bacterial adherence in the pathogenesis of endocarditis. Interaction of bacterial dextran, platelets, and fibrin. J Clin Invest. 1978 May;61(5):1394–1404. doi: 10.1172/JCI109057. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thörig L., Thompson J., Eulderink F., Emeis J. J., Van Furth R. Effects of monocytopenia and anticoagulation in experimental Streptococcus sanguis endocarditis. Br J Exp Pathol. 1980 Feb;61(1):108–116. [PMC free article] [PubMed] [Google Scholar]
- van Ginkel C. J., Thörig L., Thompson J., Oh J. I., van Aken W. G. Enhancement of generation of monocyte tissue thromboplastin by bacterial phagocytosis: possible pathway for fibrin formation on infected vegetations in bacterial endocarditis. Infect Immun. 1979 Jul;25(1):388–395. doi: 10.1128/iai.25.1.388-395.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Ginkel C. J., van Aken W. G., Oh J. I., Vreeken J. Stimulation of monocyte procoagulant activity by adherence to different surfaces. Br J Haematol. 1977 Sep;37(1):35–45. [PubMed] [Google Scholar]
- van der Meer J. W., van de Gevel J. S., Elzenga-Claassen I., van Furth R. Suspension cultures of mononuclear phagocytes in the teflon culture bag. Cell Immunol. 1979 Jan;42(1):208–212. doi: 10.1016/0008-8749(79)90236-3. [DOI] [PubMed] [Google Scholar]