Endocarditis-associated oral streptococci promote rapid differentiation of monocytes into mature dendritic cells

Infection and Immunity

Volumn 73, Issue 8, 2005, Pages 5015-5021

  Hahn, Chin Lo ^a   Schenkein, Harvey A ^a   Tew, John G ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD14 ANTIGEN; CD83 ANTIGEN; CD86 ANTIGEN; GLYCOPROTEIN P 15095; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; INTERLEUKIN 12; INTERLEUKIN 4; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2;

ALLOGENEIC RESTRICTION; ALPHA HEMOLYTIC STREPTOCOCCUS; ARTICLE; CELL DIFFERENTIATION; CELL POPULATION; DENDRITIC CELL; DISEASE ASSOCIATION; ENDOCARDITIS; HUMAN; HUMAN CELL; MIXED LYMPHOCYTE CULTURE; MONOCYTE; MOUTH FLORA; PATHOGENESIS; PHAGOCYTOSIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; STREPTOCOCCUS;

ANTIGENS, CD; ANTIGENS, CD11C; ANTIGENS, CD14; ANTIGENS, CD86; CELL DIFFERENTIATION; DENDRITIC CELLS; ENDOCARDITIS, BACTERIAL; HISTOCOMPATIBILITY ANTIGENS CLASS II; IMMUNOGLOBULINS; INTERLEUKIN-12; MEMBRANE GLYCOPROTEINS; MONOCYTES; MOUTH; PROTEIN SUBUNITS; STREPTOCOCCUS;

EID: 23344433123     PISSN: 00199567     EISSN: None     Source Type: Journal    
DOI: 10.1128/IAI.73.8.5015-5021.2005     Document Type: Article

References (40)

1. Bancsi, M. J., J. Thompson, and R. M. Bertina. 1994. Stimulation of monocyte tissue factor expression in an in vitro model of bacterial endocarditis. Infect. Immun. 62:5669-5672.
2. Bancsi, M. J., M. H. Veltrop, R. M. Bertina, and J. Thompson. 1996. Influence of monocytes and antibiotic treatment on tissue factor activity of endocardial vegetations in rabbits infected with Streptococcus sanguis. Infect. Immun. 64:448-451.
3. Bancsi, M. J., M. H. Veltrop, R. M. Bertina, and J. Thompson. 1996. Role of phagocytosis in activation of the coagulation system in Streptococcus sanguis endocarditis. Infect. Immun. 64:5166-5170.
4. Bayliss, R., C. Clarke, C. M. Oakley, W. Somerville, A. G. Whitfield, and S. E. Young. 1983. The microbiology and pathogenesis of infective endocarditis. Br. Heart J. 50:513-519.
5. Broussas, M., P. Cornillet-Lefebvre, J. Bernard, J. C. Adjizian, G. Potron, and P. Nguyen. 2000. Separation of dendritic cells from highly purified human monocytes by counterflow centrifugation induces tissue factor expression. Transfusion (Paris) 40:1088-1094.
6. Buiting, A. G., J. Thompson, D. van der Keur, W. C. Schmal-Bauer, and R. M. Bertina. 1989. Procoagulant activity of endocardial vegetations and blood monocytes in rabbits with Streptococcus sanguis endocarditis. Thromb. Haemost. 62:1029-1033.
7. Carrizosa, J., K. Kaye, and W. Kobasa. 1978. Experimental streptococcal endocarditis. The early vegetation. Arch. Pathol. Lab. Med. 102:518-521.
8. Cella, M., D. Scheidegger, K. Palmer-Lehmann, P. Lane, A. Lanzavecchia, and G. Alber. 1996. Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation. J. Exp. Med. 184:747-752.
9. Chia, J. S., Y. L. Lin, H. T. Lien, and J. Y. Chen. 2004. Platelet aggregation induced by serotype polysaccharides from Streptococcus mutans. Infect. Immun. 72:2605-2617.
10. Chomarat, P., J. Banchereau, J. Davoust, and A. K. Palucka. 2000. IL-6 switches the differentiation of monocytes from dendritic cells to macrophages. Nat. Immunol. 1:510-514.
11. Corinti, S., D. Medaglini, A. Cavani, M. Rescigno, G. Pozzi, P. Ricciardi-Castagnoli, and G. Girolomoni. 1999. Human dendritic cells very efficiently present a heterologous antigen expressed on the surface of recombinant gram-positive bacteria to CD4+ T lymphocytes. J. Immunol. 163:3029-3036.
12. Debelian, G. J., I. Olsen, and L. Tronstad. 1994. Systemic diseases caused by oral microorganisms. Endod. Dent. Traumatol. 10:57-65.
13. Durack, D. T., and P. B. Beeson. 1972. Experimental bacterial endocarditis. 11. Survival of a bacteria in endocardial vegetations. Br. J. Exp. Pathol. 53:50-53.
14. Hahn, C. L., A. M. Best, and J. G. Tew. 2000. Cytokine induction by Streptococcus mutans and pulpal pathogenesis. Infect. Immun. 68:6785-6789.
15. Harley, S. L., J. Sturge, and J. T. Powell. 2000. Regulation by fibrinogen and its products of intercellular adhesion molecule-1 expression in human saphenous vein endothelial cells. Arterioscler. Thromb. Vasc. Biol. 20:652-658.
16. Henneke, P., O. Takeuchi, R. Malley, E. Lien, R. R. Ingalls, M. W. Freeman, T. Mayadas, V. Nizet, S. Akira, D. L. Kasper, and D. T. Golenbock. 2002. Cellular activation, phagocytosis, and bactericidal activity against group B streptococcus involve parallel myeloid differentiation factor 88-dependent and -independent signaling pathways. J. Immunol. 169:3970-3977.
17. Herzberg, M. C. 1996. Platelet-streptococcal interactions in endocarditis. Crit. Rev. Oral Biol. Med. 7:222-236.
18. Holt, P. G., S. Haining, D. J. Nelson, and J. D. Sedgwick. 1994. Origin and steady-state turnover of class II MHC-bearing dendritic cells in the epithelium of the conducting airways. J. Immunol. 153:256-261.
19. Itoh, T., Y. Ueda, K. Okugawa, H. Fujiwara, N. Fuji, T. Yamashita, H. Fujiki, S. Harada, T. Yoshimura, and H. Yamagishi. 2003. Streptococcal preparation OK432 promotes functional maturation of human monocyte-derived dendritic cells. Cancer Immunol. Immunother. 52:207-214. (First published 25 February 2003; doi:10.1007/s00262-002-0337-8.)
20. Kamath, A. T., S. Henri, F. Battye, D. F. Tough, and K. Shortman. 2002. Developmental kinetics and lifespan of dendritic cells in mouse lymphoid organs. Blood 100:1734-1741.
21. Karlsson, H., P. Larsson, A. E. Wold, and A. Rudin. 2004. Pattern of cytokine responses to gram-positive and gram-negative commensal bacteria is profoundly changed when monocytes differentiate into dendritic cells. Infect. Immun. 72:2671-2678.
22. Kennedy, H. F., D. Morrison, D. Tomlinson, B. E. Gibson, J. Bagg, and C. G. Gemmell. 2003. Gingivitis and toothbrushes: potential roles in viridans streptococcal bacteraemia. J. Infect. 46:67-70.
23. Kikuchi, T., C. L. Hahn, S. Tanaka, S. E. Barbour, H. A. Schenkein, and J. G. Tew. 2004. Dendritic cells stimulated with Actinobacillus actinomycetemcomitans elicit rapid gamma interferon responses by natural killer cells. Infect. Immun. 72:5089-5096.
24. Kitten, T., C. L. Munro, S. M. Michalek, and F. L. Macrina. 2000. Genetic characterization of a Streptococcus mutans LraI family operon and role in virulence. Infect. Immun. 68:4441-4451.
25. Lien, E., T. J. Sellati, A. Yoshimura, T. H. Flo, G. Rawadi, R. W. Finberg, J. D. Carroll, T. Espevik, R. R. Ingalls, J. D. Radolf, and D. T. Golenbock. 1999. Toll-like receptor 2 functions as a pattern recognition receptor for diverse bacterial products. J. Biol. Chem. 274:33419-33425.
26. Munro, C. L., S. M. Michalek, and F. L. Macrina. 1995. Sucrose-derived exopolymers have site-dependent roles in Streptococcus mutans-promoted dental decay. FEMS Microbiol. Lett. 128:327-332.
27. Nakahara, S., T. Tsunoda, T. Baba, S. Asabe, and H. Tahara. 2003. Dendritic cells stimulated with a bacterial product, OK-432, efficiently induce cytotoxic T lymphocytes specific to tumor rejection peptide. Cancer Res. 63:4112-4118.
28. Nau, G. J., A. Schlesinger, J. F. Richmond, and R. A. Young. 2003. Cumulative Toll-like receptor activation in human macrophages treated with whole bacteria. J. Immunol. 170:5203-5209.
29. Pan, J., M. Zhang, J. Wang, Q. Wang, D. Xia, W. Sun, L. Zhang, H. Yu, Y. Liu, and X. Cao. 2004. Interferon-gamma is an autocrine mediator for dendritic cell maturation. Immunol. Lett. 94:141-151.
30. Regnault, A., D. Lankar, V. Lacabanne, A. Rodriguez, C. Thery, M. Rescigno, T. Saito, S. Verbeek, C. Bonnerot, P. Ricciardi-Castagnoli, and S. Amigorena. 1999. Fcgamma receptor-mediated induction of dendritic cell maturation and major histocompatibility complex class I-restricted antigen presentation after immune complex internalization. J. Exp. Med. 189:371-380.
31. Rogosa, M., E. G. Hampp, T. A. Nevin, H. N. Wagner, E. J. Driscoll, and P. N. Baer. 1960. Blood sampling and cultural studies in the detection of postoperative bacteremias. J. Am. Dent. Assoc. 60:171-180.
32. Thoma-Uszynski, S., S. M. Kiertscher, M. T. Ochoa, D. A. Bouis, M. V. Norgard, K. Miyake, P. J. Godowski, M. D. Roth, and R. L. Modlin. 2000. Activation of toll-like receptor 2 on human dendritic cells triggers induction of IL-12, but not IL-10. J. Immunol. 165:3804-3810.
33. Thorig, L., J. Thompson, F. Eulderink, J. J. Emeis, and R. Van Furth. 1980. Effects of monocytopenia and anticoagulation in experimental Streptococcus sanguis endocarditis. Br. J. Exp. Pathol. 61:108-116.
34. Uronen-Hansson, H., J. Allen, M. Osman, G. Squires, N. Klein, and R. E. Callard. 2004. Toll-like receptor 2 (TLR2) and TLR4 are present inside human dendritic cells, associated with microtubules and the Golgi apparatus but are not detectable on the cell surface: integrity of microtubules is required for interleukin-12 production in response to internalized bacteria. Immunology 111:173-178.
35. van de Rijn, I., M. George, A. Bouvet, and R. B. Roberts. 1986. Enzyme-linked immunosorbent assay for the detection of antibodies to nutritionally variant streptococci in patients with endocarditis. J. Infect. Dis. 153:116-121.
36. van der Meer, J. T., W. van Vianen, E. Hu, W. B. van Leeuwen, H. A. Valkenburg, J. Thompson, and M. F. Michel. 1991. Distribution, antibiotic susceptibility and tolerance of bacterial isolates in culture-positive cases of endocarditis in The Netherlands. Eur. J. Clin. Microbiol. Infect. Dis. 10:728-734.
37. Verhasselt, V., C. Buelens, F. Willems, D. De Greote, N. Haeffner-Cavaillon, and M. Goldman. 1997. Bacterial lipopolysaccharide stimulates the production of cytokines and the expression of costimulatory molecules by human peripheral blood dendritic cells: evidence for a soluble CD14-dependent pathway. J. Immunol. 158:2919-2925.
38. Visintin, A., A. Mazzoni, J. H. Spitzer, D. H. Wyllie, S. K. Dower, and D. M. Segal. 2001. Regulation of Toll-like receptors in human monocytes and dendritic cells. J. Immunol. 166:249-255.
39. Wallet, F., R. Dessein, S. Armand, and R. J. Courcol. 2002. Molecular diagnosis of endocarditis due to Lactobacillus casei subsp. rhamnosus. Clin. Infect. Dis. 35:e117-119. (First published 28 October 2002; doi:10.1086/344181).
40. Ze-Ze, L., R. Tenreiro, A. Duarte, M. J. Salgado, J. Melo-Cristino, L. Lito, M. M. Carmo, S. Felisberto, and G. Carmo. 2004. Case of aortic endocarditis caused by Lactobacillus casei. J. Med. Microbiol. 53:451-453.