Interbacterial binding among strains of pathogenic and commensal oral bacterial species

Oral Microbiology and Immunology

Volumn 11, Issue 1, 1996, Pages 35-41

  Yao, E S ^a   Lamont, R J ^a   Leu, S P ^a   Weinberg, A ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Bacteroides forsythus; Interbacterial adherence; Porphyromonas gingivalis; Streptococcus crista; Treponema denticola

Indexed keywords

EID: 0030088098     PISSN: 09020055     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-302X.1996.tb00334.x     Document Type: Article

References (37)

1. Cimasoni G, McBride BC. Adherence of Treponema denticola to modified hydroxyapatite. J Dent Res 1987: 66: 1727-1729.
2. Cockayne A, Sanger R, Ivic A et al. Antigenic and structural analysis of Treponema denticola. J Gen Microbiol 1989: 135: 3209-3218.
3. Gibbons RJ. Bacterial adhesion to oral tissues: a model for infectious diseases. J Dent Res 1989: 68: 750-760.
4. Gibbons RJ, van Houte J. On the formation of dental plaques. J Periodontol 1973: 44: 347-360.
5. Gouldbourne, PA, Ellen RP. Evidence that Porphyromonas (Bacteroides) gingivalis fimbriae function in adhesion to Actinomyces viscosus. J Bacteriol 1991: 173: 5266-5274.
6. Grenier D. Demonstration of a bimodal coagsregration reaction between Porphyromonas gingivalis and Treponema denticola. Oral Microbiol Immunol 1992: 7: 280-284.
7. Grenier D, Mayrand D. Nutritional relationships between oral bacteria. Infect Immun 1986: 53: 616-620.
8. Hasty DL, Ofek I, Courtney HS, Doyle RJ. Multiple adhesins of streptococci. Infect Immun 1992: 60: 2147-2152.
9. Inoshita E, Araano A, Hanioka T, Tamagawa H, Shizukuishi S, Tsunemitsu A. Isolation and some properties of exohemagglutinin from the culture medium of Bacteroides gingivalis 381. Infect Immun 1986: 52: 421-427.
10. Isogai H, Isogai E, Yoshimura F, Suzuki T, Kagota W, Takano K. Specific inhibition of adherence of an oral strain of Bacteroides gingivalis 381 to epithelial cells by monoclonal antibodies against the bacterial fimbriae. Arch Oral Biol 1988: 33: 479-485.
11. Kinder SA, Holt SC. Characterization of coaggregation between Bacteroides gingivalis T22 and Fusobacterium micleaium T18. Infect Immun 1989: 57: 3425-3433.
12. Kolenbrander PE, London J. Adhere today, here tomorrow: oral bacterial adherence. J Bacteriol 1993: 175: 3247-3252.
13. Lament RJ, Bevan CA, Gil S. Persson RE, Rosan B. Involvement of Porphyromonas gingivalis fimbriae in adherence to Streptococcus gordonii. Oral Microbiol Immunol 1993: 8: 272-276.
14. Lamont RJ. Gil S. Demuth DR, Malamud D, Rosan B. Molecules of Streptococcus gordonii that bind to Porphyromonas gingivalis. Microbiology 1994: 140: 867-872.
15. Lamont RJ, Hersey SG. Rosan B. Characterization of the adherence of Porphyromonas (Bacteroides) gingivalis to oral streptococci Oral Microbiol Immunol 1992: 7 193-197.
16. Lamont RJ. Hsiao GW. Gil S. Identification of a molecule of Porphyromonas gingivalis that binds to Streptococcus gordonii. Microb Pathog (in press).
17. Lamont RJ, Rosan B. Adherence of mutans streptococci to other other bacteria. Infect Immun 1990: 58: 1738-1743.
18. Lamont RJ, Rosan B, Baker CT. Nelson GM. Characterization of an adhesin antigen of Streptococcus sanguis G9B. Infect Immun 1988: 56: 2417-2473.
19. Lee J-Y. Sojar HT. Bedi GS, Genco RJ. Synthetic peptides analogous to the fimbrillin sequence inhibit adherence of Porphyromonas gingivalis. Infect Immun 1992: 60: 1662-1672.
20. Listgarten MA. Structure of the microbial flora associated with periodontal health and disease in man. J Periodontol 1976: 47: 1-18.
21. McBride BC, van der Hoeven JS. Role of interbacterial adherence in colonization of oral cavities of gnotobiotic rats infected with Streptococcus mutons and Veulonella alcalescens. Infect Immun 1981:33: 467-472.
22. Mouton C, Ni Eidhin D, Deslauriers M. Lamy L. The hemagglutinating adhesin HA-Ag2 of Bacteroides gingivalis is distinct from fimbrillin. Oral Microbiol Immunol 1991:6: 6-11.
23. Nagata H. Murakami Y. Inoshita E, Shizukuishi S, Tsunemitsu A. Inhibitory effect of human plasma and saliva on coaggregation between Bacteroides gingivalis and Streptococcus mitis. J Dent Res 1990: 69: 1476-1479.
24. Okuda K. Yamamoto A, Naito Y, Takazoe I. Slots J, Genco RJ. Purification and properties of hemagglutinin from culture supernatant of Bacteroides gingivalis Infect Immun 1986: 54: 659-665.
25. Progulske-Fox A. Tumwasorn S, Holt SC. The expression and function of a Bacteroides gingivalis hemagglutinin gene in Escherichia coli. Oral Microbiol Immunol 1989:4: 121-131.
26. Ritz HL, Microbial population shifts in developing human dental plaque. Arch Oral Biol 1967: 12: 1561-1568.
27. Scannapieco FA, Solomon L. Wadenya RO. Emergence in human dental plaque and host distribution of amylase-binding streptococci. J Dent Res 1994: 73: 1627-1635.
28. Slots J, Gibbons RJ. Attachment of Bacteroides melaninogenicus subsp. asaccharolyticus to oral surfaces and its possible role in the colonization of the mouth and of periodontal pockets. Infect Immun 1978: 19: 254-264.
29. Socransky SS. Haffajee AD. The bacterial etiology of destructive periodontal disease: current concepts. J Periodontol 1992: 63: 322-331.
30. Socransky SS. Manganiello AD, Propas D, Oram V, van Home J. Bacteriological studies of developing supragingival denial plaque, J Periodont Res 1977: 12: 90106.
31. Theilade E. Wright WH. Jensen SB, Löe H. Experimental gingivitis in man. II. A longitudinal clinical and bacteriological investigation. J Periodont RES 1966: 1: 113.
32. van der Hoeven JS, de Jong MH. Kolenbrander PE. In vivo studies of microbial adherence in dental plaque. In: Mergenhagen SE, Rosan B, ed. Molecular basis of oral microbial adhesion. Washington, DC: Am Soc Microbiol 1985: 220-227.
33. Watanabe K. Yamaji Y. Umemoto T. Correlation of cell-adherent activity and surface structure in Porphyromonas gingivalis. Oral Microbiol Immunol 1992: 7: 357-363.
34. Weinberg A. Holt SC. Chemical and biological activities of a 64-kilodalton outer sheath protein from Treponema demicola strains. J Bacteriol !991: 173: 6935-6947.
35. Wyatt JE, Willcox MPD, Russell RRB. Handley PS. Fibrillar strains of Streptococcus sanguis biotype 1 carry a surface protein which cross-reacts with antigen B from Streptococcus mutans Ingbritt. Oral Microbiol Immunol 1988: 3: 162-168.
36. Yoshimura F, Takahashi K, Nodasaka Y, Suzuki T. Purification and characterization of a novel type of fimbriae from the oral anaerobe Bacteroides gingivalis. J Bacteriol 1984: 160: 949-957.
37. Yotis WW. Macaluso F. Gopalsami C. Extraction of a lipopolysaccharide-like macromolecule (LPS) from Treponema denticola. J Dent Res 1994: 73 (spec issue): 156.