Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1996 Aug;64(8):3069–3073. doi: 10.1128/iai.64.8.3069-3073.1996

Experimental immunization of rats with a Streptococcus mutans 59-kilodalton glucan-binding protein protects against dental caries.

D J Smith 1, M A Taubman 1
PMCID: PMC174189  PMID: 8757835

Abstract

Glucan-binding proteins (GBPs) are theoretically important in the molecular pathogenesis of dental caries caused by Streptococcus mutans. The present study evaluated the ability of antibody induced by the S. mutans 59-kDa GBP (GBP59) to affect dental caries caused by experimental infection with S. mutans in a rodent model. Groups of 20-day-old rats were injected twice at 9-day intervals subcutaneously in the salivary gland vicinity with GBP59, glucosyltransferase (GTF), or phosphate-buffered saline (sham injection), each incorporated in an adjuvant. Two weeks after the second injection, GBP59- and GTF-injected rats contained significant levels of salivary immunoglobulin A and serum immunoglobulin G antibody to the respective injected antigens. However, cross-reacting antibody to S. mutans GTF or GBP59 was not induced by the respective antigen. Rats were then orally infected with S. mutans. After 71 days of infection, GBP59- and GTF-injected groups had smaller numbers of S. mutans on their molar surfaces, compared with the sham-injected infected group. Total, sulcal, and smooth-surface molar caries in the GBP59- and GTF-immunized S. mutans-infected groups were each significantly lower (P < or = 0.003) than the respective measures of caries in the sham injected infected group. The results of this investigation demonstrate that immunization with S. mutans GBP59 induces an immune response in rats that can interfere with the accumulation of S. mutans and can reduce the level of dental caries caused by this cariogenic streptococcus. Furthermore, the protective immunity induced by either GBP59 or GTF appears to result from antibodies to independent epitopes since these two S. mutans components do not have a close antigenic relationship.

Full Text

The Full Text of this article is available as a PDF (241.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abo H., Matsumura T., Kodama T., Ohta H., Fukui K., Kato K., Kagawa H. Peptide sequences for sucrose splitting and glucan binding within Streptococcus sobrinus glucosyltransferase (water-insoluble glucan synthetase). J Bacteriol. 1991 Feb;173(3):989–996. doi: 10.1128/jb.173.3.989-996.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Aduse-Opoku J., Gilpin M. L., Russell R. R. Genetic and antigenic comparison of Streptococcus mutans fructosyltransferase and glucan-binding protein. FEMS Microbiol Lett. 1989 Jun;50(3):279–282. doi: 10.1016/0378-1097(89)90432-1. [DOI] [PubMed] [Google Scholar]
  3. Aoki H., Shiroza T., Hayakawa M., Sato S., Kuramitsu H. K. Cloning of a Streptococcus mutans glucosyltransferase gene coding for insoluble glucan synthesis. Infect Immun. 1986 Sep;53(3):587–594. doi: 10.1128/iai.53.3.587-594.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Banas J. A., Russell R. R., Ferretti J. J. Sequence analysis of the gene for the glucan-binding protein of Streptococcus mutans Ingbritt. Infect Immun. 1990 Mar;58(3):667–673. doi: 10.1128/iai.58.3.667-673.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hanada N., Kuramitsu H. K. Isolation and characterization of the Streptococcus mutans gtfC gene, coding for synthesis of both soluble and insoluble glucans. Infect Immun. 1988 Aug;56(8):1999–2005. doi: 10.1128/iai.56.8.1999-2005.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hanada N., Kuramitsu H. K. Isolation and characterization of the Streptococcus mutans gtfD gene, coding for primer-dependent soluble glucan synthesis. Infect Immun. 1989 Jul;57(7):2079–2085. doi: 10.1128/iai.57.7.2079-2085.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Loesche W. J. Role of Streptococcus mutans in human dental decay. Microbiol Rev. 1986 Dec;50(4):353–380. doi: 10.1128/mr.50.4.353-380.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mooser G., Wong C. Isolation of a glucan-binding domain of glucosyltransferase (1,6-alpha-glucan synthase) from Streptococcus sobrinus. Infect Immun. 1988 Apr;56(4):880–884. doi: 10.1128/iai.56.4.880-884.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Russell R. R. Glucan-binding proteins of Streptococcus mutans serotype c. J Gen Microbiol. 1979 May;112(1):197–201. doi: 10.1099/00221287-112-1-197. [DOI] [PubMed] [Google Scholar]
  10. Russell R. R., Shiroza T., Kuramitsu H. K., Ferretti J. J. Homology of glucosyltransferase gene and protein sequences from Streptococcus sobrinus and Streptococcus mutans. J Dent Res. 1988 Mar;67(3):543–547. doi: 10.1177/00220345880670030401. [DOI] [PubMed] [Google Scholar]
  11. Smith D. J., Akita H., King W. F., Taubman M. A. Purification and antigenicity of a novel glucan-binding protein of Streptococcus mutans. Infect Immun. 1994 Jun;62(6):2545–2552. doi: 10.1128/iai.62.6.2545-2552.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Smith D. J., Taubman M. A. Development of salivary IgA antibody to oral streptococcal antigens associated with virulence. Adv Exp Med Biol. 1995;371B:1141–1143. [PubMed] [Google Scholar]
  13. Smith D. J., Taubman M. A., Holmberg C. F., Eastcott J., King W. F., Ali-Salaam P. Antigenicity and immunogenicity of a synthetic peptide derived from a glucan-binding domain of mutans streptococcal glucosyltransferase. Infect Immun. 1993 Jul;61(7):2899–2905. doi: 10.1128/iai.61.7.2899-2905.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Stack W. E., Taubman M. A., Tsukuda T., Smith D. J., Ebersole J. L., Kent R. Dental caries in congenitally athymic rats. Oral Microbiol Immunol. 1990 Dec;5(6):309–314. doi: 10.1111/j.1399-302x.1990.tb00431.x. [DOI] [PubMed] [Google Scholar]
  15. Talbman M. A., Smith D. J. Effects of local immunization with Streptococcus mutans on induction of salivary immunoglobulin A antibody and experimental dental caries in rats. Infect Immun. 1974 Jun;9(6):1079–1091. doi: 10.1128/iai.9.6.1079-1091.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Taubman M. A., Holmberg C. J., Smith D. J. Immunization of rats with synthetic peptide constructs from the glucan-binding or catalytic region of mutans streptococcal glucosyltransferase protects against dental caries. Infect Immun. 1995 Aug;63(8):3088–3093. doi: 10.1128/iai.63.8.3088-3093.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Taubman M. A., Smith D. J. Effects of local immunization with glucosyltransferase fractions from Streptococcus mutans on dental caries in rats and hamsters. J Immunol. 1977 Feb;118(2):710–720. [PubMed] [Google Scholar]
  18. Wong C., Hefta S. A., Paxton R. J., Shively J. E., Mooser G. Size and subdomain architecture of the glucan-binding domain of sucrose:3-alpha-D-glucosyltransferase from Streptococcus sobrinus. Infect Immun. 1990 Jul;58(7):2165–2170. doi: 10.1128/iai.58.7.2165-2170.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wren B. W. A family of clostridial and streptococcal ligand-binding proteins with conserved C-terminal repeat sequences. Mol Microbiol. 1991 Apr;5(4):797–803. doi: 10.1111/j.1365-2958.1991.tb00752.x. [DOI] [PubMed] [Google Scholar]
  20. Wren B. W., Russell R. R., Tabaqchali S. Antigenic cross-reactivity and functional inhibition by antibodies to Clostridium difficile toxin A, Streptococcus mutans glucan-binding protein, and a synthetic peptide. Infect Immun. 1991 Sep;59(9):3151–3155. doi: 10.1128/iai.59.9.3151-3155.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. von Eichel-Streiber C., Sauerborn M., Kuramitsu H. K. Evidence for a modular structure of the homologous repetitive C-terminal carbohydrate-binding sites of Clostridium difficile toxins and Streptococcus mutans glucosyltransferases. J Bacteriol. 1992 Oct;174(20):6707–6710. doi: 10.1128/jb.174.20.6707-6710.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES