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. 1977 Apr;16(1):203–212. doi: 10.1128/iai.16.1.203-212.1977

Decreased oral colonization of Streptococcus mutans during aging of Sprague-Dawley rats.

J Van Houte, V N Upeslacis, S Edelstein
PMCID: PMC421509  PMID: 873607

Abstract

The colonization by streptomycin-resistant Streptococcus mutans strains of the teeth of conventional and ex-germfree Sprague-Dawley rats of various ages fed either a high-sucrose or a high-glucose diet was studied. Bacterial colonization occurred with increasingly greater difficulty as the rats became older. This was observed in studies of the implantation of the test organism after oral inoculation with different cell numbers as well as its transmission between infected and uninfected rats. With rat fed sucrose diet, the effect of age could not be demonstrated until they were age 3 months or older; the results from rats fed a glucose diet suggest that changes may already have occurred early after weaning. Changes in susceptibility to colonization during aging manifested themselves as a decrease in the proportions of rats which became infected as well as lower population levels in infected rats. The possible mechanism(s) involved as well as the possible significance of the findings was discussed.

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Selected References

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  1. Aasenden R., Peebles T. C. Effects of fluoride supplementation from birth on human deciduous and permanent teeth. Arch Oral Biol. 1974 Apr;19(4):321–326. doi: 10.1016/0003-9969(74)90194-0. [DOI] [PubMed] [Google Scholar]
  2. BAILIT H. L., BALDWIN D. C., HUNT E. E., Jr THE INCREASING PREVALENCE OF GINGIVAL BACTEROIDES MELANINOGENICUS WITH AGE IN CHILDREN. Arch Oral Biol. 1964 Jul-Aug;9:435–438. doi: 10.1016/0003-9969(64)90028-7. [DOI] [PubMed] [Google Scholar]
  3. Bowen W. H. Dental caries in monkeys. Adv Oral Biol. 1968;3:185–216. doi: 10.1016/b978-1-4832-3119-8.50013-5. [DOI] [PubMed] [Google Scholar]
  4. Cheng H. C., Johnson D. C. Serum estrogens and gonadotropins in developing androgenized and normal female rats. Neuroendocrinology. 1974;13(6):357–365. doi: 10.1159/000122221. [DOI] [PubMed] [Google Scholar]
  5. Curbelo H. M., Houssay A. B., Gamper C. H., Kofoed J. A., Tocci A. A. Effects of oestrogens upon the sialic acid in the submaxillary and sublingual glands in the rat. Arch Oral Biol. 1974 Jun;19(6):421–423. doi: 10.1016/0003-9969(74)90146-0. [DOI] [PubMed] [Google Scholar]
  6. DE ARAUJO W. C., MACDONALD J. B. THE GINGIVAL CREVICE MICROBIOTA IN FIVE PRESCHOOL CHILDREN. Arch Oral Biol. 1964 Mar-Apr;9:227–228. doi: 10.1016/0003-9969(64)90013-5. [DOI] [PubMed] [Google Scholar]
  7. Döhler K. D., Wuttke W. Serum LH, FSH, prolactin and progesterone from birth to puberty in female and male rats. Endocrinology. 1974 Apr;94(4):1003–1008. doi: 10.1210/endo-94-4-1003. [DOI] [PubMed] [Google Scholar]
  8. Ebersole J. L., Molinari J. A., Platt D. Sequential appearance of salivary antibodies after oral immunization of axenic mice. Infect Immun. 1975 Aug;12(2):353–359. doi: 10.1128/iai.12.2.353-359.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FITZGERALD R. J., KEYES P. H. Ecologic factors in dental caries. The fate of antibiotic-resistant cariogenic streptococci in hamsters. Am J Pathol. 1963 Jun;42:759–772. [PMC free article] [PubMed] [Google Scholar]
  10. Fitzgerald D. B., Fitzgerald R. J. Plaque acid production in hamsters pretreated with fluoride. J Dent Res. 1973 Jan-Feb;52(1):111–115. doi: 10.1177/00220345730520010101. [DOI] [PubMed] [Google Scholar]
  11. GIBBONS R. J., SOCRANSKY S. S., KAPSIMALIS B. ESTABLISHMENT OF HUMAN INDIGENOUS BACTERIA IN GERM-FREE MICE. J Bacteriol. 1964 Nov;88:1316–1323. doi: 10.1128/jb.88.5.1316-1323.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gibbons R. J., Houte J. V. Bacterial adherence in oral microbial ecology. Annu Rev Microbiol. 1975;29:19–44. doi: 10.1146/annurev.mi.29.100175.000315. [DOI] [PubMed] [Google Scholar]
  13. Gibbons R. J., van Houte J. Dental caries. Annu Rev Med. 1975;26:121–136. doi: 10.1146/annurev.me.26.020175.001005. [DOI] [PubMed] [Google Scholar]
  14. Gold O. G., Jordan H. V., Van Houte J. A selective medium for Streptococcus mutans. Arch Oral Biol. 1973 Nov;18(11):1357–1364. doi: 10.1016/0003-9969(73)90109-x. [DOI] [PubMed] [Google Scholar]
  15. Gold O. G., Jordan H. V., van Houte J. The prevalence of enterococci in the human mouth and their pathogenicity in animal models. Arch Oral Biol. 1975 Jul;20(7):473–477. doi: 10.1016/0003-9969(75)90236-8. [DOI] [PubMed] [Google Scholar]
  16. Guggenheim B., König K. G., Mühlemann H. R. Modifications of the oral bacterial flora and their influence on dental caries in the rat. I. The effects of inoculating 4 labelled strains of streptococci. Helv Odontol Acta. 1965 Oct;9(2):121–129. [PubMed] [Google Scholar]
  17. KEYES P. H., FITZGERALD R. J. Dental caries in the Syrian hamster. IX. Arch Oral Biol. 1962 May-Jun;7:267–277. doi: 10.1016/0003-9969(62)90017-1. [DOI] [PubMed] [Google Scholar]
  18. Kalberer P. U., Schroeder H. E., Guggenheim B., Mühlemann H. R. The microbial colonization in fissures. A morphological and morphometric study in rat molars. Helv Odontol Acta. 1971 Apr;15(1):1–14. [PubMed] [Google Scholar]
  19. Kelstrup J. The incidence of bacteroides melaniogenicus in human gingival sulci, and its prevalence in the oral cavity at different ages. Periodontics. 1966 Jan-Feb;4(1):14–18. [PubMed] [Google Scholar]
  20. Liu F. T. Influence of some steroid contraceptives on icidence of dental caries and changes in salivary glands in female rats. J Dent Res. 1968 Nov-Dec;47(6):1047–1055. doi: 10.1177/00220345680470060801. [DOI] [PubMed] [Google Scholar]
  21. Magnusson I., Ericson T., Hugoson A. The effect of oral contraceptives on the concentration of some salivary substances in women. Arch Oral Biol. 1975 Feb;20(2):119–126. doi: 10.1016/0003-9969(75)90165-x. [DOI] [PubMed] [Google Scholar]
  22. SHAFER W. G., MUHLER J. C. Endocrine influences upon the salivary glands. Ann N Y Acad Sci. 1960 Mar 29;85:215–227. doi: 10.1111/j.1749-6632.1960.tb49960.x. [DOI] [PubMed] [Google Scholar]
  23. Van Houte J., Upeslacis V. N., Jordan H. V., Skobe Z., Green D. B. Role of sucrose in colonization of Streptococcus mutans in conventional Sprague-Dawley rats. J Dent Res. 1976 Mar-Apr;55(2):202–215. doi: 10.1177/00220345760550020801. [DOI] [PubMed] [Google Scholar]
  24. Van Houte J., Upeslacis V. N. Studies of the mechanism of sucrose-associated colonization of Streptococcus mutans on teeth of conventional rats. J Dent Res. 1976 Mar-Apr;55(2):216–222. doi: 10.1177/00220345760550020901. [DOI] [PubMed] [Google Scholar]
  25. van Houte J., Burgess R. C., Onose H. Oral implantation of human strains of Streptococcus mutans in rats fed sucrose or glucose diets. Arch Oral Biol. 1976;21(9):561–564. doi: 10.1016/0003-9969(76)90023-6. [DOI] [PubMed] [Google Scholar]

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