Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1976 Oct;14(4):1022–1027. doi: 10.1128/iai.14.4.1022-1027.1976

Initial colonization of teeth in monkeys as related to diet.

M Kilian, G Rölla
PMCID: PMC415488  PMID: 825462

Abstract

The initial phases of plaque development on nonretentive tooth surfaces were studied bacteriologically in Macaca irus monkeys fed by stomach tube and provided with various oral supplements. Except for the oral implantation of Streptococcus mutans in some of the animals, the oral flora was not changed prior to the studies. Dental plaque was allowed to develop on initially cleaned tooth surfaces for 3 to 5 h. Plaque samples were collected and cultured on a number of selective and nonselective agar media, and several hundred isolates from each sample were isolated and identified. The numerically predominant organisms in initial plaque were S. mutans, Streptococcus sanguis, and Actinomyces viscosus. Additional organisms regularly found, but usually in smaller numbers, were Streptococcus mitior and a group of fastidious gram-negative rods including Haemophilus species, Eikenella corrodens, and Actinobacillus actinomycetem-comitans. The colonization of S. mutans was dependent on sucrose and occurred at the expense of S. sanguis. In these experiments S. mutans accounted for 25 to 65% of the primary plaque formers. All other species encountered colonized the teeth irrespective of the diet. It is postulated that the early sucrose-dependent establishment of S. mutans directly on the enamel pellicle plays a key role in the development of a cariogenic plaque.

Full text

PDF
1022

Selected References

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

  1. Berkowitz R. J., Jordan H. V., White G. The early establishment of Streptococcus mutans in the mouths of infants. Arch Oral Biol. 1975 Mar;20(3):171–174. doi: 10.1016/0003-9969(75)90005-9. [DOI] [PubMed] [Google Scholar]
  2. Bowen W. H., Cornick D. E. The microbiology of gingival-dental plaque recent findings from primate research. Int Dent J. 1970 Sep;20(3):382–395. [PubMed] [Google Scholar]
  3. Bowen W. H. Effect of restricting oral intake to invert sugar or casein on the microbiology of plaque in Macaca fascicularis (irus). Arch Oral Biol. 1974 Mar;19(3):231–239. doi: 10.1016/0003-9969(74)90267-2. [DOI] [PubMed] [Google Scholar]
  4. Carlsson J., Grahnén H., Jonsson G., Wikner S. Establishment of Streptococcus sanguis in the mouths of infants. Arch Oral Biol. 1970 Dec;15(12):1143–1148. doi: 10.1016/0003-9969(70)90005-1. [DOI] [PubMed] [Google Scholar]
  5. Carlsson J. Presence of various types of non-haemolytic streptococci in dental plaque and in other sites of the oral cavity in man. Odontol Revy. 1967;18(1):55–74. [PubMed] [Google Scholar]
  6. Cornick D. E., Bowen W. H. The effect of sorbitol on the microbiology of the dental plaque in monkeys (Macaca irus). Arch Oral Biol. 1972 Dec;17(12):1637–1648. doi: 10.1016/0003-9969(72)90226-9. [DOI] [PubMed] [Google Scholar]
  7. Cross T., Goodfellow M. Taxonomy and classification of the actinomycetes. Soc Appl Bacteriol Symp Ser. 1973 Jan;2:11–112. [PubMed] [Google Scholar]
  8. De Stoppelaar J. D., Van Houte J., Backer DIRKS O. The effect of carbohydrate restriction on the presence of Streptococcus mutans, Streptococcus sanguis and iodophilic polysaccharide-producing bacteria in human dental plaque. Caries Res. 1970;4(2):114–123. doi: 10.1159/000259633. [DOI] [PubMed] [Google Scholar]
  9. Gibbons R. J., Depaola P. F., Spinell D. M., Skobe Z. Interdental localization of Streptococcus mutans as related to dental caries experience. Infect Immun. 1974 Mar;9(3):481–488. doi: 10.1128/iai.9.3.481-488.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gibbons R. J., Fitzgerald R. J. Dextran-induced agglutination of Streptococcus mutans, and its potential role in the formation of microbial dental plaques. J Bacteriol. 1969 May;98(2):341–346. doi: 10.1128/jb.98.2.341-346.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. 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]
  12. Gibbons R. J., Nygaard M. Interbacterial aggregation of plaque bacteria. Arch Oral Biol. 1970 Dec;15(12):1397–1400. doi: 10.1016/0003-9969(70)90031-2. [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. Gibbons R. J., van Houte J. On the formation of dental plaques. J Periodontol. 1973 Jun;44(6):347–360. doi: 10.1902/jop.1973.44.6.347. [DOI] [PubMed] [Google Scholar]
  15. Guggenheim B., Schroeder H. E. Biochemical and morphological aspects of extracellular polysaccharides produced by cariogenic streptococci. Helv Odontol Acta. 1967 Oct;11(2):131–152. [PubMed] [Google Scholar]
  16. HUGH R., LEIFSON E. The taxonomic significance of fermentative versus oxidative metabolism of carbohydrates by various gram negative bacteria. J Bacteriol. 1953 Jul;66(1):24–26. doi: 10.1128/jb.66.1.24-26.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hillman J. D., Van Houte J., Gibbons R. J. Sorption of bacteria to human enamel powder. Arch Oral Biol. 1970 Sep;15(9):899–903. doi: 10.1016/0003-9969(70)90163-9. [DOI] [PubMed] [Google Scholar]
  18. Jensen S. B., Löe H., Schiött C. R., Theliade E. Experimental gingivitis in man. 4. Vancomycin induced changes in bacterial plaque composition as related to development of gingival inflammation. J Periodontal Res. 1968;3(4):284–293. doi: 10.1111/j.1600-0765.1968.tb01934.x. [DOI] [PubMed] [Google Scholar]
  19. Jones S. J. A special relationship between spherical and filamentous microorganisms in mature human dental plaque. Arch Oral Biol. 1972 Mar;17(3):613–616. doi: 10.1016/0003-9969(72)90081-7. [DOI] [PubMed] [Google Scholar]
  20. Jordan H. V., Englander H. R., Engler W. O., Kulczyk S. Observations on the implantation and transmission of Streptococcus mutans in humans. J Dent Res. 1972 Mar-Apr;51(2):515–518. doi: 10.1177/00220345720510024501. [DOI] [PubMed] [Google Scholar]
  21. KRASSE B. THE EFFECT OF THE DIET ON THE IMPLANTATION OF CARIES-INDUCING STREPTOCOCCI IN HAMSTERS. Arch Oral Biol. 1965 Mar-Apr;10:215–221. doi: 10.1016/0003-9969(65)90022-1. [DOI] [PubMed] [Google Scholar]
  22. Kelstrup J., Funder-Nielsen T. D. Aggregation of oral streptococci with Fusobacterium and Actinomyces. J Biol Buccale. 1974 Dec;2(4):347–362. [PubMed] [Google Scholar]
  23. Kilian M. A taxonomic study of the genus Haemophilus, with the proposal of a new species. J Gen Microbiol. 1976 Mar;93(1):9–62. doi: 10.1099/00221287-93-1-9. [DOI] [PubMed] [Google Scholar]
  24. Kilian M., Schiott C. R. Haemophili and related bacteria in the human oral cavity. Arch Oral Biol. 1975 Dec;20(12):791–796. doi: 10.1016/0003-9969(75)90055-2. [DOI] [PubMed] [Google Scholar]
  25. Krasse B., Edwardsson S., Svensson I., Trell L. Implantation of caries-inducing streptococci in the human oral cavity. Arch Oral Biol. 1967 Feb;12(2):231–236. doi: 10.1016/0003-9969(67)90042-8. [DOI] [PubMed] [Google Scholar]
  26. Larmas M., Mäkinen K. K., Scheinin A. Turku sugar studies. III. An intermediate report on the effect of sucrose, fructose and xylitol diets on the numbers of salivary lactobacilli, candida and streptococci. Acta Odontol Scand. 1974;32(6):423–433. doi: 10.3109/00016357409026551. [DOI] [PubMed] [Google Scholar]
  27. Liljemark W. F., Gibbons R. J. Ability of Veillonella and Neisseria species to attach to oral surfaces and their proportions present indigenously. Infect Immun. 1971 Sep;4(3):264–268. doi: 10.1128/iai.4.3.264-268.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Liljemark W. F., Gibbons R. J. Proportional distribution and relative adherence of Streptococcus miteor (mitis) on various surfaces in the human oral cavity. Infect Immun. 1972 Nov;6(5):852–859. doi: 10.1128/iai.6.5.852-859.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Listgarten M. A., Mayo H. E., Tremblay R. Development of dental plaque on epoxy resin crowns in man. A light and electron microscopic study. J Periodontol. 1975 Jan;46(1):10–26. doi: 10.1902/jop.1975.46.1.10. [DOI] [PubMed] [Google Scholar]
  30. McBride B. C., Bourgeau G. Dextran-induced aggregation of Actinomyces viscosus. Arch Oral Biol. 1975 Dec;20(12):837–841. doi: 10.1016/0003-9969(75)90063-1. [DOI] [PubMed] [Google Scholar]
  31. Mikx F. H., Van Der Hoeven J. S., Plasschaert A. J., König K. G. Effect of Actinomyces viscosus on the establishment and symbiosis of Streptococcus mutans and Streptococcus sanguis in SPF rats on different sucrose diets. Caries Res. 1975;9(1):1–20. doi: 10.1159/000260138. [DOI] [PubMed] [Google Scholar]
  32. Mikx F. H., van der Hoeven J. S., Plasschaert A. J., König K. G. Establishment and symbiosis of Actinomyces viscosus, Streptococcus sanguis and Streptococcus mutans in germ-free Osborne-Mendel rats. Caries Res. 1976;10(2):123–132. doi: 10.1159/000260196. [DOI] [PubMed] [Google Scholar]
  33. Orstavik D., Kraus F. W., Henshaw L. C. In vitro attachment of streptococci to the tooth surface. Infect Immun. 1974 May;9(5):794–800. doi: 10.1128/iai.9.5.794-800.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Ritz H. L. Microbial population shifts in developing human dental plaque. Arch Oral Biol. 1967 Dec;12(12):1561–1568. doi: 10.1016/0003-9969(67)90190-2. [DOI] [PubMed] [Google Scholar]
  35. Saxton C. A. Scanning electron microscope study of the formation of dental plaque. Caries Res. 1973;7(2):102–119. doi: 10.1159/000259835. [DOI] [PubMed] [Google Scholar]
  36. Syed S. A., Loesche W. J., Pape H. L., Jr, grenier E. Predominant cultivable flora isolated from human root surface caries plaque. Infect Immun. 1975 Apr;11(4):727–731. doi: 10.1128/iai.11.4.727-731.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Theilade E., Wright W. H., Jensen S. B., Löe H. Experimental gingivitis in man. II. A longitudinal clinical and bacteriological investigation. J Periodontal Res. 1966;1:1–13. doi: 10.1111/j.1600-0765.1966.tb01842.x. [DOI] [PubMed] [Google Scholar]
  38. Van Houte J., Gibbons R. J., Banghart S. B. Adherence as a determinant of the presence of Streptococcus salivarius and Streptococcus sanguis on the human tooth surface. Arch Oral Biol. 1970 Nov;15(11):1025–1034. doi: 10.1016/0003-9969(70)90115-9. [DOI] [PubMed] [Google Scholar]
  39. Van Houte J., Green D. B. Relationship between the concentration of bacteria in saliva and the colonization of teeth in humans. Infect Immun. 1974 Apr;9(4):624–630. doi: 10.1128/iai.9.4.624-630.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES