Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1978 Dec;22(3):721–726. doi: 10.1128/iai.22.3.721-726.1978

Impaired colonization of gnotobiotic and conventional rats by streptomycin-resistant strains of Streptococcus mutans.

L L Bammann, W B Clark, R J Gibbons
PMCID: PMC422219  PMID: 730381

Abstract

Colonization of streptomycin-resistant mutants derived from Streptococcus mutans strain LB1, a human isolate, and strain FA-1, a rodent isolate, was studied in gnotobiotic and conventional rats. Mutants resistent to 2.0 mg of streptomycin per ml were isolated by using both stepwise (suffix "R"M) and one-step (suffix "R"1) selections. Rats were infected with mixtures of parental and streptomycin-resistant strains, and the proportions of each strain present in samples from the intestinal canal, tongue dorsum, teeth, and fissure plaque were determined. Combinations of strains investigated were LB1 and FA-1"R"M; FA-1 and LB1"R"M; LB1 and LB1"R"1; FA-1 and FA-1"R"1. In gnotobiotic rats, nonresistant strains predominated in every oral sample studied at 7 and 21 days after infection. Similarly, when conventional exgermfree rats were infected with FA-1 and FA-1"R"1, FA-1 dominated in all samples. Streptomycin-sensitive revertants were not detected in rats monoinfected with strains LB1"R"1 and FA-1"R"1 for 21 days. No antagonistic interactions were observed between the strains in in vitro experiments. Streptomycin-resistent mutants attached to hydroxyapatite treated with rat or human saliva in equal or higher numbers than did parental strains. However, parental strains appeared to grow faster in Trypticase soy broth then streptomycin-resistant mutants. These observations indicate that induction of streptomycin resistance frequently impairs the colonization properties of S. mutans strains, possibly by altering their rate of growth.

Full text

PDF
721

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. Similarity of bacteriocins of Streptococcus mutans from mother and infant. Arch Oral Biol. 1975 Nov;20(11):725–730. doi: 10.1016/0003-9969(75)90042-4. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Bowen W. H. The induction of rampant dental caries in monkeys (Macaca irus). Caries Res. 1969;3(3):227–237. doi: 10.1159/000259597. [DOI] [PubMed] [Google Scholar]
  4. Clark W. B., Bammann L. L., Gibbons R. J. Ability of Streptococcus mutans and a glucosyltransferase-defective mutant to colonize rodents and attach to hydroxyapatite surfaces. Infect Immun. 1978 Aug;21(2):681–684. doi: 10.1128/iai.21.2.681-684.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Clark W. B., Bammann L. L., Gibbons R. J. Comparative estimates of bacterial affinities and adsorption sites on hydroxyapatite surfaces. Infect Immun. 1978 Mar;19(3):846–853. doi: 10.1128/iai.19.3.846-853.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Clark W. B., Gibbons R. J. Influence of salivary components and extracellular polysaccharide synthesis from sucrose on the attachment of Streptococcus mutans 6715 to hydroxyapatite surfaces. Infect Immun. 1977 Nov;18(2):514–523. doi: 10.1128/iai.18.2.514-523.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Edman D. C., Keene H. J., Shklair I. L., Hoerman K. C. Dental floss for implantation and sampling of Streptococcus mutans from approximal surfaces of human teeth. Arch Oral Biol. 1975 Feb;20(2):145–148. doi: 10.1016/0003-9969(75)90171-5. [DOI] [PubMed] [Google Scholar]
  8. Evans R. T., Emmings F. G., Genco R. J. Prevention of Streptococcus mutans infection of tooth surfaces by salivary antibody in Irus monkeys (Macaca fascicularis). Infect Immun. 1975 Aug;12(2):293–302. doi: 10.1128/iai.12.2.293-302.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FITZGERALD R. J., JORDAN H. V., STANLEY H. R. Experimental caries and gingival pathologic changes in the gnotobiotic rat. J Dent Res. 1960 Sep-Oct;39:923–935. doi: 10.1177/00220345600390052701. [DOI] [PubMed] [Google Scholar]
  10. FITZGERALD R. J., KEYES P. H. Demonstration of the etiologic role of streptococci in experimental caries in the hamster. J Am Dent Assoc. 1960 Jul;61:9–19. doi: 10.14219/jada.archive.1960.0138. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. Gibbons R. J., Spinell D. M., Skobe Z. Selective adherence as a determinant of the host tropisms of certain indigenous and pathogenic bacteria. Infect Immun. 1976 Jan;13(1):238–246. doi: 10.1128/iai.13.1.238-246.1976. [DOI] [PMC free article] [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. 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]
  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. KEYES P. H., JORDAN H. V. PERIODONTAL LESIONS IN THE SYRIAN HAMSTER. III. FINDINGS RELATED TO AN INFECTIOUS AND TRANSMISSIBLE COMPONENT. Arch Oral Biol. 1964 Jul-Aug;9:377–400. doi: 10.1016/0003-9969(64)90024-x. [DOI] [PubMed] [Google Scholar]
  19. Kelstrup J., Gibbons R. J. Bacteriocins from human and rodent streptococci. Arch Oral Biol. 1969 Mar;14(3):251–258. doi: 10.1016/0003-9969(69)90227-1. [DOI] [PubMed] [Google Scholar]
  20. 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]
  21. Krasse B., Jordan H. V. Effect of orally applied vaccines on oral colonization by Streptococcus mutans in rodents. Arch Oral Biol. 1977;22(8-9):479–484. doi: 10.1016/0003-9969(77)90041-3. [DOI] [PubMed] [Google Scholar]
  22. McGhee, Michalek S. M., Webb J., Navia J. M., Rahman A. F., Legler D. W. Effective immunity to dental caries: protection of gnotobiotic rats by local immunization with Streptococcus mutans. J Immunol. 1975 Jan;114(1 Pt 2):300–305. [PubMed] [Google Scholar]
  23. Michalek S. M., McGhee J. R., Mestecky J., Arnold R. R., Bozzo L. Ingestion of Streptococcus mutans induces secretory immunoglobulin A and caries immunity. Science. 1976 Jun 18;192(4245):1238–1240. doi: 10.1126/science.1273589. [DOI] [PubMed] [Google Scholar]
  24. Pine L., Reeves M. W. Correlation of M protein production with those factors found to influence growth and substrate utilization of Streptococcus pyogenes. Infect Immun. 1972 May;5(5):668–680. doi: 10.1128/iai.5.5.668-680.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Shockman G. D. Symposium on the fine structure and replication of bacteria and their parts. IV. Unbalanced cell-wall synthesis: autolysis and cell-wall thickening. Bacteriol Rev. 1965 Sep;29(3):345–358. doi: 10.1128/br.29.3.345-358.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Svanberg M. L., Loesche W. J. Implantation of Streptococcus mutans on tooth surfaces in man. Arch Oral Biol. 1978;23(7):551–556. doi: 10.1016/0003-9969(78)90269-8. [DOI] [PubMed] [Google Scholar]
  27. 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]
  28. 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]
  29. Van Houte J., Gibbons R. J., Pulkkinen A. J. Adherence as an ecological determinant for streptococci in the human mouth. Arch Oral Biol. 1971 Oct;16(10):1131–1141. doi: 10.1016/0003-9969(71)90042-2. [DOI] [PubMed] [Google Scholar]
  30. Van Houte J., Upeslacis V. N., Edelstein S. Decreased oral colonization of Streptococcus mutans during aging of Sprague-Dawley rats. Infect Immun. 1977 Apr;16(1):203–212. doi: 10.1128/iai.16.1.203-212.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. 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]
  32. 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]
  33. van Houte J., Saxton C. A. Cell wall thickening and intracellular polysaccharide in microorganisms of the dental plaque. Caries Res. 1971;5(1):30–43. doi: 10.1159/000259730. [DOI] [PubMed] [Google Scholar]

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

RESOURCES