Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1988 Sep;56(9):2392–2399. doi: 10.1128/iai.56.9.2392-2399.1988

Natural occurrence of black-pigmented Bacteroides species in the gingival crevice of the squirrel monkey.

W B Clark 1, I Magnusson 1, C Abee 1, B Collins 1, J E Beem 1, W P McArthur 1
PMCID: PMC259578  PMID: 3410543

Abstract

The objective of this study was to determine whether the squirrel monkey (Saimiri scuireus) is indigenously colonized with black-pigmented bacteroides (BPB) resembling human Bacteroides gingivalis and Bacteroides intermedius (suspected periodontal pathogens) and to determine the usefulness of the squirrel monkey as an in vivo model for studying colonization by putative pathogens. We assayed the subgingival plaques of 138 monkeys of various ages and in four different colonies for the presence of anaerobic BPB microorganisms. We also tested half the animals for the presence of Actinobacillus actinomycetemcomitans. Clinical indices and levels of serum antibody to B. gingivalis were recorded. We detected BPB in 50% of the animals and A. actinomycetemcomitans in 69% of the animals. The presence of BPB was generally associated with increased age, increased gingival index, presence of calculus, and increased levels of serum antibody. These data indicate that the squirrel monkey may be a good model for studying the parameters of natural infection of the gingival crevice with suspected periodontopathogenic BPB microorganisms.

Full text

PDF
2392

Selected References

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

  1. Adams R. A., Zander H. A., Polson A. M. Interproximal and buccal cell populations apical to the sulcus before and during experimental periodontitis in squirrel monkeys. J Periodontol. 1981 Aug;52(8):416–419. doi: 10.1902/jop.1981.52.8.416. [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. Ebersole J. L., Frey D. E., Taubman M. A., Smith D. J. An ELISA for measuring serum antibodies to Actinobacillus actinomycetemcomitans. J Periodontal Res. 1980 Nov;15(6):621–632. doi: 10.1111/j.1600-0765.1980.tb00321.x. [DOI] [PubMed] [Google Scholar]
  4. Engvall E., Perlmann P. Enzyme-linked immunosorbent assay, Elisa. 3. Quantitation of specific antibodies by enzyme-labeled anti-immunoglobulin in antigen-coated tubes. J Immunol. 1972 Jul;109(1):129–135. [PubMed] [Google Scholar]
  5. Hausmann E., Ortman L. F., Sedransk N. Experimental alveolar bone loss in the monkey evaluated by 125I absorptiometry. Calcif Tissue Int. 1979 Nov 26;29(2):133–139. doi: 10.1007/BF02408068. [DOI] [PubMed] [Google Scholar]
  6. Heijl L., Rifkin B. R., Zander H. A. Conversion of chronic gingivitis to periodontitis in squirrel monkeys. J Periodontol. 1976 Dec;47(12):710–716. doi: 10.1902/jop.1976.47.12.710. [DOI] [PubMed] [Google Scholar]
  7. Kennedy J. E., Polson A. M. Experimental marginal periodontitis in squirrel monkeys. J Periodontol. 1973 Mar;44(3):140–144. doi: 10.1902/jop.1973.44.3.140. [DOI] [PubMed] [Google Scholar]
  8. Kiel R. A., Kornman K. S., Robertson P. B. Clinical and microbiological effects of localized ligature-induced periodontitis on non-ligated sites in the cynomolgus monkey. J Periodontal Res. 1983 Mar;18(2):200–211. doi: 10.1111/j.1600-0765.1983.tb00353.x. [DOI] [PubMed] [Google Scholar]
  9. Kornman K. S., Caffesse R. G., Nasjleti C. E. The effect of intensive antibacterial therapy on the sulcular environment in monkeys. Part I. Changes in the bacteriology of the gingival sulcus. J Periodontol. 1980 Jan;51(1):34–38. doi: 10.1902/jop.1980.51.1.34. [DOI] [PubMed] [Google Scholar]
  10. Kornman K. S., Holt S. C., Robertson P. B. The microbiology of ligature-induced periodontitis in the cynomolgus monkey. J Periodontal Res. 1981 Jul;16(4):363–371. doi: 10.1111/j.1600-0765.1981.tb00987.x. [DOI] [PubMed] [Google Scholar]
  11. Krygier G., Genco R. J., Mashimo P. A., Hausmann E. Experimental gingivitis in Macaca speciosa monkeys: clinical, bacteriologic and histologic similarities to human gingivitis. J Periodontol. 1973 Aug;44(8):454–463. doi: 10.1902/jop.1973.44.8.454. [DOI] [PubMed] [Google Scholar]
  12. LOE H., SILNESS J. PERIODONTAL DISEASE IN PREGNANCY. I. PREVALENCE AND SEVERITY. Acta Odontol Scand. 1963 Dec;21:533–551. doi: 10.3109/00016356309011240. [DOI] [PubMed] [Google Scholar]
  13. Leggott P. J., Anderson A. W., Punwani I., Sabet T., Murphy R., Crawford J. Phase contrast microscopy of microbial aggregates in the gingival sulcus of Macaca mulatta. Subgingival plaque bacteria in macaca mulatta. J Clin Periodontol. 1983 Jul;10(4):412–421. doi: 10.1111/j.1600-051x.1983.tb01290.x. [DOI] [PubMed] [Google Scholar]
  14. Mansheim B. J., Kasper D. L. Purification and immunochemical characterization of the outer membrane complex of Bacteroides melaninogenicus subspecies asaccharolyticus. J Infect Dis. 1977 May;135(5):787–799. doi: 10.1093/infdis/135.5.787. [DOI] [PubMed] [Google Scholar]
  15. Mansheim B. J., Stenstrom M. L., Low S. B., Clark W. B. Measurement of serum and salivary antibodies to the oral pathogen Bacteroides asaccharolyticus in human subjects. Arch Oral Biol. 1980;25(8-9):553–557. doi: 10.1016/0003-9969(80)90067-9. [DOI] [PubMed] [Google Scholar]
  16. Mashimo P. A., Ellison S. A., Slots J. Microbial composition of monkey dental plaque (Macaca arctoides and Macaca fascicularis). Scand J Dent Res. 1979 Feb;87(1):24–31. doi: 10.1111/j.1600-0722.1979.tb01936.x. [DOI] [PubMed] [Google Scholar]
  17. McArthur W. P., Stroup S., Wilson L. Detection and serotyping of Actinobacillus actinomycetemcomitans isolates on nitrocellulose paper blots with monoclonal antibodies. J Clin Periodontol. 1986 Aug;13(7):684–691. doi: 10.1111/j.1600-051x.1986.tb00866.x. [DOI] [PubMed] [Google Scholar]
  18. Mouton C., Hammond P. G., Slots J., Genco R. J. Serum antibodies to oral Bacteroides asaccharolyticus (Bacteroides gingivalis): relationship to age and periondontal disease. Infect Immun. 1981 Jan;31(1):182–192. doi: 10.1128/iai.31.1.182-192.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nalbandian J., Brecx M. C., Ooya K., Kornman K. S., Robertson P. B. Morphological studies on periodontal disease in the cynomolgus monkey. I. Light microscopic observations on gingivitis. J Periodontal Res. 1985 Mar;20(2):154–164. doi: 10.1111/j.1600-0765.1985.tb00422.x. [DOI] [PubMed] [Google Scholar]
  20. Rifkin B. R., Heijl L. The occurrence of mononuclear cells at sites of osteoclastic bone resorption in experimental periodontitis. J Periodontol. 1979 Dec;50(12):636–640. doi: 10.1902/jop.1979.50.12.636. [DOI] [PubMed] [Google Scholar]
  21. Slots J., Hausmann E. Longitudinal study of experimentally induced periodontal disease in Macaca arctoides: relationship between microflora and alveolar bone loss. Infect Immun. 1979 Feb;23(2):260–269. doi: 10.1128/iai.23.2.260-269.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Slots J. Selective medium for isolation of Actinobacillus actinomycetemcomitans. J Clin Microbiol. 1982 Apr;15(4):606–609. doi: 10.1128/jcm.15.4.606-609.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Slots J. Subgingival microflora and periodontal disease. J Clin Periodontol. 1979 Oct;6(5):351–382. doi: 10.1111/j.1600-051x.1979.tb01935.x. [DOI] [PubMed] [Google Scholar]
  24. Staple P. H., Reed M. J., Mashimo P. A., Sedransk N., Umemoto T. Diphenylhydantoin gingival hyperplasia in Macaca arctoides: prevention by inhibition of dental plaque deposition. J Periodontol. 1978 Jun;49(6):310–325. doi: 10.1902/jop.1978.49.6.310. [DOI] [PubMed] [Google Scholar]
  25. Taichman N. S., Shenker B. J., Tsai C. C., Glickman L. T., Baehni P. C., Stevens R., Hammond B. F. Cytopathic effects of Actinobacillus actinomycetemcomitans on monkey blood leukocytes. J Periodontal Res. 1984 Mar;19(2):133–145. doi: 10.1111/j.1600-0765.1984.tb00802.x. [DOI] [PubMed] [Google Scholar]
  26. Tanner A. C., Haffer C., Bratthall G. T., Visconti R. A., Socransky S. S. A study of the bacteria associated with advancing periodontitis in man. J Clin Periodontol. 1979 Oct;6(5):278–307. doi: 10.1111/j.1600-051x.1979.tb01931.x. [DOI] [PubMed] [Google Scholar]
  27. Tsai C. C., McArthur W. P., Baehni P. C., Hammond B. F., Taichman N. S. Extraction and partial characterization of a leukotoxin from a plaque-derived Gram-negative microorganism. Infect Immun. 1979 Jul;25(1):427–439. doi: 10.1128/iai.25.1.427-439.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. White D., Mayrand D. Association of oral Bacteroides with gingivitis and adult periodontitis. J Periodontal Res. 1981 May;16(3):259–265. doi: 10.1111/j.1600-0765.1981.tb00974.x. [DOI] [PubMed] [Google Scholar]
  29. Zambon J. J., Slots J., Genco R. J. Serology of oral Actinobacillus actinomycetemcomitans and serotype distribution in human periodontal disease. Infect Immun. 1983 Jul;41(1):19–27. doi: 10.1128/iai.41.1.19-27.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Zylber L. J., Jordan H. V. Development of a selective medium for detection and enumeration of Actinomyces viscosus and Actinomyces naeslundii in dental plaque. J Clin Microbiol. 1982 Feb;15(2):253–259. doi: 10.1128/jcm.15.2.253-259.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES