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. 1990 Dec;56(12):3890–3894. doi: 10.1128/aem.56.12.3890-3894.1990

Intrageneric coaggregation among strains of human oral bacteria: potential role in primary colonization of the tooth surface.

P E Kolenbrander 1, R N Andersen 1, L V Moore 1
PMCID: PMC185088  PMID: 2082831

Abstract

Of the 122 human oral bacterial strains tested from 11 genera, only streptococci and a few actinomyces exhibited coaggregation among the strains within their respective genera. Eight of the ten streptococci showed multiple intrageneric coaggregations, all of which were inhibited by galactosides. The widespread intrageneric coaggregation among the streptococci and the less extensive coaggregation among the actinomyces offers an explanation for their accretion on cleaned tooth surfaces and their dominance as primary colonizers.

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Selected References

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  1. Celesk R. A., London J. Attachment of oral Cytophaga species to hydroxyapatite-containing surfaces. Infect Immun. 1980 Aug;29(2):768–777. doi: 10.1128/iai.29.2.768-777.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ciardi J. E., McCray G. F., Kolenbrander P. E., Lau A. Cell-to-cell interaction of Streptococcus sanguis and Propionibacterium acnes on saliva-coated hydroxyapatite. Infect Immun. 1987 Jun;55(6):1441–1446. doi: 10.1128/iai.55.6.1441-1446.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cisar J. O., Kolenbrander P. E., McIntire F. C. Specificity of coaggregation reactions between human oral streptococci and strains of Actinomyces viscosus or Actinomyces naeslundii. Infect Immun. 1979 Jun;24(3):742–752. doi: 10.1128/iai.24.3.742-752.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. Cowan M. M., Taylor K. G., Doyle R. J. Energetics of the initial phase of adhesion of Streptococcus sanguis to hydroxylapatite. J Bacteriol. 1987 Jul;169(7):2995–3000. doi: 10.1128/jb.169.7.2995-3000.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gibbons R. J., Hay D. I., Cisar J. O., Clark W. B. Adsorbed salivary proline-rich protein 1 and statherin: receptors for type 1 fimbriae of Actinomyces viscosus T14V-J1 on apatitic surfaces. Infect Immun. 1988 Nov;56(11):2990–2993. doi: 10.1128/iai.56.11.2990-2993.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hughes C. V., Kolenbrander P. E., Andersen R. N., Moore L. V. Coaggregation properties of human oral Veillonella spp.: relationship to colonization site and oral ecology. Appl Environ Microbiol. 1988 Aug;54(8):1957–1963. doi: 10.1128/aem.54.8.1957-1963.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Johnson J. L., Moore L. V., Kaneko B., Moore W. E. Actinomyces georgiae sp. nov., Actinomyces gerencseriae sp. nov., designation of two genospecies of Actinomyces naeslundii, and inclusion of A. naeslundii serotypes II and III and Actinomyces viscosus serotype II in A. naeslundii genospecies 2. Int J Syst Bacteriol. 1990 Jul;40(3):273–286. doi: 10.1099/00207713-40-3-273. [DOI] [PubMed] [Google Scholar]
  9. Kolenbrander P. E., Andersen R. N. Characterization of Streptococcus gordonii (S. sanguis) PK488 adhesin-mediated coaggregation with Actinomyces naeslundii PK606. Infect Immun. 1990 Sep;58(9):3064–3072. doi: 10.1128/iai.58.9.3064-3072.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kolenbrander P. E., Andersen R. N., Holdeman L. V. Coaggregation of oral Bacteroides species with other bacteria: central role in coaggregation bridges and competitions. Infect Immun. 1985 Jun;48(3):741–746. doi: 10.1128/iai.48.3.741-746.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kolenbrander P. E., Andersen R. N. Inhibition of coaggregation between Fusobacterium nucleatum and Porphyromonas (Bacteroides) gingivalis by lactose and related sugars. Infect Immun. 1989 Oct;57(10):3204–3209. doi: 10.1128/iai.57.10.3204-3209.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kolenbrander P. E., Andersen R. N., Moore L. V. Coaggregation of Fusobacterium nucleatum, Selenomonas flueggei, Selenomonas infelix, Selenomonas noxia, and Selenomonas sputigena with strains from 11 genera of oral bacteria. Infect Immun. 1989 Oct;57(10):3194–3203. doi: 10.1128/iai.57.10.3194-3203.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kolenbrander P. E., Andersen R. N. Multigeneric aggregations among oral bacteria: a network of independent cell-to-cell interactions. J Bacteriol. 1986 Nov;168(2):851–859. doi: 10.1128/jb.168.2.851-859.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kolenbrander P. E., Celesk R. A. Coaggregation of human oral Cytophaga species and Actinomyces israelii. Infect Immun. 1983 Jun;40(3):1178–1185. doi: 10.1128/iai.40.3.1178-1185.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kolenbrander P. E., Inouye Y., Holdeman L. V. New Actinomyces and Streptococcus coaggregation groups among human oral isolates from the same site. Infect Immun. 1983 Aug;41(2):501–506. doi: 10.1128/iai.41.2.501-506.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kolenbrander P. E. Intergeneric coaggregation among human oral bacteria and ecology of dental plaque. Annu Rev Microbiol. 1988;42:627–656. doi: 10.1146/annurev.mi.42.100188.003211. [DOI] [PubMed] [Google Scholar]
  17. Kolenbrander P. E., Phucas C. S. Effect of saliva on coaggregation of oral Actinomyces and Streptococcus species. Infect Immun. 1984 May;44(2):228–233. doi: 10.1128/iai.44.2.228-233.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kolenbrander P. E. Surface recognition among oral bacteria: multigeneric coaggregations and their mediators. Crit Rev Microbiol. 1989;17(2):137–159. doi: 10.3109/10408418909105746. [DOI] [PubMed] [Google Scholar]
  19. Kolenbrander P. E., Williams B. L. Lactose-reversible coaggregation between oral actinomycetes and Streptococcus sanguis. Infect Immun. 1981 Jul;33(1):95–102. doi: 10.1128/iai.33.1.95-102.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kolenbrander P. E., Williams B. L. Prevalence of viridans streptococci exhibiting lactose-inhibitable coaggregation with oral actinomycetes. Infect Immun. 1983 Aug;41(2):449–452. doi: 10.1128/iai.41.2.449-452.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Lamont R. J., Rosan B., Murphy G. M., Baker C. T. Streptococcus sanguis surface antigens and their interactions with saliva. Infect Immun. 1988 Jan;56(1):64–70. doi: 10.1128/iai.56.1.64-70.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Morris E. J., McBride B. C. Adherence of Streptococcus sanguis to saliva-coated hydroxyapatite: evidence for two binding sites. Infect Immun. 1984 Feb;43(2):656–663. doi: 10.1128/iai.43.2.656-663.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nyvad B., Kilian M. Microbiology of the early colonization of human enamel and root surfaces in vivo. Scand J Dent Res. 1987 Oct;95(5):369–380. doi: 10.1111/j.1600-0722.1987.tb01627.x. [DOI] [PubMed] [Google Scholar]
  24. Shah H. N., Collins D. M. Prevotella, a new genus to include Bacteroides melaninogenicus and related species formerly classified in the genus Bacteroides. Int J Syst Bacteriol. 1990 Apr;40(2):205–208. doi: 10.1099/00207713-40-2-205. [DOI] [PubMed] [Google Scholar]
  25. Socransky S. S., Manganiello A. D., Propas D., Oram V., van Houte J. Bacteriological studies of developing supragingival dental plaque. J Periodontal Res. 1977 Mar;12(2):90–106. doi: 10.1111/j.1600-0765.1977.tb00112.x. [DOI] [PubMed] [Google Scholar]
  26. Syed S. A., Loesche W. J. Bacteriology of human experimental gingivitis: effect of plaque age. Infect Immun. 1978 Sep;21(3):821–829. doi: 10.1128/iai.21.3.821-829.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Weiss E. I., London J., Kolenbrander P. E., Kagermeier A. S., Andersen R. N. Characterization of lectinlike surface components on Capnocytophaga ochracea ATCC 33596 that mediate coaggregation with gram-positive oral bacteria. Infect Immun. 1987 May;55(5):1198–1202. doi: 10.1128/iai.55.5.1198-1202.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]

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