Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1975 Sep;12(3):576–585. doi: 10.1128/iai.12.3.576-585.1975

Model system for studying colonization and growth of bacteria on a hydroxyapatite surface.

S Z Sudo, J R Gutfleisch, N K Schotzko, L E Folke
PMCID: PMC415326  PMID: 1100524

Abstract

A model system for the study of bacterial colonization and growth on a hydroxyapatite (HT) surface is described. Hydroxyapatite was crystallized over the surface of porous glass beads. Chemical analysis of the product showed that the ratio of Ca2+/P042- was indistinguishable from that of commercial HT powder. X-ray diffraction analysis supported the conclusion that the product was HT. A system employing [14C]polyethylene glycol, which selectively adsorbs to the glass surface of the beads, was developed to determine the amount of glass surface covered by HT. Over 90% of the glass surface could be covered by our method. The product, HT beads, consisted of approximately 20% (dry weight) HT. The HT beads possess several properties which make them potentially useful for studying microbial adherence, growth, and interactions. These include: (i) chemical similarity to the tooth surface, (ii) large surface area, and (iii) high density. We also describe a method for direct measurement of the microbial mass of cells growing on beads. The method entails immobilizing a sample on a membrane filter (Millipore), staining it with amido black dye, and eluting the dye for spectrophotometric measurement. Streptococcus mutans served as the test organism. For free-growing bacteria the values measured with the filter assay were directly proportional to cell number, with a value of 1 mug of "protein" corresponding to about 1.5 X 10(6) colony-forming units, determined by viable count. For bacteria colonizing the beads, 1 mug of protein corresponded to about 2 X 10(7) colony-forming units on the beads during logarithmic growth. As the culture approached stationary phase, the efficiency of the assay decreased. These data indicate that multiple random samples, taken at a given time, are representative of the entire culture.

Full text

PDF
576

Images in this article

Selected References

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

  1. Hay D. I., Gibbons R. J., Spinell D. M. Characteristics of some high molecular weight constituents with bacterial aggregating activity from whole saliva and dental plaque. Caries Res. 1971;5(2):111–123. doi: 10.1159/000259739. [DOI] [PubMed] [Google Scholar]
  2. Hay D. I. The interaction of human parotid salivary proteins with hydroxyapatite. Arch Oral Biol. 1973 Dec;18(12):1517–1529. doi: 10.1016/0003-9969(73)90127-1. [DOI] [PubMed] [Google Scholar]
  3. Hay D. I. The isolation from human parotid saliva of a tyrosine-rich acidic peptide which exhibits high affinity for hydroxyapatite surfaces. Arch Oral Biol. 1973 Dec;18(12):1531–1541. doi: 10.1016/0003-9969(73)90128-3. [DOI] [PubMed] [Google Scholar]
  4. 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]
  5. Jordan H. V., Keyes P. H. In vitro methods for the study of plaque formation and carious lesions. Arch Oral Biol. 1966 Aug;11(8):793–802. doi: 10.1016/0003-9969(66)90005-7. [DOI] [PubMed] [Google Scholar]
  6. Kaitila I. The mechanism by which tetracycline hydrochloride inhibits mineralization in vitro. Biochim Biophys Acta. 1971 Sep 21;244(3):584–594. doi: 10.1016/0304-4165(71)90075-4. [DOI] [PubMed] [Google Scholar]
  7. Kashket S., Donaldson C. G. Saliva-induced aggregation of oral streptococci. J Bacteriol. 1972 Dec;112(3):1127–1133. doi: 10.1128/jb.112.3.1127-1133.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. McCabe R. M., Keyes P. H., Howell A., Jr An in vitro method for assessing the plaque forming ability of oral bacteria. Arch Oral Biol. 1967 Dec;12(12):1653–1656. doi: 10.1016/0003-9969(67)90200-2. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Miller C. H. Degradation of sucrose by whole cells and plaque of Actinomyces naeslundii. Infect Immun. 1974 Dec;10(6):1280–1291. doi: 10.1128/iai.10.6.1280-1291.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Miller C. H., Kleinman J. L. Effect of microbial interactions on in vitro plaque formation by Streptococcus mutans. J Dent Res. 1974 Mar-Apr;53(2):427–434. doi: 10.1177/00220345740530024201. [DOI] [PubMed] [Google Scholar]
  12. Mukasa H., Slade H. D. Mechanism of adherence of Streptococcus mutans to smooth surfaces. I. Roles of insoluble dextran-levan synthetase enzymes and cell wall polysaccharide antigen in plaque formation. Infect Immun. 1973 Oct;8(4):555–562. doi: 10.1128/iai.8.4.555-562.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Olson G. A., Bleiweis A. S., Small P. A., Jr Adherence inhibition of Streptococcus mutans: an assay reflecting a possible role of antibody in dental caries prophylaxis. Infect Immun. 1972 Apr;5(4):419–427. doi: 10.1128/iai.5.4.419-427.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Parsons J. C., Jr, Miller C. H. Plaque formation by mixed cultures of nonprimary plaque-forming microorganisms. J Dent Res. 1974 Jul-Aug;53(4):825–831. doi: 10.1177/00220345740530041001. [DOI] [PubMed] [Google Scholar]
  15. Schaffner W., Weissmann C. A rapid, sensitive, and specific method for the determination of protein in dilute solution. Anal Biochem. 1973 Dec;56(2):502–514. doi: 10.1016/0003-2697(73)90217-0. [DOI] [PubMed] [Google Scholar]
  16. Sumner J. B. A METHOD FOR THE COLORIMETRIC DETERMINATION OF PHOSPHORUS. Science. 1944 Nov 3;100(2601):413–414. doi: 10.1126/science.100.2601.413. [DOI] [PubMed] [Google Scholar]
  17. Tanzer J. M., McCabe R. M. Selection of plaque-forming streptococci by the serial passage of wires through sucrose-containing broth. Arch Oral Biol. 1968 Jan;13(1):139–143. doi: 10.1016/0003-9969(68)90045-9. [DOI] [PubMed] [Google Scholar]
  18. Tanzer J. M., Reid Y., Reid W. Method for preclinical evaluation of antiplaque agents. Antimicrob Agents Chemother. 1972 May;1(5):376–380. doi: 10.1128/aac.1.5.376. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. de Stoppelaar J. D., König K. G., Plasschaert A. J., van der Hoeven J. S. Decreased cariogenicity of a mutant of Streptococcus mutans. Arch Oral Biol. 1971 Aug;16(8):971–975. doi: 10.1016/0003-9969(71)90186-5. [DOI] [PubMed] [Google Scholar]

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

RESOURCES