Literature DB >> 6274803

Chemostat studies of the effect of environmental control on Streptococcus sanguis adherence to hydroxyapatite.

B Rosan, B Appelbaum, L K Campbell, K W Knox, A J Wicken.   

Abstract

Streptococcus sanguis is a major component of early dental plaque. The ability of S. sanguis to adhere to salivary pellicle appears to involve specific bacterial surface receptors. The nature of these receptors is still not known; however, the component molecules may be subject to environmental control as has been shown for teichoic acids and certain proteins. To study these environmental effects, a chemostat was employed to vary the growth conditions of Streptococcus sanguis strain G9B. This strain has been used extensively to study the adhesion of [(3)H]thymidine-labeled batch-grown cells to saliva-coated hydroxyapatite beads. The effects of dilution rate, pH, and carbon source on adhesion were studied with a competition assay in which the labeled batch cells were used as a reference standard. In this assay, cells from the chemostat were harvested and compared for their ability to inhibit adhesion of labeled cells relative to unlabeled control batch-grown cells. Subsequent studies used chemostat grown cells labeled with [(3)H]thymidine as a reference standard so that results were internally controlled and reflected only the particular alteration in environment which was studied. These results indicated that when glucose was used as a growth-limiting substrate, cells grown at relatively high dilution rates (D = 0.5 h(-1); mean generation time = 1.4 h) behaved similarly to batch-grown cells and appeared to compete for the same binding sites. Cells grown at D = 0.1 h(-1) (mean generation time = 7 h) no longer competed with either batch-grown cells or chemostat cells grown at D = 0.5 h(-1). Moreover, adsorption isotherms of such slow-growing cells (D = 0.1 h(-1)) suggested that binding was no longer specific. When fructose was used as the growth-limiting carbohydrate, cells grown at D = 0.1 h(-1) did not show this loss of specificity and competed nearly as well as control batch-grown glucose cells. However, the effect of pH appeared to be independent of carbohydrate source, because cells grown in either glucose or fructose at pH 5.5 at D = 0.1 h(-1) lost the ability to compete with reference batch or chemostat cells grown at D = 0.5 h(-1). This effect was very sharp, since cells grown in the pH range from 6 to 7.5 at D = 0.5 h(-1) competed nearly as well as control cells. A similar effect of pH was found for batch cultures grown with excess glucose. These studies reinforce the idea that the environment can profoundly affect the bacterial surface and consequently the ability of the organism to adhere, a property which appears to be a primary event in some infectious diseases and in dental plaque formation.

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Year:  1982        PMID: 6274803      PMCID: PMC350996          DOI: 10.1128/iai.35.1.64-70.1982

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  22 in total

1.  Lactobacilli and streptococci in the mouth of children.

Authors:  J Carlsson; H Grahnén; G Jonsson
Journal:  Caries Res       Date:  1975       Impact factor: 4.056

2.  Microbial population shifts in developing human dental plaque.

Authors:  H L Ritz
Journal:  Arch Oral Biol       Date:  1967-12       Impact factor: 2.633

3.  In vitro studies of dental plaque formation: adsorption of oral streptococci to hydroxyaptite.

Authors:  B Appelbaum; E Golub; S C Holt; B Rosan
Journal:  Infect Immun       Date:  1979-08       Impact factor: 3.441

4.  Effect of growth conditions on the formation of extracellular lipoteichoic acid by Streptococcus mutans BHT.

Authors:  N A Jacques; L Hardy; K W Knox; A J Wicken
Journal:  Infect Immun       Date:  1979-07       Impact factor: 3.441

5.  Mechanism of coaggregation between Actinomyces viscosus T14V and Streptococcus sanguis 34.

Authors:  F C McIntire; A E Vatter; J Baros; J Arnold
Journal:  Infect Immun       Date:  1978-09       Impact factor: 3.441

6.  Comparative estimates of bacterial affinities and adsorption sites on hydroxyapatite surfaces.

Authors:  W B Clark; L L Bammann; R J Gibbons
Journal:  Infect Immun       Date:  1978-03       Impact factor: 3.441

7.  Characterization of tufted streptococci isolated from the "corn cob" configuration of human dental plaque.

Authors:  C Mouton; H S Reynolds; R J Genco
Journal:  Infect Immun       Date:  1980-01       Impact factor: 3.441

8.  Effect of growth rate and glucose concentration on the biochemical properties of Streptococcus mutans Ingbritt in continuous culture.

Authors:  I R Hamilton; P J Phipps; D C Ellwood
Journal:  Infect Immun       Date:  1979-12       Impact factor: 3.441

9.  Effect of fructose and other carbohydrates on the surface properties, lipoteichoic acid production, and extracellular proteins of Streptococcus mutans Ingbritt grown in continuous culture.

Authors:  L Hardy; N A Jacques; H Forester; L K Campbell; K W Knox; A J Wicken
Journal:  Infect Immun       Date:  1981-01       Impact factor: 3.441

10.  Phosphoenolpyruvate-dependent sucrose phosphotransferase activity in Streptococcus mutans NCTC 10449.

Authors:  A M Slee; J M Tanzer
Journal:  Infect Immun       Date:  1979-06       Impact factor: 3.441

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  13 in total

1.  Comparative studies on the effect of growth conditions on adhesion, hydrophobicity, and extracellular protein profile of Streptococcus sanguis G9B.

Authors:  K W Knox; L N Hardy; L J Markevics; J D Evans; A J Wicken
Journal:  Infect Immun       Date:  1985-11       Impact factor: 3.441

2.  Influence of growth conditions on adherence of Streptococcus mutans ingbritt to saliva-coated hydroxyapatite.

Authors:  L K Campbell; K W Knox; A J Wicken
Journal:  Infect Immun       Date:  1983-01       Impact factor: 3.441

3.  Optimization of an hydroxyapatite adhesion assay for Streptococcus sanguis.

Authors:  R Eifert; B Rosan; E Golub
Journal:  Infect Immun       Date:  1984-05       Impact factor: 3.441

4.  Adherence of oral streptococci: evidence for nonspecific adsorption to saliva-coated hydroxylapatite surfaces.

Authors:  R H Staat; J C Peyton
Journal:  Infect Immun       Date:  1984-06       Impact factor: 3.441

5.  Aggregation of 27 oral bacteria by human whole saliva. Influence of culture medium, calcium, and bacterial cell concentration, and interference by autoaggregation.

Authors:  H M Koop; M Valentijn-Benz; A V Nieuw Amerongen; P A Roukema; J De Graaff
Journal:  Antonie Van Leeuwenhoek       Date:  1989-03       Impact factor: 2.271

6.  Bacteroides gingivalis-Actinomyces viscosus cohesive interactions as measured by a quantitative binding assay.

Authors:  S Schwarz; R P Ellen; D A Grove
Journal:  Infect Immun       Date:  1987-10       Impact factor: 3.441

7.  Preparation of a sialic acid-binding protein from Streptococcus mitis KS32AR.

Authors:  P A Murray; M J Levine; M S Reddy; L A Tabak; E J Bergey
Journal:  Infect Immun       Date:  1986-08       Impact factor: 3.441

8.  Streptococcus mutans fructosyltransferase (ftf) and glucosyltransferase (gtfBC) operon fusion strains in continuous culture.

Authors:  D L Wexler; M C Hudson; R A Burne
Journal:  Infect Immun       Date:  1993-04       Impact factor: 3.441

9.  Identification and characterization of a surface protein-releasing activity in Streptococcus mutans and other pathogenic streptococci.

Authors:  S F Lee
Journal:  Infect Immun       Date:  1992-10       Impact factor: 3.441

10.  Corncob formation between Fusobacterium nucleatum and Streptococcus sanguis.

Authors:  P Lancy; J M Dirienzo; B Appelbaum; B Rosan; S C Holt
Journal:  Infect Immun       Date:  1983-04       Impact factor: 3.441

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