Literature DB >> 3198842

Utilization of a continuous streptococcal surface to measure interbacterial adherence in vitro and in vivo.

W F Liljemark1, C G Bloomquist, M C Coulter, L J Fenner, R J Skopek, C F Schachtele.   

Abstract

Cell-to-cell interactions are essential for the formation of dental plaque. A continuous layer of Streptococcus sanguis SA-1 cells fixed to a solid surface has been used to evaluate interactions among this bacterium, Haemophilus parainfluenzae, and Streptococcus sobrinus. S. sanguis cells were attached to a Falcon 3001 tissue culture plates or bovine enamel chips, coated with a biological adhesive. Scanning electron microscopy of the chips showed the streptococci as a contiguous surface. Radiolabeled bacteria were used to measure a second-species interbacterial adherence to the streptococcal-coated culture plates. Strains of H. parainfluenzae known to coaggregate (strain HP-28) and not to coaggregate (strains HP-42 and HP-80), in suspension with S. sanguis strain SA-1, were studied for adherence. Ten-fold-higher numbers of coaggregating strain HP-28 adhered in vitro to the streptococcal layer than did the non-coaggregating strains. S. sobrinus strain 6715 did not show appreciable adherence to the S. sanguis surface. Saliva did not affect the adherence of coaggregating or non-coaggregating H. parainfluenzae strains to S. sanguis strain SA-1. Bovine enamel chips, coated with streptococci, mounted on modified orthodontic appliances and placed in the mouths of three volunteers, facilitated the measurement of interbacterial adherence in vivo of streptomycin-resistant strains of H. parainfluenzae (HP-28R or HP-42R). Suspensions of bacteria were placed into the mouth, distributed throughout, and expectorated. After 15 or 120 minutes, the appliance with the chips was removed, the chips sonified, and colony-forming units (CFU) of streptomycin-resistant haemophili determined per chip.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1988        PMID: 3198842     DOI: 10.1177/00220345880670120301

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  7 in total

1.  Insertional inactivation of an intrageneric coaggregation-relevant adhesin locus from Streptococcus gordonii DL1 (Challis).

Authors:  C J Whittaker; D L Clemans; P E Kolenbrander
Journal:  Infect Immun       Date:  1996-10       Impact factor: 3.441

2.  Purification and characterization of an outer membrane protein adhesin from Haemophilus parainfluenzae HP-28.

Authors:  C H Lai; C Bloomquist; W F Liljemark
Journal:  Infect Immun       Date:  1990-12       Impact factor: 3.441

3.  Adherence of mutans streptococci to other oral bacteria.

Authors:  R J Lamont; B Rosan
Journal:  Infect Immun       Date:  1990-06       Impact factor: 3.441

4.  Adhesion of Actinomyces viscosus to Porphyromonas (Bacteroides) gingivalis-coated hexadecane droplets.

Authors:  M Rosenberg; I A Buivids; R P Ellen
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

5.  Microbial Diversity in the Early In Vivo-Formed Dental Biofilm.

Authors:  D Heller; E J Helmerhorst; A C Gower; W L Siqueira; B J Paster; F G Oppenheim
Journal:  Appl Environ Microbiol       Date:  2016-01-08       Impact factor: 4.792

6.  Adherence, accumulation, and cell division of a natural adherent bacterial population.

Authors:  C G Bloomquist; B E Reilly; W F Liljemark
Journal:  J Bacteriol       Date:  1996-02       Impact factor: 3.490

7.  Coaggregation of Fusobacterium nucleatum, Selenomonas flueggei, Selenomonas infelix, Selenomonas noxia, and Selenomonas sputigena with strains from 11 genera of oral bacteria.

Authors:  P E Kolenbrander; R N Andersen; L V Moore
Journal:  Infect Immun       Date:  1989-10       Impact factor: 3.441

  7 in total

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