The rodent has been used for a number of years as a model system for the
production of human dental caries. (1) the rat has provided to be a
suitable model since caries can be readily induced, and the results are in
general reproducible (1,2,3). Valuable insights into the cariogenicity of
individual bacterial species has been obtained (4,5). More recently the
role of host immune factors in the modulation and control of dental caries
has been extensively studied in the rat and in the hamster (2,3) and have
revealed that either oral or submucosal immunization may protect against
caries (2,3,4). In spite of the wealth of data in this field, little is
known about the bacterial interrelationships in relation to bacterial
colonization and dental caries. In the in vitro model of caries important
differences in the production of caries have been found when more than one
species of bacteria is used in the model (Heilman and Clarkson). It has
been shown that when S. mutans and A. viscossus are fermented with sucrose
in the presence of teeth, subsurface lesions in enamel developed with S.
mutans and much smaller or no lesions developed with A. viscossus. As no
pH differences were detected (both were at pH 4.5) and the teeth were
suspended in the media for the same length of time, these results were
surprising. However, in the same system both bacteria produced comparable
lesions on the root surface. Further investigations are planned to: mix
the bacterial strains; to monoinnoculate with S. mutans and then innoculate
with the A. Viscossus (to reverse this); to vary the fermation conditions;
and to introduce immunological and nonimmunological factors into the
system. We wish to extend the in vitro work into a suitable model in vivo,
and to be able to study the effects of saliva and host immunological
factors on the colonization of bacteria, and on the subsequent development
of caries. The rat was selected since this is currently the most well
studied animal model and has been shown to be reproducible. For the study
of individual bacterial species it is necessary to use a gntobiotic unit.
National Institute of Dental and Craniofacial Research
CFDA Code
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062761671
UEI
Z1H9VJS8NG16
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