Development of a mature biofilm on the tooth surface is an important component of bacterial survival and pathogenesis in the oral cavity. Although over the past years, the complexity of the oral biofilm has been rapidly revealed, understanding how bacteria build up mature pathogenic biofilms in a well- defined way, is still lacking, leading to difficulty in identifying and designing new targets for anti-biofilm therapies. Toward this end, the study of the major Streptococcus mutans autolysin AtlA, shown to be required for biofilm maturation, is a new, but critical pathway for a more complete understanding for biofilm development of this organism. The demonstrated ability of the AtlA pathway to modulate cell surface remodeling is a major driving force for the studies outlined in this proposal, providing a new paradigm for the complex biofilm process particularly as related to the cell surface structure and remodeling process. Under this scope, we will focus our efforts in three interrelated areas.
In Specific Aim1, we will elucidate how AtlA is functionally and structurally associated with the cell surface through analysis of repeat domains in the AtlA protein. In the Specific Aim 2, we hypothesize that surface localization and activity of AtlA are modulated primarily by the gene products encoded within the atlA operon. In this Aim, we also attempt to identify additional AtlA-associated components, enhancing our understanding of the architecture and function of AtlA on the cell surface. And in the Specific Aim 3, we will perform a pilot experiment in a mouse caries model to begin to analyze the in vivo impact of AtlA in S. mutans caries development. Overall, this application manipulates an as yet uncharacterized role of AtlA in S. mutans biofilm formation, and data derived from these proposed studies have a high potential to facilitate the development of innovative therapeutic strategies to treat dental caries, e.g. by interfering with the autolytic pathways necessary for the proper development of cariogenic biofilms. This project is also part of our long-term objective elucidating the molecular basis for biofilm maturation and its underlying mechanisms.

Public Health Relevance

Streptococcus mutans has been considered the primary causative agent of dental caries, and can also cause infective endocarditis in at-risk patients. Development of a mature biofilm is a central event in the pathogenesis of dental caries. The S. mutans AtlA autolysin represents a new and unexplored target for discovery and development of anti-biofilm agents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Small Research Grants (R03)
Project #
1R03DE023604-01A1
Application #
8702318
Study Section
NIDCR Special Grants Review Committee (DSR)
Program Officer
Lunsford, Dwayne
Project Start
2014-04-09
Project End
2016-03-31
Budget Start
2014-04-09
Budget End
2015-03-31
Support Year
1
Fiscal Year
2014
Total Cost
$112,313
Indirect Cost
$37,313
Name
University of Florida
Department
Dentistry
Type
Schools of Dentistry
DUNS #
969663814
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Rice, Kelly C; Turner, Matthew E; Carney, O'neshia V et al. (2017) Modification of the Streptococcus mutans transcriptome by LrgAB and environmental stressors. Microb Genom 3:e000104
Ahn, Sang-Joon; Rice, Kelly C (2016) Understanding the Streptococcus mutans Cid/Lrg System through CidB Function. Appl Environ Microbiol 82:6189-6203