Dental caries remains among the most prevalent infectious diseases worldwide. Over 84 percent of U.S. children, 96 percent of U.S. adults, and 99.5 percent of Americans 65 years of age and older have experienced tooth decay. Overall, caries appears not to be under control, even in industrialized countries. The best control strategies for caries involve reducing the virulence of the pathogens. Streptococcus mutans is recognized as the principal etiological agent of dental caries. The ability to metabolize carbohydrates and to adhere to and form tenacious biofilms on the tooth surfaces are believed to be critically associated with the cariogenicity of this human pathogen. Although numerous studies have elucidated the mechanisms of initial attachment, not all the factors that are involved in biofilm formation have been identified. Moreover, very little is known about the regulation of expression of these factors on the S. mutans cell-surfaces. Therefore, we have chosen to identify and study the expression of these cell surface proteins. We found that a functional HtrA (a serine protease needed for processing and maturation of proteins) is required for biofilm formation in S. mutans. Since we also found that HtrA modulates expression of various cell-surface proteins, we hypothesize that some of those HtrA regulated cell-surface proteins are required for biofilms. In this proposal, in Specific Aim 1, we will identify those cell-surface proteins that need functional HtrA. HtrA acts as both protease and chaperone. Because chaperone activity is needed for proper protein folding, we propose that chaperone activity is also involved in cell-surface expression of proteins.
In specific Aim 2, we will test this hypothesis using two cell-surface proteins, enolase and glyceraldehydes-3-phosphate dehydrogenease, that were affected by an htrA null mutation: A clearer understanding of the regulation of extracellular/cell-surface protein expression in S. mutans will provide opportunities for the development of new approaches to the prevention and treatment of dental caries. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Exploratory/Developmental Grants (R21)
Project #
7R21DE016056-03
Application #
7536298
Study Section
Special Emphasis Panel (ZDE1-YL (39))
Program Officer
Lunsford, Dwayne
Project Start
2006-07-01
Project End
2009-06-30
Budget Start
2008-01-01
Budget End
2009-06-30
Support Year
3
Fiscal Year
2007
Total Cost
$38,377
Indirect Cost
Name
University of Kansas
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Zhang, Jiaqin; Biswas, Indranil (2009) A phenotypic microarray analysis of a Streptococcus mutans liaS mutant. Microbiology 155:61-8
Banerjee, Anirban; Biswas, Indranil (2008) Markerless multiple-gene-deletion system for Streptococcus mutans. Appl Environ Microbiol 74:2037-42
Biswas, Indranil; Drake, Laura; Erkina, Dasha et al. (2008) Involvement of sensor kinases in the stress tolerance response of Streptococcus mutans. J Bacteriol 190:68-77
Biswas, Indranil; Jha, Jyoti K; Fromm, Nicholas (2008) Shuttle expression plasmids for genetic studies in Streptococcus mutans. Microbiology 154:2275-82
Biswas, Indranil; Drake, Laura; Biswas, Saswati (2007) Regulation of gbpC expression in Streptococcus mutans. J Bacteriol 189:6521-31
Biswas, Indranil; Drake, Laura; Johnson, Sean et al. (2007) Unmarked gene modification in Streptococcus mutans by a cotransformation strategy with a thermosensitive plasmid. Biotechniques 42:487-90