Our goal is to determine whether it is possible to tip the ecological balance in dental plaque in favor of oral microorganisms associated with health, rather than with disease. In pursuit of this goal, we will establish a functional genomics map of the genes and proteins involved in the oxidative stress response mechanisms of Streptococcus mutans, a causative agent of dental caries in humans. S. mutans relies on its stress-response systems to out-compete organisms such as Streptococcus sanguinis or S. gordonii, bacteria that are associated with oral health. The map of S. mutans oxidative stress responses will provide novel, and organism-specific, targets for the development of therapeutic agents to reduce or prevent dental caries. In the proposed project, we will use high-throughput proteomic and transcriptomic approaches to identify genes associated with the S. mutans oxidative stress response.
In Aim 1 of the project, we will use proteomics to identify proteins associated with the S. mutans oxidative stress response.
In Aim 2, we will use a complementary transcriptomic approach to establish the number of S. mutans genomic transcripts associated with the oxidative stress response.
In Aim 3, we will use an established collection of genetically barcoded deletion mutant strains of S. mutans, created by our laboratory, to assign mutant strains to the proteins and transcripts identified in Aims 1 and 2. This sub-library of mutant strains will be co-cultured with S. gordonii to determine the contribution of each gene in the sub-library to the ability of S. mutans to compete with S. gordonii.
In Aim 4, we will use the sub-library of mutant strains, identified in Aim 3, in the rat model of oral microbial infection, to determine the contribution of each oxidative stress gene to the ability of S. mutans to infect rats We will also use the deletion mutant sub-library to test sensitivity to compounds known to affect the ability of S. mutans to grow. In this way, we will identify metabolic pathways responsive to oxidative stress. Our long-term goal is to identify new, and possibly probiotic, mechanisms for reducing dental disease in humans.

Public Health Relevance

The proposed research project is designed to find new ways to prevent dental cavities in people. Dental cavities are caused by bacteria growing on teeth, most commonly by an organism called Streptococcus mutans. The goal of this research is to identify the S. mutans genes that are the most important for causing cavities and to use this information to develop new compounds that will prevent the disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE013683-13
Application #
9271956
Study Section
Special Emphasis Panel (ZRG1-MOSS-V (03)M)
Program Officer
Lunsford, Dwayne
Project Start
2000-09-15
Project End
2020-05-31
Budget Start
2017-06-01
Budget End
2018-05-31
Support Year
13
Fiscal Year
2017
Total Cost
$559,802
Indirect Cost
$156,109
Name
University of Rochester
Department
Microbiology/Immun/Virology
Type
Schools of Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Saputo, S; Faustoferri, R C; Quivey Jr, R G (2018) A Drug Repositioning Approach Reveals that Streptococcus mutans Is Susceptible to a Diverse Range of Established Antimicrobials and Nonantibiotics. Antimicrob Agents Chemother 62:
Baker, J L; Lindsay, E L; Faustoferri, R C et al. (2018) Characterization of the Trehalose Utilization Operon in Streptococcus mutans Reveals that the TreR Transcriptional Regulator Is Involved in Stress Response Pathways and Toxin Production. J Bacteriol 200:
Saputo, S; Faustoferri, R C; Quivey Jr, R G (2018) Vitamin D Compounds Are Bactericidal against Streptococcus mutans and Target the Bacitracin-Associated Efflux System. Antimicrob Agents Chemother 62:
Kovacs, C J; Faustoferri, R C; Quivey Jr, R G (2017) RgpF Is Required for Maintenance of Stress Tolerance and Virulence in Streptococcus mutans. J Bacteriol 199:
Baker, J L; Faustoferri, R C; Quivey Jr, R G (2017) Acid-adaptive mechanisms of Streptococcus mutans-the more we know, the more we don't. Mol Oral Microbiol 32:107-117
Solinski, Amy E; Koval, Alexander B; Brzozowski, Richard S et al. (2017) Diverted Total Synthesis of Carolacton-Inspired Analogs Yields Three Distinct Phenotypes in Streptococcus mutans Biofilms. J Am Chem Soc 139:7188-7191
Castillo Pedraza, Midian C; Novais, Tatiana F; Faustoferri, Roberta C et al. (2017) Extracellular DNA and lipoteichoic acids interact with exopolysaccharides in the extracellular matrix of Streptococcus mutans biofilms. Biofouling 33:722-740
Baker, Jonathon L; Faustoferri, Roberta C; Quivey Jr, Robert G (2016) A Modified Chromogenic Assay for Determination of the Ratio of Free Intracellular NAD+/NADH in Streptococcus mutans. Bio Protoc 6:
Cross, Benjamin; Faustoferri, Roberta C; Quivey Jr, Robert G (2016) What are We Learning and What Can We Learn from the Human Oral Microbiome Project? Curr Oral Health Rep 3:56-63
Cross, Benjamin; Garcia, Ariana; Faustoferri, Roberta et al. (2016) PlsX deletion impacts fatty acid synthesis and acid adaptation in Streptococcus mutans. Microbiology 162:662-71

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