Periodontal diseases are biofilm-induced pathologies mediated by out-growth of commensal pathogens that live within a complex microbial community in the oral cavity. The development and function of this community depends on an array of cell-to-cell interactions and communication networks that rely on small molecules. There is little known regarding the nature of the signals, and the mechanisms as to how they are sensed and transmitted. This represents a major gap in knowledge. Determining the signals that promote colonization and growth (biofilm formation) of oral pathogens is fundamental to the development of therapeutic strategies. We have identified an extracellular arginine deiminase (ADI) produced by oral streptococci that acts on the oral pathogen Porphyromonas gingivalis, inhibiting its biofilm formation and expression of virulence determinants. The goal of this application is to determine the mechanism through which ADI signals P. gingivalis. A comprehensive set of experiments has been outline to test the central hypothesis that in addition to its key role in anaerobic growth and pH homeostasis of the oral biofilm, ADI acts as an effector protein.
The aims are to characterize the action of ADI on P. gingivalis biofilm development and to determine if ADI interacts directly with the surface of P. gingivalis cells. In addition, the molecular mechanism by which P. gingivalis senses ADI will be explored. Specifically, the studies will determine the transcriptional and physiological affect of ADI signaling on P. gingivalis through whole genome transcriptional studies, genetic screening, and direct visualization of biofilms using confocal microscopy. The overall goal of the proposal is to synthesize the data and develop a model as to how ADI signaling plays a role in vivo. This will advance the long-term goal to provide a basic understanding of the communication mechanisms that control colonization and out-growth of P. gingivalis, with the ultimate goal being to develop therapeutic strategies to prevent or treat periodontal disease.

Public Health Relevance

Periodontal disease is a chronic inflammatory disease, afflicting up to 50% of the adult population in the United States and persistent infections are associated with systemic diseases, such as diabetes, cardiovascular disease, and stroke. Annual costs for the prevention and treatment of periodontal diseases are over $14 billion. The proliferation of anaerobic bacteria in the subgingival biofilm community is central to progression of this chronic disease, with Porphyromonas gingivalis being implicated as one of the primary pathogens. The goal of this fellowship is to increase our understanding of a novel interspecies signaling system that modulates biofilm growth and virulence of this oral pathogen.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32DE022484-01A1
Application #
8314447
Study Section
NIDCR Special Grants Review Committee (DSR)
Program Officer
Frieden, Leslie A
Project Start
2012-03-01
Project End
2015-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
1
Fiscal Year
2012
Total Cost
$51,742
Indirect Cost
Name
Forsyth Institute
Department
Type
DUNS #
062190616
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Cugini, Carla; Stephens, Danielle N; Nguyen, Daniel et al. (2013) Arginine deiminase inhibits Porphyromonas gingivalis surface attachment. Microbiology 159:275-85
Cugini, Carla; Klepac-Ceraj, Vanja; Rackaityte, Elze et al. (2013) Porphyromonas gingivalis: keeping the pathos out of the biont. J Oral Microbiol 5: