Periodontitis affects about a third of the adult population, and it occurs in an aggressive form in approximately 1% of children. Its polymicrobial etiology is still incompletely understood. The oral microbiome consists of at least 600 species, and many of these have not yet been cultured in the laboratory. Recent, open-ended studies utilizing DNA-based methods have revealed a complex bacterial community structure, and new candidate species, many of them uncultivated, appear to be important in disease. Even for species with cultured representatives, the clonal laboratory isolates represent only a snapshot of the genomic diversity and physiological potential of the large number of lineages that represent that species in the heterogeneous human population. Our plan is to use large-scale small subunit ribosomal RNA (16S rRNA) analysis to determine the distribution and association of bacterial species in periodontitis as compared to periodontal health. We will conduct these studies in adults with recently active recurrent chronic periodontitis and children with newly diagnosed localized aggressive periodontitis, both as compared to matched, healthy individuals. We will then use this information to target uncultivated species and populations of bacteria specific to disease for metagenomic characterization, and to identify optimal human sources of samples for these studies. Since comprehensive genomic characterization of the oral microbiome by direct sequencing ('shotgun' metagenomics) is limited by the enormous microbial diversity and the uneven frequencies of the different organisms, we will use a novel approach, targeted metagenomics, to specifically separate and sequence the metagenomes of selected populations of uncultured bacteria from the oral microbiome. The proposed studies will provide a model approach to study uncultured subcomponents of the complex microbial communities that constitute the human microbiome by bridging the genomics of cultured, single lineage microbes with community shotgun metagenomics, This analysis will be integrated within a clinical and statistical framework, and will allow us to begin to elucidate the role of uncultivated members of the oral microbiome in human health and disease.

Public Health Relevance

Periodontitis is a disease that affects the bone and tissues that support the teeth, leading to tooth loss and systemic diseases. It is caused by bacteria, but there are so many species in the mouth that it has been difficult to figure out which ones cause disease. The proposed studies will use the latest next generation DNA sequencing approaches to learn which bacteria are important so that ways to prevent and treat disease may be developed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56DE021567-01
Application #
8121157
Study Section
Special Emphasis Panel (ZDE1-RW (22))
Program Officer
Lunsford, Dwayne
Project Start
2010-09-27
Project End
2013-08-31
Budget Start
2010-09-27
Budget End
2013-08-31
Support Year
1
Fiscal Year
2010
Total Cost
$522,134
Indirect Cost
Name
Ohio State University
Department
Dentistry
Type
Schools of Dentistry
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Campbell, Alisha G; Schwientek, Patrick; Vishnivetskaya, Tatiana et al. (2014) Diversity and genomic insights into the uncultured Chloroflexi from the human microbiota. Environ Microbiol 16:2635-43
Beall, Clifford J; Campbell, Alisha G; Dayeh, Daniel M et al. (2014) Single cell genomics of uncultured, health-associated Tannerella BU063 (Oral Taxon 286) and comparison to the closely related pathogen Tannerella forsythia. PLoS One 9:e89398
Campbell, Alisha G; Campbell, James H; Schwientek, Patrick et al. (2013) Multiple single-cell genomes provide insight into functions of uncultured Deltaproteobacteria in the human oral cavity. PLoS One 8:e59361