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Periodontal
(gum) disease affects a large percentage of the US
population. Work in our laboratory focuses on pathogenic
properties of microorganisms associated with periodontal
disease. Specific projects are outlined below:
1) Characterization of the mechanisms by which
Actinobacillus actinomycetemcomitans (a pathogen
associated with certain forms of periodontal disease)
transports potential virulence factors from the
intracellular to the extracellular environment.
2) Evaluation of bacterial typing systems in the genetic
characterization of oral pathogens. Bacterial typing
systems are fundamental for epidemiologic study of
colonizing clones or for tracing the transmission of
microorganisms from one individual to another. There is
evidence that using multiple typing systems is more
reliable and provides a higher discriminatory power than
any one typing system alone in genetic analysis of
bacteria. We hypothesized that a select panel of typing
systems previously not used with oral pathogens would
allow discrimination of different bacterial species as
well as different strains within a given species. We have
been investigating four polymerase chain reaction (PCR)-based
methods in examining genetic variability of eight
pathogens associated with periodontitis (Porphyromonas
gingivalis; Prevotella intermedia; Actinobacillus
actinomycetemcomitans; Tannerella forsynthesis; Treponema
denticola; Peptostreptococcus micros; Fusobacterium
nucleatum; Selenomonas noxia). The methods were: 1)
arbitrarily-primed (AP)-PCR; 2) repetitive extragenic
palindromic (REP)-PCR; 3) enterobacterial repetitive
intergenic consensus (ERIC)-PCR; and 4) BOX-PCR.
3) Evaluation of the efficacy of antimicrobial peptides
against oral biofilms. With the increasing development of
antimicrobial resistance to traditional antibiotics, new
technologies are needed to combat infections that cause
human disease. Oral infections are rarely life threatening
but have a significant impact on quality of life,
economics, and oral and systemic health. The use of
systemic antibiotics for the management of oral
infections, especially in cases of the biofilm-associated
diseases dental caries and periodontal disease, has not
received considerable support because of the implications
for the emergence of antibiotic resistance in medically
important pathogens. However, the use of topical
chemotherapeutic agents is gaining considerable support
but the development of such agents is lagging behind the
potential applications. We are evaluating the efficacy of
natural and synthetic antimicrobial peptides against oral
pathogens, grown both planktonically and in biofilms, in
an attempt to develop new agents to fight oral infections.
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Novak, KF, and DJ LeBlanc. Characterization of Plasmid pVT745 Isolated
from Actinobacillus actinomycetemcomitans. Plasmid 31: 31-39, 1994.
Novak, KF, LN Lee and DJ LeBlanc: Functional Analysis of pVT745, a
Plasmid from Actinobacillus actinomycetemcomitans. Oral Microbiology and
Immunology 13: 124-128, 1998.
Novak, KF, Nonnemacher, MR and Pourhamidi, J. Molecular Characterization
and Functional Analysis of a secA Gene Homolog in Actinobacillus
actinomycetemcomitans. Microbiology and Immunology 44:143-148, 2000.
Galli, DM, Chen, J, Novak, KF and LeBlanc, DJ. Nucleotide Sequence and
Analysis of Conjugative Plasmid pVT745. J Bact 183: 1585-1594,
2001.
Novak, KF, Dougherty, BA Pelaez, M. Actinobacillus actinomycetemcomitans
Harbors Type IV Secretion System Genes on a Plasmid and in the Chromosome.
Microbiology. 147:3027-3035, 2001.
Whitehead, AW, Novak, KF and Close, JM. Identification of factors influencing
matriculation decisions by dental school applicants. J Dent Edu 66:62-67. 2002
Whitehead AW and Novak KF. A Model for Assessing the Ethical
Environment in
Academic Dentistry. J Dent Edu. 67:1113-1121. 2003 |
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Karen Novak, D.D.S., M.S., Ph.D.
Associate Professor
Center for Oral Health Research
University of Kentucky
College of Dentistry
D448 Dental Science Building
Lexington, KY 40536-0297
Tel: (859) 323-8705
Fax: (859) 257-6566
Email: knova2@uky.edu |
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