There is a growing awareness that oral treponemes play a role in the progression from health to periodontitis. Despite the interest in the relationship of this genus to periodontitis, only a few Treponema spp. have been isolated and grown. Substantial literature has implicated Treponema denticola as an oral pathogen: however, few investigations have examined other species. These investigators have discovered that the predominant cultivable oral spirochete in subgingival These investigators propose to investigate T. pectinovorum virulence components and its potential contribution to the tissue and cellular destruction observed vitro and in vivo models which have been developed during the initial phases of the grant. The hypothesis to be tested is that T. pectinovorum is a major this organism presents unique outer membrane proteins and an LPS-like molecule distinctive from other oral treponemes, the hypothesis to be tested is that the 42 kDa major outer membrane protein (MompA) and the LPS like molecule (LPSL) have characteristics of virulence components in in vitro and in vivo models of disease. Successful testing of these hypotheses would imply that T. pectinovorum utilizes these components in subgingival plaque ecology to contribute to the soft tissue destructive and bone resorptive manifestations of functions of the 42 kDa major outer membrane protein (MompA) of T. pectinovorum including i) cloning and sequencing the MompA gene, ii) developing Abs to localize the molecule and determine its distribution among T. pectinovorum isolates, and iii) determining functional characteristics of MompA including its role as an adhesin for epithelial cells and fibroblasts, its activity as a ligand in eliciting host cell cytokine responses, and determination of its antigens capacity in a murine model. A highly innovative aspect of these studies will investigate variations in binding and effects on host cell functions following interaction of T. pectinovorum with fibroblasts derived from normal and HIV-infected individuals; 2) To isolate and characterize the LPSL molecule from T. pectinovorum including: i) biochemical characterization of the LPSL, ii) determining the endotoxic activity in vitro and in vivo, and iii) examining its biological functions in vitro and in vivo; and 3) To evaluate the presence and level of T. pectinovorum in human plaque samples using molecular and immunologic probes, including i) species-specific probes for T. pectinovorum and other oral treponemes, ii)MompA probes: iii) intragenic probes for T. pectinovorum; iv) Antibody to the MompA, and v) Ab to the LPSL.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
2R01DE011368-04A1
Application #
2697008
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Project Start
1994-09-30
Project End
2003-04-30
Budget Start
1999-06-15
Budget End
2000-04-30
Support Year
4
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Dentistry
Type
Schools of Dentistry
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Holt, Stanley C; Ebersole, Jeffrey L (2005) Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia: the ""red complex"", a prototype polybacterial pathogenic consortium in periodontitis. Periodontol 2000 38:72-122
Kesavalu, L; Holt, S C; Ebersole, J L (2003) In vitro environmental regulation of Porphyromonas gingivalis growth and virulence. Oral Microbiol Immunol 18:226-33
Kesavalu, L; Chandrasekar, B; Ebersole, J L (2002) In vivo induction of proinflammatory cytokines in mouse tissue by Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans. Oral Microbiol Immunol 17:177-80
Kesavalu, Lakshmyya; Falk, Clinton W; Davis, Kenneth J et al. (2002) Biological characterization of lipopolysaccharide from Treponema pectinovorum. Infect Immun 70:211-7
Xu, Xiaoping; Kolodrubetz, David (2002) Construction and analysis of hemin binding protein mutants in the oral pathogen Treponema denticola. Res Microbiol 153:569-77
Xu, X; Holt, S C; Kolodrubetz, D (2001) Cloning and expression of two novel hemin binding protein genes from Treponema denticola. Infect Immun 69:4465-72
Nixon, C S; Steffen, M J; Ebersole, J L (2000) Cytokine responses to treponema pectinovorum and treponema denticola in human gingival fibroblasts. Infect Immun 68:5284-92
Walker, S G; Ebersole, J L; Holt, S C (1999) Studies on the binding of Treponema pectinovorum to HEp-2 epithelial cells. Oral Microbiol Immunol 14:165-71
Chu, L; Ebersole, J L; Holt, S C (1999) Hemoxidation and binding of the 46-kDa cystalysin of Treponema denticola leads to a cysteine-dependent hemolysis of human erythrocytes. Oral Microbiol Immunol 14:293-303
Chu, L; Ebersole, J L; Kurzban, G P et al. (1999) Cystalysin, a 46-kDa L-cysteine desulfhydrase from Treponema denticola: biochemical and biophysical characterization. Clin Infect Dis 28:442-50

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