Bacteria in the periodontal pocket can develop complex sessile communities that play a significant role in infection-induced periodontal disease. Data emerging from the oral microbiome project is facilitating a shift in the paradigm for infection-induced periodontal diseases. Bacteria like Porphyromonas gingivalis, Prevotella intermedia, Aggregatibacter (Actinobacillus) actinomycetemcomitans, Tannerella forsythia and Treponema denticola have previously been demonstrated to be major pathogens associated with periodontal diseases. However, recent developments including novel, culture-independent techniques have allowed the identification of as-yet-culturable and fastidious organisms in patients suffering from periodontitis. Collectively, these studies have demonstrated that changes in periodontal status are associated with shifts in the composition of the bacterial community in the periodontal pocket. Filifactor alocis, a Gram-positive, asaccharolytic, obligate anaerobic rod, is one of the marker organisms that is now identified to be significant to the pathogenetic structure of biofilms associated with periodontal inflammation and should be considered an important organism for periodontal disease. Further, in comparison to the other traditional periodontal pathogens, F. alocis is present in the periodontal pocket in higher numbers and is least detected in healthy or periodontitis resistant patients. Currently, there is little or no information on the pathogenesis of F. alocis. In our laboratory, preliminary studies of F. alocis showed non-gingipain protease and sialidase activities. In silico analysis revealed molecular relatedness of several virulence factors from F. alocis and P. gingivalis. F. alocis was more resistant to oxidative stress and its growth stimulated under those condition in contrast to P. gingivalis. Biofilm formation was significantly increased in co-culture. There was an increase in adherence and invasion of epithelial cells in co-culture compared with P. gingivalis or F. alocis mono-cultures. In those epithelial cells, endocytic vesicle mediated internalization was only observed during co-culture. The F. alocis clinical isolate D-62D had an increased invasive capacity in co-culture with P. gingivalis compared to the F. alocis ATCC 35896 strain. In addition, there was variation in the proteome of the clinical isolates compared to the ATCC 35896 strain. Hypothetical proteins and those known to be important virulence factors in other bacteria were indentified. Our observations, taken together, may suggest that F. alocis has virulence properties that may enhance its ability to survive/persist in the periodontal pocket and may play an important role in infection-induced periodontal disease. It is our hypothesis that in F. alocis, similar to other periodontal pathogens, multiple coordinately regulated mechanisms are significant in the pathogenicity of the organism. We wish to gain an understanding of F. alocis potential virulence factors and evaluate whether they contribute to its pathogenicity. The primary goal of this R21 application is to develop a genetic system and an animal model to evaluate the host response to and virulence potential of F. alocis.
The specific aims are: (1) To evaluate the specific role(s) of protease activity in the survival/pathogenicity of F. alocis. (2) o develop an animal model for testing the virulence potential of F. alocis. Collectively, the results from this study will establish basic information on the pathogenesis of F. alocis. It will generatea model system(s) that will yield important clues that will facilitate the development of novel therapeutic interventions to aid in the control and prevention of periodontal disease
The goal of this research is to establish basic information on the ability of Filifactor alocis to cause gum disease. This bacterium which was previously unrecognized is now proposed to be a diagnostic indicator of gum disease. Because of the success of this bacterium in the periodontal pocket, an understanding of components that may lead to its survival and persistence is vital. This information will lead to the identification of rime targets for the development of novel therapeutics that will have a positive impact on human health.
|Dou, Y; Aruni, W; Muthiah, A et al. (2016) Studies of the extracytoplasmic function sigma factor PG0162 in Porphyromonas gingivalis. Mol Oral Microbiol 31:270-83|
|Boutrin, M-C; Yu, Y; Wang, C et al. (2016) A putative TetR regulator is involved in nitric oxide stress resistance in Porphyromonas gingivalis. Mol Oral Microbiol 31:340-53|
|McKenzie, Rachelle M E; Henry, Leroy G; Boutrin, Marie-Claire et al. (2016) Role of the Porphyromonas gingivalis iron-binding protein PG1777 in oxidative stress resistance. Microbiology 162:256-67|
|Chioma, O; Aruni, A W; Milford, T-A et al. (2016) Filifactor alocis collagenase can modulate apoptosis of normal oral keratinocytes. Mol Oral Microbiol :|
|Aruni, A Wilson; Dou, Yuetan; Mishra, Arunima et al. (2015) The Biofilm Community-Rebels with a Cause. Curr Oral Health Rep 2:48-56|
|Aruni, A Wilson; Mishra, Arunima; Dou, Yuetan et al. (2015) Filifactor alocis--a new emerging periodontal pathogen. Microbes Infect 17:517-30|
|Dou, Y; Robles, A; Roy, F et al. (2015) The roles of RgpB and Kgp in late onset gingipain activity in the vimA-defective mutant of Porphyromonas gingivalis W83. Mol Oral Microbiol 30:347-60|
|McKenzie, R M E; Aruni, W; Johnson, N A et al. (2015) Metabolome variations in the Porphyromonas gingivalis vimA mutant during hydrogen peroxide-induced oxidative stress. Mol Oral Microbiol 30:111-27|
|Henry, Leroy G; Boutrin, Marie-Claire; Aruni, Wilson et al. (2014) Life in a Diverse Oral Community - Strategies for Oxidative Stress Survival. J Oral Biosci 56:63-71|
|Aruni, W; Chioma, O; Fletcher, H M (2014) Filifactor alocis: The Newly Discovered Kid on the Block with Special Talents. J Dent Res 93:725-32|
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