Periodontitis is a widespread and costly disease that is primarily manifest in the oral cavity but is also associated with systemic dieases such as atherosclerosis and rheumatoid arthritis. Although several organisms have been identified as periodontal pathogens, A. actinomycetemcomitans has been strongly associated with aggressive forms of periodontitis. Our prior work showed that quorum sensing is essential for A. actinomycetemcomitans virulence and we identified the QseBC two component system as a critical component of the quorum sensing pathway. Our new results suggest that QseBC may interact with catecholamine hormones produced by the host and thus, QseBC may mediate both cell density dependent signaling and inter-kingdom signaling. This application focuses on the mechanisms of interaction of the two component system with catecholamine hormones and is potential role in regulating iron uptake by A. actinomycetemcomitans.
Aim 1 will determine if catecholamine hormones and iron represent signals that activate QseBC and identify functional motifs of the QseC sensor that are required for binding. The genes that are regulated upon activation of QseBC will also be identifed using genomic microarrays.
Aim 2 will study an operon encoding a putative enterobactin receptor and transporter and determine if this receptor interacts with catecholamine-iron complexes. The contribution of the enterobactin receptor to virulence will also be examined using a mouse model of periodontitis. We have also shown that QseBC may be coupled to the cell stress response through the activity of two iron responsive toxin-antitoxin (TA) systems. This regulatory network will be studied in Aim 3 to determine if the expression of stress proteases is induced under iron limiting conditions and whether these proteases activate the TA toxins by degrading the labile antitoxin. The effect of TA toxin activation on the expression of QseBC and virulence of A. actinomycetemcomitans will also be determined. The overall goal of this study is to better understand the functional outcomes of activation of the essential QseBC two component system and how signaling through QseBC contributes to virulence.

Public Health Relevance

Periodontitis is a common oral disease that is present in up to 40% of the adult population in the United States. Annual expenditures for treatment and prevention of periodontitis exceed $15 billion. Although periodontitis is primarily manifest i the oral cavity, it is also associated with systemic illnesses such as heart disease and rheumatoid arthritis. Our recent studies suggest that the periodontal pathogen A. actinomycetemcomitans interacts with host hormones and iron and that this interaction contributes to its virulence. This study will characterize the bacterial proteins that are invoved in this interaction in order to understand their role in disease. These proteins represent new potential targets for therapies that may control or prevent periodontitis and the systemic illnesses associated with this disease.

National Institute of Health (NIH)
National Institute of Dental & Craniofacial Research (NIDCR)
Research Project (R01)
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Oral, Dental and Craniofacial Sciences Study Section (ODCS)
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Lunsford, Dwayne
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University of Louisville
Schools of Dentistry/Oral Hygn
United States
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Schneider, B; Weigel, W; Sztukowska, M et al. (2018) Identification and functional characterization of type II toxin/antitoxin systems in Aggregatibacter actinomycetemcomitans. Mol Oral Microbiol 33:224-233
Weigel, W A; Demuth, D R (2016) QseBC, a two-component bacterial adrenergic receptor and global regulator of virulence in Enterobacteriaceae and Pasteurellaceae. Mol Oral Microbiol 31:379-97
Weigel, W A; Demuth, D R; Torres-Escobar, A et al. (2015) Aggregatibacter actinomycetemcomitans QseBC is activated by catecholamines and iron and regulates genes encoding proteins associated with anaerobic respiration and metabolism. Mol Oral Microbiol 30:384-98
Torres-Escobar, Ascención; Juárez-Rodríguez, María D; Demuth, Donald R (2014) Integration host factor is required for replication of pYGK-derived plasmids in Aggregatibacter actinomycetemcomitans. FEMS Microbiol Lett 357:184-94
Juárez-Rodríguez, María Dolores; Torres-Escobar, Ascención; Demuth, Donald R (2014) Transcriptional regulation of the Aggregatibacter actinomycetemcomitans ygiW-qseBC operon by QseB and integration host factor proteins. Microbiology 160:2583-94
Torres-Escobar, Ascención; Juárez-Rodríguez, María Dolores; Demuth, Donald R (2014) Differential transcriptional regulation of Aggregatibacter actinomycetemcomitans lsrACDBFG and lsrRK operons by integration host factor protein. J Bacteriol 196:1597-607
Wright, C J; Burns, L H; Jack, A A et al. (2013) Microbial interactions in building of communities. Mol Oral Microbiol 28:83-101
Juárez-Rodríguez, María Dolores; Torres-Escobar, Ascención; Demuth, Donald R (2013) ygiW and qseBC are co-expressed in Aggregatibacter actinomycetemcomitans and regulate biofilm growth. Microbiology 159:989-1001
Torres-Escobar, Ascencion; Juarez-Rodriguez, Maria Dolores; Lamont, Richard J et al. (2013) Transcriptional regulation of Aggregatibacter actinomycetemcomitans lsrACDBFG and lsrRK operons and their role in biofilm formation. J Bacteriol 195:56-65
Juarez-Rodriguez, Maria Dolores; Torres-Escobar, Ascencion; Demuth, Donald R (2013) Construction of new cloning, lacZ reporter and scarless-markerless suicide vectors for genetic studies in Aggregatibacter actinomycetemcomitans. Plasmid 69:211-22

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