Todd O. Kitten, Ph.D.
- Associate Professor of Oral & Craniofacial Molecular Biology and Microbiology &
Immunology
- Member Scientist, VCU Philips Institute
Office Location: Wood Building, Room 407
P.O. Box: 980566
Phone: (804) 628-7010
Fax: (804) 828-0150
E-mail: tkitten@vcu.edu
Lab Web Page:
http://www.people.vcu.edu/~tkitten
Research Interests
Research in our lab concerns bacteria that live in the mouth and their relationship to health and
disease. We are particularly interested in Streptococcus sanguinis, an important primary colonizer of
teeth and a frequent cause of a heart infection known as infective endocarditis. The picture at left shows
a transmission electron micrograph of S. sanguinis cells within an infected heart valve.
Along with other investigators at VCU, we recently determined
the DNA sequence of the S. sanguinis genome. We have used this information to identify potential
virulence factors for endocarditis, including 32 cell wall-anchored (also called "LPxTG") proteins and 52
lipoproteins. We have mutagenized the genes encoding each of these proteins and have tested the mutants for
endocarditis virulence. LPxTG proteins function principally as adhesins and exoenzymes whereas lipoproteins
function primarily in transport and post-translational modification. The figure below depicts these two
classes of proteins.
We have found that the SsaB transport lipoprotein is particularly important for endocarditis virulence.
Mutation of its gene results in a >1000-fold reduction in competitiveness in an endocarditis model. We
are currently working to determine the mechanism by which SsaB contributes to disease.
S. sanguinis cells possess the ability to incorporate foreign DNA from their environment into their
genomeāa property known as genetic competence. The figure below illustrates the major components of the
competence system in S. sanguinis.
We are interested in examining this system because (i) competence likely plays an important role in genome
evolution and adaptability (ii) the competence system likely possesses functions in addition to DNA uptake,
including contributing to biofilm formation in dental plaque, and (iii) the system in S. sanguinis appears to
possess important differences relative to characterized systems in other bacteria. We are currently examining
the genetic regulation of the competence system, and its possible contribution to endocarditis virulence and
biofilm formation.
Honors
- 2007, 2008: Special Reviewer, NIH ODCS Study Section
- 2007: Reviewer, NIDCR Special Emphasis Panel
- 2006: Reviewer, NIH-RAID proposal review meeting
- 2006: Special Reviewer, NIH ODCS member conflict panel, 2006
- 2003: Special Reviewer, NIH Oral, Dental and Craniofacial Sciences (ODCS) study section
Funded Research
- R01AI47841: Streptococcal virulence factors in extra-oral disease
- R01DE18138 (Xu, PI) : Regulation of fitness and virulence in oral streptococci
- C-VCU-07: Genetic competence in Streptococcus sanguinis.
Selected Publications
- Das S, Kanamoto T, Ge X, Xu P, Unoki T, Munro CL, Kitten T. (2009) Contribution
of lipoproteins and lipoprotein processing to endocarditis virulence in Streptococcus sanguinis.
J. Bacteriol.: in press.
- Ge X, Kitten T, Chen Z, Lee SP, Munro CL, Xu P. (2008) Identification of
Streptococcus sanguinis genes required for biofilm formation and examination of their role in endocarditis
virulence. Infect Immun 76:2551-2559.
- Tang G, Kitten T, Munro CL, Wellman GC, Mintz KP. (2008) EmaA, a potential virulence
determinant of Aggregatibacter (Actinobacillus) actinomycetemcomitans in infective endocarditis. Infect
Immun 76:2316-2324.
- Xu P, Alves JM, Kitten T, Power A, Chen Z, Manque P, Ge X, Serrano MG, Ozaki LS,
Akan D, Hendricks S, Wang Y, Puiu D, Chaplin M, Paik S, Peterson DL, Macrina FL, Buck GA. (2007) Genome
of the opportunistic pathogen Streptococcus sanguinis. J. Bacteriol. 189:3166-3175.
- Paik S, Senty L, Das S, Noe JC, Munro CL, Kitten T. (2005) Identification of virulence
determinants for endocarditis in Streptococcus sanguinis by signature-tagged mutagenesis. Infect Immun 73:6064-6074.
- Das S, Noe JC, Paik S, Kitten T. (2005) An improved arbitrary primed PCR method for rapid
characterization of transposon insertion sites. J Microbiol Methods 63: 89-94.