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Infection and Immunity, February 2000, p. 732-739, Vol. 68, No. 2
Department of Oral Biology and the
Periodontal Disease Research Center, University of Florida,
Gainesville, Florida 32610,1 and
Research Center for Advanced Science and Technology,
University of Tokyo, Komaba 4-6-1, Meguroku, Tokyo,
Japan2
Received 23 July 1999/Returned for modification 2 September
1999/Accepted 2 November 1999
Porphyromonas gingivalis is a major etiologic agent of
periodontitis, a chronic inflammatory disease that ultimately results in the loss of the supporting tissues of the teeth. Previous work has
demonstrated the usefulness of avirulent Salmonella
enterica serovar Typhimurium strains as antigen delivery systems
for protective antigens of pathogens that colonize or cross mucosal
surfaces. In this study, we constructed and characterized a recombinant S. enterica serovar Typhimurium avirulent vaccine strain
which expresses hemagglutinin A and carries no antibiotic resistance markers. HagA, a major virulence-associated surface protein, is a
potentially useful immunogen that contains an antigenic epitope which,
in humans, elicits an immune response that is protective against
subsequent colonization by P. gingivalis. The
hagA gene, including its promoter, was cloned into a
balanced-lethal Salmonella vector and transferred to the
vaccine strain. Heterologous expression of HagA was demonstrated in
both Escherichia coli JM109 and S. enterica
serovar Typhimurium vaccine strain
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Expression and Immunogenicity of Hemagglutinin A
from Porphyromonas gingivalis in an Avirulent
Salmonella enterica Serovar Typhimurium Vaccine
Strain

4072. The HagA epitope was
present in its native configuration as determined by immunochemistry and immunoelectron microscopy. Purified recombinant HagA was recognized by sera from mice immunized with the S. enterica serovar
Typhimurium vaccine strain. The HagA-specific antigen of the vaccine
was also found to be recognized by serum from a periodontal patient.
This vaccine strain, which expresses the functional hemagglutinin
protein, induces a humoral immune response against HagA and may be
useful for developing a protective vaccine against periodontal diseases associated with P. gingivalis.
*
Corresponding author. Mailing address: Department of
Oral Biology, University of Florida, Box 100424 JHMHSC, Gainesville, FL
32610-0424. Phone: (352) 392-5937. Fax: (352) 392-2361. E-mail: kozarov{at}dental.ufl.edu.
Present address: Hoechst Marion Roussel Ltd., Minato Ward,
Tokyo, Japan 107-8465.
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