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Infection and Immunity, May 2001, p. 3048-3056, Vol. 69, No. 5
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.5.3048-3056.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Porphyromonas gingivalis Gingipains and Adhesion to
Epithelial Cells
Tsute
Chen,1
Koji
Nakayama,2
Lynn
Belliveau,1 and
Margaret J.
Duncan1,*
Department of Molecular Genetics, The Forsyth
Institute, Boston, Massachusetts 02115,1 and
Department of Microbiology, Faculty of Dentistry, Nagasaki
University, Nagasaki, Japan2
Received 16 November 2000/Returned for modification 4 January
2001/Accepted 8 February 2001
Porphyromonas gingivalis is one of the principal
organisms associated with adult periodontitis. Bacterial surface
proteins such as fimbriae and gingipain hemagglutinin domains have been implicated as adhesins that actuate colonization of epithelium lining
the gingival sulcus. We investigated the genetics of P. gingivalis adhesion to monolayers of epithelial cells using
wild-type and gingipain mutant strains. These experiments suggested
that arginine-specific gingipain (Rgp) catalytic activity modulated adhesion. From the data obtained with rgp mutants, we
constructed a working hypothesis predicting that attachment and
detachment of P. gingivalis to epithelial cells were
mediated by gingipain adhesin and Rgp catalytic domains, respectively.
A membrane-based epithelial cell binding assay, used to locate adhesins
in extracellular fractions of wild-type and mutant strains, recognized
gingipain peptides as adhesins rather than fimbriae. We developed a
capture assay that demonstrated the binding of gingipain adhesin
peptides to oral epithelial cells. The adherence of fimbrillin to
epithelial cells was detected after heat denaturation of cell
fractions. The prediction that Rgp catalytic activities mediated
detachment was substantiated when the high level of attachment of an
rgp mutant was reduced in the presence of wild-type cell
fractions that contained gingipain catalytic activities.
*
Corresponding author. Mailing address: Department of
Molecular Genetics, The Forsyth Institute, 140 Fenway, Boston, MA
02115. Phone: (617) 262-5200, ext. 344. Fax: (617) 262-4021. E-mail: mduncan{at}forsyth.org.
Infection and Immunity, May 2001, p. 3048-3056, Vol. 69, No. 5
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.5.3048-3056.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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