|
|
||||||||
The FASEB Journal, Vol 7, 406-413, Copyright © 1993 by The Federation of American Societies for Experimental Biology
REVIEWS |
PE Kolenbrander, N Ganeshkumar, FJ Cassels and CV Hughes
Laboratory of Microbial Ecology, National Institute of Dental Research, Bethesda, Maryland 20892.
Nearly all human oral bacteria exhibit coaggregation, cell-to-cell recognition of genetically distinct cell types. Clumps or coaggregates composed of the two kinds of cells are formed immediately upon mixing two partner cell types. Members of all 18 genera tested exhibit lactose- reversible coaggregation. Many of these interactions appear to be mediated by a lectin on one cell type that interacts with a complementary carbohydrate receptor on the other cell type. A lactose- sensitive adhesin has been isolated from Prevotella loescheii PK1295, and it exhibits the adherence properties observed with whole cells. Other adhesins have been identified and the genes for some of them have been cloned and sequenced. One Streptococcus sanguis adhesin is a lipoprotein that appears to have a dual function of recognizing both a bacterial carbohydrate receptor and a receptor in human saliva. Carbohydrate receptors for some adhesins have been purified from five oral streptococci, and they specifically block the coaggregations with the streptococcal partners that express the complementary adhesins. Coaggregation offers an explanation for the temporally related accretion of dental plaque and bacterial recognition of mucosal surfaces. Early colonizers of the tooth surface coaggregate with each other and late colonizers of the tooth surface coaggregate with each other, but with few exceptions, early colonizers do not recognize late colonizers. Furthermore, bacteria that colonize mucosal surfaces coaggregate with each other, indicating the high degree of specificity of coaggregation in the oral bacterial population.
This article has been cited by other articles:
![]() |
L. C. N. Brito, F. R. Teles, R. P. Teles, E. C. Franca, A. P. Ribeiro-Sobrinho, A. D. Haffajee, and S. S. Socransky Use of Multiple-Displacement Amplification and Checkerboard DNA-DNA Hybridization To Examine the Microbiota of Endodontic Infections J. Clin. Microbiol., September 1, 2007; 45(9): 3039 - 3049. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Li, Y. Ge, D. Saxena, and P. W. Caufield Genetic Profiling of the Oral Microbiota Associated with Severe Early-Childhood Caries J. Clin. Microbiol., January 1, 2007; 45(1): 81 - 87. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Yoshida, T. Ansai, T. Takehara, and H. K. Kuramitsu LuxS-Based Signaling Affects Streptococcus mutans Biofilm Formation Appl. Envir. Microbiol., May 1, 2005; 71(5): 2372 - 2380. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. P. Concannon, T. D. Crowe, J. J. Abercrombie, C. M. Molina, P. Hou, D. K. Sukumaran, P. A. Raj, and K. -P. Leung Susceptibility of oral bacteria to an antimicrobial decapeptide J. Med. Microbiol., December 1, 2003; 52(12): 1083 - 1093. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Davey and G. A. O'toole Microbial Biofilms: from Ecology to Molecular Genetics Microbiol. Mol. Biol. Rev., December 1, 2000; 64(4): 847 - 867. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Kataoka, A. Amano, S. Kawabata, H. Nagata, S. Hamada, and S. Shizukuishi Secretion of Functional Salivary Peptide by Streptococcus gordonii Which Inhibits Fimbria-Mediated Adhesion of Porphyromonas gingivalis Infect. Immun., August 1, 1999; 67(8): 3780 - 3785. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Marcotte and M. C. Lavoie Oral Microbial Ecology and the Role of Salivary Immunoglobulin A Microbiol. Mol. Biol. Rev., March 1, 1998; 62(1): 71 - 109. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |