As additional information regarding cell-to-cell recognitions among oral bacteria is discovered, it is becoming increasingly clear that a dynamic but organized microbial community exists in the oral cavity. The part of this complex community studied in this laboratory pertains especially to microbial ecology. Both gram- positive an gram-negative bacteria are tested as coaggregation partners. The concept of highly specific partnerships advanced by this laboratory gained additional support with the evidence that strains of Bacteroides gingivalis, a presumed periodontal pathogen, coaggregates with Fusobacterium nucleatum and Eubacterium nodatum, strains, that are also associated with periodontal disease, but not with any other oral strains. Some coaggregations are inhibited by lactose, which adds to the growing number of sugar-inhibitable pairings among the oral bacteria. An intensive survey of strains of Veillonella from the tongue, buccal mucosa, and saliva revealed that veillonellae from the tongue coaggregate with Streptococcus salivarius, also a tongue inhabitant, but not with subgingival bacteria. Whereas, veillonellae from subgingival plaque coaggregate with other subgingival bacteria but not with S. salivarius. These results provide the first direct evidence that coaggregation is tightly coupled to the ability of a strain to colonize a specific econiche. The results of each of these investigative approaches are focused on understanding the relationship of cell surface recognitions among oral bacteria and their role in microbial ecology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Intramural Research (Z01)
Project #
1Z01DE000273-10
Application #
3917100
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Dental & Craniofacial Research
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Periasamy, Saravanan; Kolenbrander, Paul E (2009) Aggregatibacter actinomycetemcomitans builds mutualistic biofilm communities with Fusobacterium nucleatum and Veillonella species in saliva. Infect Immun 77:3542-51
Periasamy, Saravanan; Chalmers, Natalia I; Du-Thumm, Laurence et al. (2009) Fusobacterium nucleatum ATCC 10953 requires Actinomyces naeslundii ATCC 43146 for growth on saliva in a three-species community that includes Streptococcus oralis 34. Appl Environ Microbiol 75:3250-7
Jakubovics, Nicholas S; Gill, Steven R; Iobst, Stacey E et al. (2008) Regulation of gene expression in a mixed-genus community: stabilized arginine biosynthesis in Streptococcus gordonii by coaggregation with Actinomyces naeslundii. J Bacteriol 190:3646-57
Bachrach, Gilad; Altman, Hamutal; Kolenbrander, Paul E et al. (2008) Resistance of Porphyromonas gingivalis ATCC 33277 to direct killing by antimicrobial peptides is protease independent. Antimicrob Agents Chemother 52:638-42
Yoshida, Yasuo; Palmer, Robert J; Yang, Jinghua et al. (2006) Streptococcal receptor polysaccharides: recognition molecules for oral biofilm formation. BMC Oral Health 6 Suppl 1:S12
Palmer Jr, Robert J; Diaz, Patricia I; Kolenbrander, Paul E (2006) Rapid succession within the Veillonella population of a developing human oral biofilm in situ. J Bacteriol 188:4117-24
Diaz, Patricia I; Chalmers, Natalia I; Rickard, Alexander H et al. (2006) Molecular characterization of subject-specific oral microflora during initial colonization of enamel. Appl Environ Microbiol 72:2837-48
Kolenbrander, Paul E; Palmer Jr, Robert J; Rickard, Alexander H et al. (2006) Bacterial interactions and successions during plaque development. Periodontol 2000 42:47-79
Rickard, Alexander H; Palmer Jr, Robert J; Blehert, David S et al. (2006) Autoinducer 2: a concentration-dependent signal for mutualistic bacterial biofilm growth. Mol Microbiol 60:1446-56
Diaz, Patricia I; Slakeski, Nada; Reynolds, Eric C et al. (2006) Role of oxyR in the oral anaerobe Porphyromonas gingivalis. J Bacteriol 188:2454-62

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