Journal
JOURNAL OF CLINICAL PERIODONTOLOGY
Volume 30, Issue 11, Pages 990-995Publisher
BLACKWELL MUNKSGAARD
DOI: 10.1034/j.1600-051X.2003.00419.x
Keywords
checkerboard DNA-DNA hybridization technique; microorganisms; plaque formation
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Objective: To determine microbial changes that occur during plaque formation in a dentition free of gingival inflammation. Material and Methods: Ten subjects were recruited. The study included one preparatory period (2 weeks) and a plaque accumulation period (4 days). The volunteers exercised proper tooth cleaning methods, were scaled and received repeated professional mechanical tooth cleaning during the preparatory period. During the plaque accumulation period, the participants abstained from plaque control measures. Plaque was scored on the approximal surfaces of maxillary and mandibular premolars on Days 0, 1, 2 and 4 using a scale from 0 to 5 and according to the criteria of the Quigley and Hein Plaque Index (QHI). Supragingival plaque samples were obtained from the same intervals and surfaces and evaluated using a checkerboard DNA-DNA hybridization technique. Results: The mean QHI increased from 0 to 1.6 (Day 4). The total number of organisms on Day 0 averaged 140x10(5) and increased to about 210x10(5) after 4 days without oral hygiene. The most dominant species on Day 0 were members of the genus Actinomyces. These organisms comprised almost 50% of the microbiota evaluated. None of the Actinomyces species increased significantly during the 4 days. Some Streptococcus species increased significantly over time as well as species of the genera Capnocytophaga, Campylobacter, Fusobacteria and Actinomyces actinomycetemcomitans. Conclusion: In the present investigation, the preparatory phase established a situation with minimal gingival inflammation and close to zero amounts of dental plaque. The Day 0 plaque samples exhibited high proportions of Actinomyces species. During the 4 days of no oral hygiene, there was a small increase in total numbers of organisms as well as a modest increase in the proportion of disease-associated taxa such as species of the orange complex species.
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