Microbiota of health, gingivitis, and initial periodontitis

. This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3‐month intervals...

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Vydáno v:	Journal of clinical periodontology Ročník 25; číslo 2; s. 85 - 98
Hlavní autoři:	Tanner, A., Maiden, M. F. J., Macuch, P. J., Murray, L. L., Kent Jr, R. L.
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Oxford, UK Blackwell Publishing Ltd 01.02.1998
Témata:	Adult Bacteroidaceae - isolation & purification Bacteroidaceae - pathogenicity Bacteroides - isolation & purification Bacteroides - pathogenicity Campylobacter - isolation & purification Campylobacter - pathogenicity Cluster Analysis Colony Count, Microbial Dental Plaque - metabolism Disease Progression DNA Probes DNA, Bacterial - analysis Female Gingiva - microbiology Gingival Recession - microbiology Gingivitis - microbiology Gram-Negative Bacteria - isolation & purification Gram-Positive Bacteria - isolation & purification Humans initial periodontitis Longitudinal Studies Male microbiology microbiota Middle Aged Periodontal Attachment Loss - microbiology periodontal disease Periodontitis - microbiology Statistics, Nonparametric
ISSN:	0303-6979, 1600-051X
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Abstract	. This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3‐month intervals for 12 months. More sites demonstrated small increments of attachment loss than attachment gain over the monitoring period. Sites, from 17 subjects, showing ≥1.5 mm periodontal attachment loss during monitoring were sampled as active lesions for microbial analysis. Twelve subjects demonstrated interproximal lesions, and 5 subjects had attachment loss at buccal sites (recession). Cultural studies identified Bacteroides forsythus, Campylobacter rectus, and Selenomonas noxia as the predominant species associated with active interproximal lesions (9 subjects), whereas Actinomyces naeslundii, and Streptococcus oralis, were the dominant species colonizing buccal active sites. A. naesludii, Campylobacter gracilis, and B. forsythus (at lower levels than active sites) were the dominant species cultured from gingivitis (10 subjects). Health‐associated species (10 subjects) included Streptococcus oralis, A. naeslundii, and Actinomyces gerencseriae. DNA probe data identified higher mean levels of B. forsythus and C. rectus with active (7 subjects) compared to inactive periodontitis sites. Porphyromonas gingivalls and Actinobacillus actinomycetemcomitans were detected infrequently. Cluster analysis of the cultural microbiota grouped 8/9 active interproximal lesions in one subcluster characterized by a mostly gram‐negative microbiota, including B. forsythus and C. rectus. The data suggest that B. forsythus C. rectus and S. noxia were major species characterizing sites converting from periodontal health to disease. The differences in location and microbiota of interproximal and buccal active sites suggested that different mechanisms may be involved in increased attachment loss.
AbstractList	This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3-month intervals for 12 months. More sites demonstrated small increments of attachment loss than attachment gain over the monitoring period. Sites, from 17 subjects, showing > or = 1.5 mm periodontal attachment loss during monitoring were sampled as active lesions for microbial analysis. Twelve subjects demonstrated interproximal lesions, and 5 subjects had attachment loss at buccal sites (recession). Cultural studies identified Bacteroides forsythus, Campylobacter rectus, and Selenomonas noxia as the predominant species associated with active interproximal lesions (9 subjects), whereas Actinomyces naeslundii, and Streptococcus oralis, were the dominant species colonizing buccal active sites. A. naeslundii, Campylobacter gracilis, and B. forsythus (at lower levels than active sites) were the dominant species cultured from gingivitis (10 subjects). Health-associated species (10 subjects) included Streptococcus oralis, A. naeslundii, and Actinomyces gerencseriae. DNA probe data identified higher mean levels of B. forsythus and C. rectus with active (7 subjects) compared to inactive periodontitis sites. Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans were detected infrequently. Cluster analysis of the cultural microbiota grouped 8/9 active interproximal lesions in one subcluster characterized by a mostly gram-negative microbiota, including B. forsythus and C. rectus. The data suggest that B. forsythus C. rectus and S. noxia were major species characterizing sites converting from periodontal health to disease. The differences in location and microbiota of interproximal and buccal active sites suggested that different mechanisms may be involved in increased attachment loss.This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3-month intervals for 12 months. More sites demonstrated small increments of attachment loss than attachment gain over the monitoring period. Sites, from 17 subjects, showing > or = 1.5 mm periodontal attachment loss during monitoring were sampled as active lesions for microbial analysis. Twelve subjects demonstrated interproximal lesions, and 5 subjects had attachment loss at buccal sites (recession). Cultural studies identified Bacteroides forsythus, Campylobacter rectus, and Selenomonas noxia as the predominant species associated with active interproximal lesions (9 subjects), whereas Actinomyces naeslundii, and Streptococcus oralis, were the dominant species colonizing buccal active sites. A. naeslundii, Campylobacter gracilis, and B. forsythus (at lower levels than active sites) were the dominant species cultured from gingivitis (10 subjects). Health-associated species (10 subjects) included Streptococcus oralis, A. naeslundii, and Actinomyces gerencseriae. DNA probe data identified higher mean levels of B. forsythus and C. rectus with active (7 subjects) compared to inactive periodontitis sites. Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans were detected infrequently. Cluster analysis of the cultural microbiota grouped 8/9 active interproximal lesions in one subcluster characterized by a mostly gram-negative microbiota, including B. forsythus and C. rectus. The data suggest that B. forsythus C. rectus and S. noxia were major species characterizing sites converting from periodontal health to disease. The differences in location and microbiota of interproximal and buccal active sites suggested that different mechanisms may be involved in increased attachment loss. . This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3‐month intervals for 12 months. More sites demonstrated small increments of attachment loss than attachment gain over the monitoring period. Sites, from 17 subjects, showing ≥1.5 mm periodontal attachment loss during monitoring were sampled as active lesions for microbial analysis. Twelve subjects demonstrated interproximal lesions, and 5 subjects had attachment loss at buccal sites (recession). Cultural studies identified Bacteroides forsythus, Campylobacter rectus, and Selenomonas noxia as the predominant species associated with active interproximal lesions (9 subjects), whereas Actinomyces naeslundii, and Streptococcus oralis, were the dominant species colonizing buccal active sites. A. naesludii, Campylobacter gracilis, and B. forsythus (at lower levels than active sites) were the dominant species cultured from gingivitis (10 subjects). Health‐associated species (10 subjects) included Streptococcus oralis, A. naeslundii, and Actinomyces gerencseriae. DNA probe data identified higher mean levels of B. forsythus and C. rectus with active (7 subjects) compared to inactive periodontitis sites. Porphyromonas gingivalls and Actinobacillus actinomycetemcomitans were detected infrequently. Cluster analysis of the cultural microbiota grouped 8/9 active interproximal lesions in one subcluster characterized by a mostly gram‐negative microbiota, including B. forsythus and C. rectus. The data suggest that B. forsythus C. rectus and S. noxia were major species characterizing sites converting from periodontal health to disease. The differences in location and microbiota of interproximal and buccal active sites suggested that different mechanisms may be involved in increased attachment loss. This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3-month intervals for 12 months. More sites demonstrated small increments of attachment loss than attachment gain over the monitoring period. Sites, from 17 subjects, showing > or = 1.5 mm periodontal attachment loss during monitoring were sampled as active lesions for microbial analysis. Twelve subjects demonstrated interproximal lesions, and 5 subjects had attachment loss at buccal sites (recession). Cultural studies identified Bacteroides forsythus, Campylobacter rectus, and Selenomonas noxia as the predominant species associated with active interproximal lesions (9 subjects), whereas Actinomyces naeslundii, and Streptococcus oralis, were the dominant species colonizing buccal active sites. A. naeslundii, Campylobacter gracilis, and B. forsythus (at lower levels than active sites) were the dominant species cultured from gingivitis (10 subjects). Health-associated species (10 subjects) included Streptococcus oralis, A. naeslundii, and Actinomyces gerencseriae. DNA probe data identified higher mean levels of B. forsythus and C. rectus with active (7 subjects) compared to inactive periodontitis sites. Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans were detected infrequently. Cluster analysis of the cultural microbiota grouped 8/9 active interproximal lesions in one subcluster characterized by a mostly gram-negative microbiota, including B. forsythus and C. rectus. The data suggest that B. forsythus C. rectus and S. noxia were major species characterizing sites converting from periodontal health to disease. The differences in location and microbiota of interproximal and buccal active sites suggested that different mechanisms may be involved in increased attachment loss. This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe, checkerboard hybridization method. 56 healthy adult subjects with minimal periodontal attachment loss were clinically monitored at 3‐month intervals for 12 months. More sites demonstrated small increments of attachment loss than attachment gain over the monitoring period. Sites, from 17 subjects, showing ≥1.5 mm periodontal attachment loss during monitoring were sampled as active lesions for microbial analysis. Twelve subjects demonstrated interproximal lesions, and 5 subjects had attachment loss at buccal sites (recession). Cultural studies identified Bacteroides forsythus, Campylobacter rectus , and Selenomonas noxia as the predominant species associated with active interproximal lesions (9 subjects), whereas Actinomyces naeslundii , and Streptococcus oralis , were the dominant species colonizing buccal active sites. A. naesludii, Campylobacter gracilis , and B. forsythus (at lower levels than active sites) were the dominant species cultured from gingivitis (10 subjects). Health‐associated species (10 subjects) included Streptococcus oralis, A. naeslundii , and Actinomyces gerencseriae. DNA probe data identified higher mean levels of B. forsythus and C. rectus with active (7 subjects) compared to inactive periodontitis sites. Porphyromonas gingivalls and Actinobacillus actinomycetemcomitans were detected infrequently. Cluster analysis of the cultural microbiota grouped 8/9 active interproximal lesions in one subcluster characterized by a mostly gram‐negative microbiota, including B. forsythus and C. rectus. The data suggest that B. forsythus C. rectus and S. noxia were major species characterizing sites converting from periodontal health to disease. The differences in location and microbiota of interproximal and buccal active sites suggested that different mechanisms may be involved in increased attachment loss.
Author	Tanner, A. Macuch, P. J. Maiden, M. F. J. Kent Jr, R. L. Murray, L. L.
Author_xml	– sequence: 1 givenname: A. surname: Tanner fullname: Tanner, A. email: atanner@forsyth.org organization: Forsyth Dental Center, Boston, Massachusetts 02115, USA – sequence: 2 givenname: M. F. J. surname: Maiden fullname: Maiden, M. F. J. organization: Forsyth Dental Center, Boston, Massachusetts 02115, USA – sequence: 3 givenname: P. J. surname: Macuch fullname: Macuch, P. J. organization: Forsyth Dental Center, Boston, Massachusetts 02115, USA – sequence: 4 givenname: L. L. surname: Murray fullname: Murray, L. L. organization: Forsyth Dental Center, Boston, Massachusetts 02115, USA – sequence: 5 givenname: R. L. surname: Kent Jr fullname: Kent Jr, R. L. organization: Forsyth Dental Center, Boston, Massachusetts 02115, USA
BackLink	https://www.ncbi.nlm.nih.gov/pubmed/9495607$$D View this record in MEDLINE/PubMed
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References	Moore, W. E., Moore, L. H., Ranney, R. R., Smibert, R. M., Burmeister, J. A, & Schenkein, H. A. (1991) The microflora of periodontal sites showing active destructive progression. Journal of Clinical Periodontology 18, 729-739. Tanner, A., Kent, R., Maiden, M. F. J. & Taubman, M. A. (1996) Clinical, microbiological and immunological profile of health, gingivitis and putative active periodontal subjects. Journal of Periodontal Research 31, 195-204. Gmur, R., Strub, J. R. & Guggenheim, B. (1989) Prevalence of Bacteroides forsythus and Bacteroides gingivalis in subgingival plaque of prosthodontically treated patients on short recall. Journal of Periodontal Research, 113-120. Moore, W. E., Holdeman, L. V. Smibert, R. M., Good, I. J., Burmeister, J. A., Palcanis, K. G. & Ranney, R. R. (1982) Bacteriology of experimental gingivitis in young adult humans. Infection & Immunity 38, 651-667. Haber, J. (1994) Smoking is a major risk factor for periodontitis. Current Opinion in Periodontology 00, 12-18. van Steenbergen, T. J., Petit, M. D., Scholte, L. H., Van der Velden, U. & de Graaff, J. (1993) Transmission of Porphyromonas gingivalis between spouses. Journal of Clinical Periodontology 20, 340-345. Loesche, W. J. & Syed, S. A. (1978) Bacteriology of human experimental gingivitis: effect of plaque and gingivitis score. Infection & Immunity 21, 830-839. Listgarten, M. A., Schifter, C. C. & Laster, L. (1985) 3-year longitudinal study of the periodontal status of an adult population with gingivitis. Journal of Clinical Periodontology 12, 225-238. McNabb, H., Mombelli, A., Gmur, R., Mathey-Dinc, S. & Lang, N. P. (1992) Periodontal pathogens in the shallow pockets of immigrants from developing countries. Oral Microbiology & Immunology 7, 267-272. Mooney, J., Adonogianaki, E., Riggio, M. P., Takahashi, K., Haerian, A. & Kinane, D. F. (1995) Initial serum antibody titer to Porphyromonas gingivalis influences development of antibody avidity and success of therapy for chronic periodontitis. Infection & Immunity 63, 3411-3416. Smith, G. L., Socransky, S. S. & Smith, C. M. (1989 Rapid method for the purification of DNA from subgingival microorganisms. Oral Microbiology & Immunology 4, 47-51. Moore, W. E., Holdeman, L. V., Smibert, R. M., Cato, E. P., Burmeister, J. A., Palcanis, K. G. & Ranney, R. R. (1984) Bacteriology of experimental gingivitis in children. Infection & Immunity 46, 1-6. Haffajee, A. D. & Socransky, S. S. (1994) Microbial etiological agents of destructive periodontal diseases. Periodontology 2000 5, 78-111. Tanner, A. C. R., Listgarten, M. A., Ebersole, J. L. & Strzempko, M. N. (1986) Bacteroides forsythus sp. nov., a slow growing fusiform Bacteroides sp, from the human oral cavity. International Journal of Systematic Bacteriology 36, 213-221. Tanner, A., Bouldin, H. D. & Maiden, M. F. (1989) Newly delineated periodontal pathogens with special reference to Selenomonas species. Infection 17, 182-187. Kononen, E., Asikainen, S., Saarela, M., Karjalainen, J. & Jousimies-Somer, H. (1994) The oral gram-negative anaerobic microflora in young children: longitudinal changes from edentulous to dentate mouth. Oral Microbiology & Immunology 9, 136-141. Moore, L. V. H., Johnson, J. L. & Moore, W. E. C. (1987) Selenomonas noxia sp. nov., Selenomonas frueggeii sp. nov., Selenomonas infelix sp. nov., Selenomonas dianae sp. nov., and Selenomonas artemidis sp. nov., from the human gingival crevice. International Journal of Systematic Bacteriology 36, 271-280. Beck, J. D. & Koch, G. G. (1994) Characteristics of older adults experiencing periodontal attachment loss as gingival recession or probing depth. Journal of Periodontal Research 29, 290-298. Machtei, E. E., Christersson, L. A., Zambon, J. J., Hausmann, E., Grossi, S. G., Dunford, R. & Genco, R.J. (1993) Alternative methods for screening periodontal disease in adults. Journal of Clinical Periodontology 20, 81-87. Grossi, S. G., Genco, R. J., Machtei, E. E., Ho, A. W., Koch, G., Dunford, R., Zambon, J. J. & Hausmann, E. (1995) Assessment of risk for periodontal disease. II. Risk indicators for alveolar bone loss. Journal of Periodontology 66, 23-29. Lai, C. H., Oshima, K., Slots, J. & Listgarten, M. A. (1992) Wolinella recta in adult gingivitis and periodontitis. Journal of Periodontal Research 27, 8-14. Wade, W. G., Gray, A. R., Absi, E. G. & Barker, G. R. (1991) Predominant cultivable fiora in pericoronitis. Oral Microbiology & Immunology 6, 310-312. Haffajee, A. D, Socransky, S. S., Smith, C & Dibart, S. (1991) Relation of baseline microbial parameters to future periodontal attachment loss. Journal of Clinical Periodontology 18, 744-750. Haffajee, A. D, Socransky, S. S., and Goodson, J. M. (1983b) Comparison of different data analyses for detecting changes in attachment level. Journal of Clinical Periodontology 10, 298-310. Lai, C. H., Listgarten, M. A., Shirakawa, M. & Slots, J. (1987) Bacteriodes forsythus in adult gingivitis and periodontitis. Oral Microbiology & Immunology 2, 152-157. Sneath, P. H. A. & Sokal, R. R. (1973) Numerical taxonomy. The principles and practice of numerical classification. Freeman, San Francisco . Newman, M. G., Grinenco, V. Weiner, M., Angel, I., Karge, H. & Nisengard, R. (1978) Predominant microbiota associated with periodontal health in the aged. Journal of Periodontology 49, 553-559. Engler-Blum, G., Meier, M., Frank, J. & Muller, G. A. (1993) Reduction of background problems in nonradioactivc northern and Southern blot analyses enables higher sensitivity than 32P-based hybridizations. Analytical Biochemistry 210, 235-244. Dzink, J. L., Socransky, S. S. & Haffajee, A. D. (1988) The predominant cultivable microbiota of active and inactive lesions of destructive periodontal diseases. Journal of Clinical Periodontology 15, 316-323. Bergstrom, J. & Preber, H. (1994) Tobacco use as a risk factor. Journal of Periodontology 65, 545-50. Joshipura, K. J., Kent, R. L. & DePaola, P.F. (1994) Gingival recession: intra-oral distribution and associated factors. Journal of Periodontology 65, 864-871 [see comments]. Tanner, A. & Bouldin, H. (1989) The microbiota of early periodontitis lesions in adults. Journal of Clinical Periodontology 16, 467-471. Saarela, M., Von Troil-Linden, B., Torkko, H., Stucki, A. M., Alaluusua, S., Jousimies-Somer, H. & Asikainen, S. (1993) Transmission of oral bacterial species between spouses. Oral Microbiology & Immunology 8, 349-354. Gunaratnam, M., Smith, G. L., Socransky, S. S., Smith, C. M. & Haffajee, A. D. (1992) Enumeration of subgingival species on primary isolation plates using colony lifts. Oral Microbiology & Inmmunology 7, 14-18. Dahlen, G., Manji, F., Baelum, V & Fejerskov, O. (1992) Putative periodontopathogens in "diseased" and "non-diseased" persons exhibiting poor oral hygiene. Journal of Clinical Periodontology 19, 35-42. Moore, W. E. C. & Moore, L. V. H. (1994) The bacteria of periodontal diseases. Periodontology 2000 5, 66-77. Riviere, G. R., Smith, K. S., Tzagaroulaki, E., Kay, S. L., Zhu, X., DeRouen, T. A. & Adams, D. F. (1996) Periodontal status and detection frequency of bacteria at sites of periodontal health and gingivitis. Journal of Periodontology 67, 109-115. Alaluusua, S., Asikainen, S. & Lai, C.H. (1991) Intrafamilial transmission of Actinobacillus actinomycetemcomitans. Journal of Periodontology 62, 207-210. Maiden, M. F. J., Tanner, A. & Macuch, P. (1996) Rapid characterization of periodontal bacterial isolates by using fluorogenic substrate tests. Journal of Clinical Microbiology 34, 376-384. Slots, J. (1977) Microflora in the healthy gingival sulcus in man, Scandinavian Journal of Denial Research 85, 247-254. Maiden, M. F., Tanner, A. & Moore, W. E. (1992) Identification of Selenomonas species by whole-genomic DNA probes, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, biochemical tests and cellular fatty acid analysis. Oral Microbiology & Immunology 7, 7-13. Slots, J., Moenbo, D, Langebaek, J. & Erandsen, A. (1978) Microbiota of gingivitis in man, Scandinavian Journal of Dental Research 86, 174-181. Kononen, E., Saarela, M., Karjalainen, J., Jousimies-Somer, H., Alaluusua, S. & Asikainen, S. (1994) Transmission of oral Prevotella melaninogenica between a mother and her young child. Oral Microbiology & Immunology 9, 310-314. Syed, S. A. & Loesche, W. J. (1978) Bacteriology of human experimental gingivitis: effect of plaque age. Infection & Immunity 21, 821-829. Haffajee, A. D., Socransky, S. S. & Goodson, J. M. (1992) Subgingival temperature (II). Relation to future periodontal attachment loss. Journal of Clinical Periodontology 19, 409-416. Socransky, S. S., Smith, C, Martin, L., Paster, B. J., Dewhirst, F. E. & Levin, A. E. (1994) "Checkerboard" DNA-DNA hybridization. BioTechniques 17, 788-793. Grossi, S. G., Zambon, J. J., Ho, A. W. Koch, G., Dunford, R. G., Machtei, E. E., Norderyd, O. M. & Genco, R. J. (1994) Assessment of risk for periodontal disease. I. Risk indicators for attachment loss. Journal of Periodontology 65, 260-267. Haffajee, A. D., Socransky, S. S. & Goodson, J. M. (1983a) Clinical parameters as predictors of destructive periodontal disease activity. Journal of Clinical Peridontology 10, 257-265. Moore, L. V. Moore, W. E., Cato, E. P., Smibert, R. M., Burmeister, J. A., Best, A. M. & Ranney, R. R. (1987) Bacteriology of human gingivitis. Journal of Denial Research 66, 989-995. Socransky, S. S., Haffajee, A. D., Dzink, J. L. & Hillman, J. D. (1988) Associations between microbial species in subgingival plaque samples. Oral Microbiology & Immunology 3, 1-7. 1987; 36 1993; 8 1991; 18 1987; 2 1989; 4 1982; 38 1988; 15 1993; 20 1986; 36 1984; 46 1983a; 10 1994; 00 1992; 19 1977; 85 1973 1994; 29 1991 1996; 31 1994; 65 1996; 34 1991; 6 1994; 9 1992; 7 1995; 63 1987; 66 1983b; 10 1988; 3 1978; 21 1978; 86 1995; 66 1991; 62 1978; 49 1992; 27 1994; 17 1985; 12 1989; 16 1994; 5 1989 1996; 67 1989; 17 1993; 210 Bergstrom J. (e_1_2_1_4_1) 1994; 65 Slots J. (e_1_2_1_40_1) 1978; 86 Loesche W. J. (e_1_2_1_24_1) 1978; 21 Moore W. E. (e_1_2_1_32_1) 1982; 38 Moore W. E. (e_1_2_1_33_1) 1984; 46 e_1_2_1_20_1 e_1_2_1_41_1 e_1_2_1_22_1 e_1_2_1_43_1 e_1_2_1_28_1 e_1_2_1_49_1 e_1_2_1_26_1 e_1_2_1_47_1 e_1_2_1_31_1 e_1_2_1_8_1 e_1_2_1_6_1 e_1_2_1_35_1 e_1_2_1_50_1 e_1_2_1_10_1 e_1_2_1_52_1 e_1_2_1_2_1 e_1_2_1_16_1 e_1_2_1_14_1 e_1_2_1_37_1 e_1_2_1_18_1 Socransky S. S. (e_1_2_1_44_1) 1994; 17 Tanner A. (e_1_2_1_46_1) 1991 Slots J. (e_1_2_1_39_1) 1977; 85 Haber J. (e_1_2_1_12_1) 1994; 00 Mooney J. (e_1_2_1_29_1) 1995; 63 e_1_2_1_23_1 e_1_2_1_21_1 e_1_2_1_25_1 e_1_2_1_48_1 Sneath P. H. A. (e_1_2_1_42_1) 1973 e_1_2_1_7_1 Syed S. A. (e_1_2_1_45_1) 1978; 21 e_1_2_1_30_1 e_1_2_1_5_1 e_1_2_1_3_1 e_1_2_1_13_1 e_1_2_1_34_1 e_1_2_1_51_1 e_1_2_1_11_1 e_1_2_1_17_1 e_1_2_1_38_1 Maiden M. F. J. (e_1_2_1_27_1) 1996; 34 e_1_2_1_15_1 e_1_2_1_36_1 e_1_2_1_9_1 e_1_2_1_19_1
References_xml	– reference: McNabb, H., Mombelli, A., Gmur, R., Mathey-Dinc, S. & Lang, N. P. (1992) Periodontal pathogens in the shallow pockets of immigrants from developing countries. Oral Microbiology & Immunology 7, 267-272. – reference: Haffajee, A. D, Socransky, S. S., and Goodson, J. M. (1983b) Comparison of different data analyses for detecting changes in attachment level. Journal of Clinical Periodontology 10, 298-310. – reference: Wade, W. G., Gray, A. R., Absi, E. G. & Barker, G. R. (1991) Predominant cultivable fiora in pericoronitis. Oral Microbiology & Immunology 6, 310-312. – reference: Loesche, W. J. & Syed, S. A. (1978) Bacteriology of human experimental gingivitis: effect of plaque and gingivitis score. Infection & Immunity 21, 830-839. – reference: Lai, C. H., Listgarten, M. A., Shirakawa, M. & Slots, J. (1987) Bacteriodes forsythus in adult gingivitis and periodontitis. Oral Microbiology & Immunology 2, 152-157. – reference: Saarela, M., Von Troil-Linden, B., Torkko, H., Stucki, A. M., Alaluusua, S., Jousimies-Somer, H. & Asikainen, S. (1993) Transmission of oral bacterial species between spouses. Oral Microbiology & Immunology 8, 349-354. – reference: Tanner, A., Bouldin, H. D. & Maiden, M. F. (1989) Newly delineated periodontal pathogens with special reference to Selenomonas species. Infection 17, 182-187. – reference: Riviere, G. R., Smith, K. S., Tzagaroulaki, E., Kay, S. L., Zhu, X., DeRouen, T. A. & Adams, D. F. (1996) Periodontal status and detection frequency of bacteria at sites of periodontal health and gingivitis. Journal of Periodontology 67, 109-115. – reference: Newman, M. G., Grinenco, V. Weiner, M., Angel, I., Karge, H. & Nisengard, R. (1978) Predominant microbiota associated with periodontal health in the aged. Journal of Periodontology 49, 553-559. – reference: Gmur, R., Strub, J. R. & Guggenheim, B. (1989) Prevalence of Bacteroides forsythus and Bacteroides gingivalis in subgingival plaque of prosthodontically treated patients on short recall. Journal of Periodontal Research, 113-120. – reference: Gunaratnam, M., Smith, G. L., Socransky, S. S., Smith, C. M. & Haffajee, A. D. (1992) Enumeration of subgingival species on primary isolation plates using colony lifts. Oral Microbiology & Inmmunology 7, 14-18. – reference: Moore, W. E., Holdeman, L. V. Smibert, R. M., Good, I. J., Burmeister, J. A., Palcanis, K. G. & Ranney, R. R. (1982) Bacteriology of experimental gingivitis in young adult humans. Infection & Immunity 38, 651-667. – reference: Tanner, A., Kent, R., Maiden, M. F. J. & Taubman, M. A. (1996) Clinical, microbiological and immunological profile of health, gingivitis and putative active periodontal subjects. Journal of Periodontal Research 31, 195-204. – reference: Socransky, S. S., Smith, C, Martin, L., Paster, B. J., Dewhirst, F. E. & Levin, A. E. (1994) "Checkerboard" DNA-DNA hybridization. BioTechniques 17, 788-793. – reference: Lai, C. H., Oshima, K., Slots, J. & Listgarten, M. A. (1992) Wolinella recta in adult gingivitis and periodontitis. Journal of Periodontal Research 27, 8-14. – reference: Grossi, S. G., Zambon, J. J., Ho, A. W. Koch, G., Dunford, R. G., Machtei, E. E., Norderyd, O. M. & Genco, R. J. (1994) Assessment of risk for periodontal disease. I. Risk indicators for attachment loss. Journal of Periodontology 65, 260-267. – reference: Moore, L. V. H., Johnson, J. L. & Moore, W. E. C. (1987) Selenomonas noxia sp. nov., Selenomonas frueggeii sp. nov., Selenomonas infelix sp. nov., Selenomonas dianae sp. nov., and Selenomonas artemidis sp. nov., from the human gingival crevice. International Journal of Systematic Bacteriology 36, 271-280. – reference: Moore, W. E. C. & Moore, L. V. H. (1994) The bacteria of periodontal diseases. Periodontology 2000 5, 66-77. – reference: Joshipura, K. J., Kent, R. L. & DePaola, P.F. (1994) Gingival recession: intra-oral distribution and associated factors. Journal of Periodontology 65, 864-871 [see comments]. – reference: Haffajee, A. D., Socransky, S. S. & Goodson, J. M. (1983a) Clinical parameters as predictors of destructive periodontal disease activity. Journal of Clinical Peridontology 10, 257-265. – reference: Dzink, J. L., Socransky, S. S. & Haffajee, A. D. (1988) The predominant cultivable microbiota of active and inactive lesions of destructive periodontal diseases. Journal of Clinical Periodontology 15, 316-323. – reference: Syed, S. A. & Loesche, W. J. (1978) Bacteriology of human experimental gingivitis: effect of plaque age. Infection & Immunity 21, 821-829. – reference: Kononen, E., Asikainen, S., Saarela, M., Karjalainen, J. & Jousimies-Somer, H. (1994) The oral gram-negative anaerobic microflora in young children: longitudinal changes from edentulous to dentate mouth. Oral Microbiology & Immunology 9, 136-141. – reference: Haffajee, A. D., Socransky, S. S. & Goodson, J. M. (1992) Subgingival temperature (II). Relation to future periodontal attachment loss. Journal of Clinical Periodontology 19, 409-416. – reference: Beck, J. D. & Koch, G. G. (1994) Characteristics of older adults experiencing periodontal attachment loss as gingival recession or probing depth. Journal of Periodontal Research 29, 290-298. – reference: Sneath, P. H. A. & Sokal, R. R. (1973) Numerical taxonomy. The principles and practice of numerical classification. Freeman, San Francisco . – reference: Maiden, M. F., Tanner, A. & Moore, W. E. (1992) Identification of Selenomonas species by whole-genomic DNA probes, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, biochemical tests and cellular fatty acid analysis. Oral Microbiology & Immunology 7, 7-13. – reference: Moore, L. V. Moore, W. E., Cato, E. P., Smibert, R. M., Burmeister, J. A., Best, A. M. & Ranney, R. R. (1987) Bacteriology of human gingivitis. 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Infection & Immunity 63, 3411-3416. – reference: Socransky, S. S., Haffajee, A. D., Dzink, J. L. & Hillman, J. D. (1988) Associations between microbial species in subgingival plaque samples. Oral Microbiology & Immunology 3, 1-7. – reference: Haffajee, A. D. & Socransky, S. S. (1994) Microbial etiological agents of destructive periodontal diseases. Periodontology 2000 5, 78-111. – reference: Slots, J., Moenbo, D, Langebaek, J. & Erandsen, A. (1978) Microbiota of gingivitis in man, Scandinavian Journal of Dental Research 86, 174-181. – reference: Bergstrom, J. & Preber, H. (1994) Tobacco use as a risk factor. Journal of Periodontology 65, 545-50. – reference: Maiden, M. F. J., Tanner, A. & Macuch, P. (1996) Rapid characterization of periodontal bacterial isolates by using fluorogenic substrate tests. Journal of Clinical Microbiology 34, 376-384. – reference: van Steenbergen, T. J., Petit, M. D., Scholte, L. H., Van der Velden, U. & de Graaff, J. 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Snippet	. This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe,... This study compared the subgingival microbiota in periodontal health, gingivitis and initial periodontitis using predominant culture and a DNA probe,...
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SubjectTerms	Adult Bacteroidaceae - isolation & purification Bacteroidaceae - pathogenicity Bacteroides - isolation & purification Bacteroides - pathogenicity Campylobacter - isolation & purification Campylobacter - pathogenicity Cluster Analysis Colony Count, Microbial Dental Plaque - metabolism Disease Progression DNA Probes DNA, Bacterial - analysis Female Gingiva - microbiology Gingival Recession - microbiology Gingivitis - microbiology Gram-Negative Bacteria - isolation & purification Gram-Positive Bacteria - isolation & purification Humans initial periodontitis Longitudinal Studies Male microbiology microbiota Middle Aged Periodontal Attachment Loss - microbiology periodontal disease Periodontitis - microbiology Statistics, Nonparametric
Title	Microbiota of health, gingivitis, and initial periodontitis
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