Hp. Muller et al., MICROBIAL ECOLOGY OF ACTINOBACILLUS-ACTINOMYCETEMCOMITANS, EIKENELLA-CORRODENS AND CAPNOCYTOPHAGA SPP. IN ADULT PERIODONTITIS, Journal of Periodontal Research, 32(6), 1997, pp. 530-542
Information an intraoral distribution of putative periodontal pathogen
s might be essential for controlling different forms of periodontal di
sease. Colonization may be either promoted or impeded by other bacteri
a competing in the subgingival ecosystem. In recent investigations mic
robial associations between dental organisms have been determined in a
multitude of subgingival plaque samples within multiple patients and
described by odds ratios, In most circumstances without taking into ac
count the correlated structure of the observations within a single ind
ividual. The present investigation had 3 major objectives: (i) to desc
ribe the intraoral distribution of some facultatively anaerobic, Gram-
negative rods, i.e. Actinobacillus actinomycetemcomitans, Eikenella co
rrodens-like organisms and Capnocytophaga spp., in a multitude of subg
ingival and extracrevicular samples of 10 adult subjects with A. actin
omycetemcomitans-associated periodontitis; (ii) to analyse possible in
consistencies of microbial associations between these periodontal orga
nisms; and (iii) to determine factors increasing the likelihood of iso
lating these bacteria in a given subgingival site by employing General
ized Estimation Equation (GEE) methods. Clinical examinations were car
ried out at 6 sites of every tooth present. In each subject. 13 extrac
revicular (2 cheek mucosa, 3 tongue, 4 gingival, 2 tonsillar samples,
1 palatinal, 1 saliva sample) and between 22 and 44 subgingival sample
s from deepest sites of every tooth present (n=296) were selectively c
ultivated for A. actinomycetemcomitans, E. corrodens and Capnocytophag
a spp. In extracrevicular material, A. actinomycetemcomitans, Capnocyt
ophaga spp. and E. corrodens were isolated in 9, 10 and 6 patients, an
d from 65, 82 and 15% samples, respectively. The organisms were recove
red from 51, 62 and 27% subgingival plaque samples, respectively. Hete
rogeneity tests did not reveal significant inconsistencies of microbia
l associations between bacteria in subgingival plaque. Mantel-Haenszel
's odds ratios ranged between 2.0 for A. actinomycetemcomitans and Cap
nocytophaga spp. and 18.7 for Capnocytophaga spp. and E. corrodens. An
exchangeable working dependence structure was employed in the GEE app
roach. The odds of isolating A. actinomycetemcomitans was increased by
factor 3.7 in 4-6 mm deep pockets, and 9.5 in greater than or equal t
o 7 mm deep pockets. The odds of presence of E. corrodens was increase
d by factor 10.8 in the case of presence of Capnocytophaga spp. and 2.
1 in the case of presence of A. actinomycetemcomitans. Capnocytophaga
spp. were associated with bleeding on probing and molar sites. Presenc
e of E. corrodens was associated with clinical attachment loss but not
periodontal probing depth. Results of the present study indicated an
association of A. actinomycetemcomitans with periodontal pathology. Wh
ereas this organism and Cagnocytophagae were widely distributed in ext
racrevicular ecosystems of the mouth, E. corrodens only occasionally a
ppeared in saliva or on mucous membranes of the oral cavity. In genera
l, GEE methods seem to allow to determine factors associated with the
presence of periodontal organisms in a multivariate approach and consi
dering the correlated structure of the data.