Taxonom ic relationships of the

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Both treatment modalities led to an improvement of the clinical parameters and a temporary reduction of the microflora at implants with mucositis, but without significant inter-group differences after 8 months.

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The phylogenetic position and various genotypic, chemotaxonomic, and classical phenotypic characteristics of 21 gram-negative avian isolates were studied. These strains constitute a genotypically homogeneous taxon in rRNA superfamily V, as shown by DNA-rRNA hybridization data. Determination of the 16s rRNA sequence of this taxon revealed its detailed position within the "flavobacter" subgroup of the "flavobacter-bacteroides" phylum as described by Gherna and Woese (R. Gherna and C. R. Woese, Syst. Apple Microbiol. 15513-521, 1992). This new taxon is only distantly related to other members of the "flavobacter-bacteroides" phylum and is therefore given separate generic status. The DNA-DNA binding values for members of this taxon, for which we propose the name Ornithobacterium rhinotracheale, confirmed that all of the strains are highly interrelated (DNA-DNA binding values greater than 90% were measured). The G+C contents of members of this taxon are between 37 and 39 mol%, An analysis of the cellular proteins and fatty acids and classical phenotypic characteristics allowed us to distinguish 0. rhinotracheafe from phenotypically similar taxa, such as Riemrelliz anatipestiyer and Capnocytophaga species. The respiratory quinone content (menaquinone 7) and carbohydrate pattern of 0 . rhinotracheale conform with the respiratory quinone contents and carbohydrate patterns of other members of rRNA superfamily V.In the past decade, we determined the protein and fatty acid profiles of a large number of avian isolates which could not be classified after primary identification tests were performed in veterinary laboratories. A total of 21 of these isolates had very similar profiles and differed clearly from all of the other strains investigated, including reference strains of well-known fowl pathogens. These 21 strains were isolated from the respiratory tracts of turkeys (10 strains), chickens (7 strains), rooks, (3 strains), and a partridge (1 strain). Clinical data were not available for all of these strains. However, most of the strains were associated with various respiratory tract infections, including tracheitis, pericarditis, sinusitis, airsacculitis, and pneumonia. Preliminary data on some of the chemotaxonomic characteristics of four strains have been described previously (36).We studied a wide range of taxonomic parameters, including genotypic, chemotaxonomic, and classical phenotypic parameters, in order to establish the phylogenetic affiliation and to comprehensively describe the new taxon, for which we propose the name Omithobacterium rhinotracheale. Special emphasis was given to the differentiation of 0. rhinotracheale, Riemerella anatipestifer, and Capnocytophaga species as these taxa share a number of phenotypic characteristics. * Corresponding author. Mailing address: Laboratorium voorMicrobiologie, Universiteit Gent, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium. Phone: 32-9-2645114. Fax: 32-9-2645346. MATERIALS AND METHODSIsolation of 0. rhinotracheale strains. Samples were inoculated onto media routinel...

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The purpose of this study was to determine the distribution of the putative periodontal pathogens Prevotella intermedia, Prevotella nigrescens, the three oral Capnocytophaga species (C. ochracea, C. sputigena, C. gingivalis), as well as Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans in plaque samples of periodontally healthy individuals. We chose a newly developed 16S rDNA directed Polymerase chain reaction (PCR) and a previously described dot‐blot hybridization assay to detect, differentiate, and quantify these bacteria directly in clinical samples. The subjects of these investigations were 66 sulcus fluid samples from 17 children (ages 3 to 5) attending a kindergarten, 48 sulcus fluid samples from 12 children (ages 9 and 10) from a primary school, and 25 subgingival plaque samples isolated from 6 different periodontally healthy dental students (ages 24 to 27). We were able to demonstrate the presence of P. nigrescens in 54 (kindergarten: 5; primary school: 33; students: 16) samples by PCR and quantified it by dot‐blot hybridization. In addition, we found C. ochracea in 12 (kindergarten: 2; primary school: 10) samples by PCR reaction only. The other tested bacterial species were absent by the methods used. Furthermore we confirmed the specificity of our P. nigrescens‐PCR in selected samples by enzyme electrophoresis. J Periodontol 1996;67:994–1003.