Synthetic Oligodeoxynucleotide Probes for the Rapid Detection of Bacteria Associated with Human Periodontitis

1 Institut für Medizinische Mikrobiologie und Hygiene der Universität Freiburg, Hermann Herder Strasse 11, D-7800 Freiburg, FRG 2 Zentrum für ZMK, Sektion Parodontalchirurgie, Hugstetter Strasse 55, D-7800 Freiburg, FRG ABSTRACT Summary: Analysis of the subgingival microflora has recently implicated...

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Veröffentlicht in:Journal of general microbiology 1988-07, Vol.134 (7), p.1931-1938
Hauptverfasser: Chuba, Paul J, Pelz, Klaus, Krekeler, Gisbert, De Isele, Teresa S, gobel, Ulf
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Sprache:eng
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Zusammenfassung:1 Institut für Medizinische Mikrobiologie und Hygiene der Universität Freiburg, Hermann Herder Strasse 11, D-7800 Freiburg, FRG 2 Zentrum für ZMK, Sektion Parodontalchirurgie, Hugstetter Strasse 55, D-7800 Freiburg, FRG ABSTRACT Summary: Analysis of the subgingival microflora has recently implicated Actinobacillus (Haemophilus) actinomycetemcomitans and several black Bacteroides species in the aetiology of juvenile, adult and rapidly progressing periodontitis. Rapid bacteriological diagnosis has been hampered by the slow growth and fastidious nature of these bacteria. To construct diagnostic probes, dideoxy sequencing of the 16S rRNA molecules from A. (H.) actinomycetemcomitans, Haemophilus aphrophilus, Bacteroides gingivalis, Bacteroides intermedius subgroup II, Bacteroides asaccharolyticus and several closely related species was performed. Next, oligodeoxynucleotides, complementary to defined regions of the 16S rRNA exhibiting considerable evolutionary divergence, were synthesized for use as molecular probes. In a dot-blot hybridization assay, all strains from each of the species for which probes were constructed were correctly identified, with a detection limit of less than 5 x 10 3 organisms. No cross-hybridization to closely related species (except for H. aphrophilus and Haemophilus paraphrophilus ) or contaminating bacteria was observed. Using a modified DNA/RNA hybridization technique, the detection could be performed in less than 12 h, as compared to 2-3 weeks using conventional bacteriological procedures.
ISSN:0022-1287
1350-0872
1465-2080
DOI:10.1099/00221287-134-7-1931