Literature DB >> 2469776

Synthetic oligodeoxynucleotide probes for the rapid detection of bacteria associated with human periodontitis.

P J Chuba1, K Pelz, G Krekeler, T S de Isele, U Göbel.   

Abstract

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.

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Year:  1988        PMID: 2469776     DOI: 10.1099/00221287-134-7-1931

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  12 in total

1.  Phenotypic and genotypic analysis of Borrelia burgdorferi isolates from various sources.

Authors:  T Adam; G S Gassmann; C Rasiah; U B Göbel
Journal:  Infect Immun       Date:  1991-08       Impact factor: 3.441

2.  Rapid identification of Actinobacillus actinomycetemcomitans, Haemophilus aphrophilus, and Haemophilus paraphrophilus by restriction enzyme analysis of PCR-amplified 16S rRNA genes.

Authors:  M P Riggio; A Lennon
Journal:  J Clin Microbiol       Date:  1997-06       Impact factor: 5.948

3.  Multiplex PCR using conserved and species-specific 16S rRNA gene primers for simultaneous detection of Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis.

Authors:  S D Tran; J D Rudney
Journal:  J Clin Microbiol       Date:  1996-11       Impact factor: 5.948

4.  Serodiagnosis of Porphyromonas gingivalis infection by immunoblot analysis with recombinant collagenase.

Authors:  M Wittstock; T F Flemmig; H Schmidt; R Mutters; H Karch
Journal:  J Clin Microbiol       Date:  1996-10       Impact factor: 5.948

5.  Diversity of cultivable and uncultivable oral spirochetes from a patient with severe destructive periodontitis.

Authors:  B K Choi; B J Paster; F E Dewhirst; U B Göbel
Journal:  Infect Immun       Date:  1994-05       Impact factor: 3.441

6.  Identification of Bacteroides forsythus in subgingival plaque from patients with advanced periodontitis.

Authors:  H Gersdorf; A Meissner; K Pelz; G Krekeler; U B Göbel
Journal:  J Clin Microbiol       Date:  1993-04       Impact factor: 5.948

7.  Age and prevalence of Porphyromonas gingivalis in children.

Authors:  D L McClellan; A L Griffen; E J Leys
Journal:  J Clin Microbiol       Date:  1996-08       Impact factor: 5.948

8.  Filifactor alocis--involvement in periodontal biofilms.

Authors:  Sebastian Schlafer; Birgit Riep; Ann L Griffen; Annett Petrich; Julia Hübner; Moritz Berning; Anton Friedmann; Ulf B Göbel; Annette Moter
Journal:  BMC Microbiol       Date:  2010-03-01       Impact factor: 3.605

9.  Detection and strain identification of Actinobacillus actinomycetemcomitans by nested PCR.

Authors:  E J Leys; A L Griffen; S J Strong; P A Fuerst
Journal:  J Clin Microbiol       Date:  1994-05       Impact factor: 5.948

10.  Designation of Streptomycete 16S and 23S rRNA-based target regions for oligonucleotide probes.

Authors:  E Stackebrandt; D Witt; C Kemmerling; R Kroppenstedt; W Liesack
Journal:  Appl Environ Microbiol       Date:  1991-05       Impact factor: 4.792

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