Literature DB >> 2088220

DNA probes in the diagnosis of periodontal microorganisms.

E D Savitt1, M W Keville, W J Peros.   

Abstract

The need for a rapid and sensitive microbiological assay has become necessary for both research and clinical diagnostic purposes. This need has become clear as a result of extensive documentation linking specific bacterial species and periodontal destruction. DNA probe technology provides both a sensitive and specific assay and alleviates the concern for transport of fastidious microorganisms. The DNA probe procedure includes (1) disruption of bacterial cells with denaturation of DNA, (2) immobilization of DNA onto a nitrocellulose filter, (3) blocking unbound nitrocellulose with non-specific DNA, (4) hybridization of the filter with 32P-labelled probe, (5) washing and detection of bound probe. At our laboratory, microbiological analysis with whole-genomic and cloned DNA probes has been used on thousands of plaque specimens in several large-scale research projects. In one study, levels (greater than or equal to 10(5)) of Actinobacillus actinomycetemcomitans were significantly higher in subjects under 21 yr than in subjects with adult periodontitis (over 21 yr old). In another study, the distribution of periodontal pathogens throughout the mouth was examined. High levels were selectively found at sites with probing depths of 5 mm or more and bleeding on probing, directing specimen collection to these sites. In contrast, random selection of sites for sampling was found to be a poor method for detecting high levels of pathogens. These data suggest appropriate sites for specimen collection for further research and diagnostic purposes.

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Year:  1990        PMID: 2088220     DOI: 10.1016/0003-9969(90)90147-3

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


  5 in total

Review 1.  Periodontal disease as a specific, albeit chronic, infection: diagnosis and treatment.

Authors:  W J Loesche; N S Grossman
Journal:  Clin Microbiol Rev       Date:  2001-10       Impact factor: 26.132

2.  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

3.  Immunomagnetic PCR and DNA probe for detection and identification of Porphyromonas gingivalis.

Authors:  R M Benkirane; E Guillot; C Mouton
Journal:  J Clin Microbiol       Date:  1995-11       Impact factor: 5.948

4.  Comparison of real-time PCR and culture for detection of Porphyromonas gingivalis in subgingival plaque samples.

Authors:  Khalil Boutaga; Arie Jan van Winkelhoff; Christina M J E Vandenbroucke-Grauls; Paul H M Savelkoul
Journal:  J Clin Microbiol       Date:  2003-11       Impact factor: 5.948

5.  Comparison of randomly cloned and whole genomic DNA probes for the detection of Porphyromonas gingivalis and Bacteroides forsythus.

Authors:  M Wong; J M DiRienzo; C H Lai; M A Listgarten
Journal:  J Periodontal Res       Date:  1996-01       Impact factor: 4.419

  5 in total

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