Journal of Endodontics
Volume 26, Issue 4 , Pages 217-220, April 2000

Whole Genomic DNA Probe for Detection of Porphyromonas endodontalis

  • R. Nissan, DMD

      Affiliations

    • Dr. Nissan is assistant professor, Department of Endodontology, Temple University Dental School, Philadelphia, PA
    • Corresponding Author InformationAddress requests for reprints to Dr. Roni Nissan, Department of Endodontology, Temple University Dental School, 3223 North Broad Street, Philadelphia, PA 19140-5096
  • ,
  • S.R. Makkar, DDS

      Affiliations

    • Dr. Makkar was an endodontic resident in the Department of Endodontology, Temple University Dental School, and is now in endodontic private practice in North Boston, MA
  • ,
  • M.N. Sela, DMD, PhD

      Affiliations

    • Dr. Sela is professor and chairman, Department of Oral Biology, School of Dentistry, Hebrew University, Jerusalem, Israel
  • ,
  • R. Stevens, DDS, MS

      Affiliations

    • Dr. Stevens is professor and chairman, Department of Endodontology, Temple University Dental School, Philadelphia, PA

The purpose of the present study was to develop a DNA probe for Porphyromonas endodontalis. Pure cultures of P. endodontalis were grown in TYP medium, in an anaerobic chamber. DNA was extracted from the P. endodontalis and labeled using the Genius System by Boehringer Mannheim. The labeled P. endodontalis DNA was used in dot-blot hybridization reactions with homologous (P. endodontalis) and unrelated bacterial samples. To determine specificity, strains of 40 other oral bacterial species (e.g. Porphyromonas gingivalis, Porphyromonas asaccharolytica, and Prevotella intermedia) were spotted and reacted with the P. endodontalis DNA probe. None of the panel of 40 oral bacteria hybridized with the P. endodontalis probe, whereas the blot of the homologous organism showed a strong positive reaction. To determine the sensitivity of the probe, dilutions of a P. endodontalis suspension of known concentration were blotted onto a nylon membrane and reacted with the probe. The results of our investigation indicate that the DNA probe that we have prepared specifically detects only P. endodontalis and can detect at least 3 × 104 cells.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 20.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 This study was supported in part by the Faculty Incentive Award #466 from Temple University, Philadelphia, PA.

PII: S0099-2399(05)60957-0

doi:10.1097/00004770-200004000-00004

Journal of Endodontics
Volume 26, Issue 4 , Pages 217-220, April 2000