<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd">
<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="healthcare" lang="en"><front><journal-meta><journal-id journal-id-type="publisher">IJCRR</journal-id><journal-id journal-id-type="nlm-ta">I Journ Cur Res Re</journal-id><journal-title-group><journal-title>International Journal of Current Research and Review</journal-title><abbrev-journal-title abbrev-type="pubmed">I Journ Cur Res Re</abbrev-journal-title></journal-title-group><issn pub-type="ppub">2231-2196</issn><issn pub-type="opub">0975-5241</issn><publisher><publisher-name>Radiance Research Academy</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1745</article-id><article-id pub-id-type="doi"/><article-id pub-id-type="doi-url"/><article-categories><subj-group subj-group-type="heading"><subject>Healthcare</subject></subj-group></article-categories><title-group><article-title>QUANTIFICATION OF SUBGINGIVAL MICROFLORA IN A PERI IMPLANTITIS PATIENT USING REAL TIME POLYMERASE CHAIN REACTION TECHNIQUE - A PILOT STUDY&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Prakash</surname><given-names>PSG</given-names></name></contrib><contrib contrib-type="author"><name><surname>Victor</surname><given-names>D.J.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Vaishnavi</surname><given-names>S.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Abraham</surname><given-names>Ponsekar A.</given-names></name></contrib></contrib-group><volume>)</volume><issue/><fpage>6</fpage><lpage>19</lpage><permissions><copyright-statement>This article is copyright of Popeye Publishing, 2009</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p></license></permissions><abstract><p>Aim and Objective: Peri-implantitis is a chronic progressive marginal infection which is defined as an inflammatory reaction affecting the tissues surrounding osseointegrated dental implants resulting in loss of supporting bone. The microflora of patients with implants who are edentulous mainly consists of gram positive facultative cocci and non motile rods. Predominantly Streptococcus sanguis, Streptococcus mitis are found in a healthy, stable implant whereas motile rods, Spirochetes, Fusiforms and filaments are infrequently found. Microbiota around the failing implant in edentulous patients usually consists of gram negative anaerobic rods. In partially edentulous patients, peri implant microorganisms in a stable implant majorly consists of motile rods, Spirochetes and cocci. In a failing implant in partially edentulous patients high proportions of P.micros, P.intermedia, C.rectus and Fusobacterium species were observed (Alcoforado et al in 1994). The concept that the composition of subgingival microflora around implants in partially edentulous patients is said to be resultant of composition of flora around the teeth. Based on this principle we set out to identify the presence of putative periodontal pathogens on teeth in a predominantly edentulous arch with a metallic coping with periodontitis and a site in the same mouth with peri__ampersandsignnbsp;implantitis. Materials and Method: Subgingival plaque samples were collected from a partially edentulous patient using a paper point from the periimplantitis lesion with a probing depth of 8-9mm and&#13;
a tooth with deepest pocket with a probing depth of 6mm and we analyzed the five putative periodontal pathogens namely, P.gingivalis, P.intermedia, P.nigrecens, T.denticola and T.forcythia using Real Time Polymerised Chain Reaction (RTPCR) technique. Results: P.Gingivalis and P.Intermedia , P.Nigrecens had a 3 fold increase and T.Denticola had 1 fold increase when compared to the periodontitis ( teeth) site, and T.Forsythia was found in trace amounts at the periimplantitis site and was completely absent at the periodontitis( teeth) site.&#13;
</p></abstract><kwd-group><kwd>Implants</kwd><kwd> Periimplantitis</kwd><kwd> Periimplant microflora</kwd><kwd> Ball abutments</kwd><kwd> Over denture.</kwd></kwd-group></article-meta></front></article>
