Real time detection and quantification of Epstein Barr virus in different grades of oral gingivitis and periodontitis patients.


Journal

Journal of experimental therapeutics & oncology
ISSN: 1359-4117
Titre abrégé: J Exp Ther Oncol
Pays: United States
ID NLM: 9604933

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 21 06 2018
accepted: 24 08 2018
entrez: 19 1 2019
pubmed: 19 1 2019
medline: 15 8 2019
Statut: ppublish

Résumé

Periodontal diseases are of microbial etiology and are globally causing loss of teeth in adult population. Many severe oral diseases have been recently associated to Herpes viruses, of which Epstein Barr Virus (EBV) and human cytomegalovirus (HCMV) have been indicated in the etiology of periodontal diseases. The purpose of the study was to compare the effect of EBV in different types of periodontal diseases namely acute gingivitis, chronic gingivitis, acute and chronic, localized and generalized aggressive (juvenile) periodontitis and apical periodontitis. 70 individuals were included in this study. Supragingival plaque and plaque from two deepest sites of the periodontal pockets were collected then stored at 70° c and prepared for nucleic acid extraction. For EBV detection, DNA were extracted from the plaque samples with the QIAamp DNA mini kit. Q-PCR was performed by targeting the non-polymorphic Epstein-Barr nuclear antigen-1 (EBNA-1) gene using Corbett Research 6000 Q-PCR instrument and Rotor gene 6000 software. Overall prevalence of EBV in the disease group was 60% (27/45 patients) as compared to only 8% (4/25 people) in the normal population. The mean copy number of EBV DNA was found to be significantly higher in periodontitis (2234 ± 1811.34) when compared to gingivitis (554 ± 537.64, p = .001) and normal patients (370 ± 161.03, p < .001). Here, we found that the prevalence of EBV as well as copy number of EBV was significantly higher in periodontitis patients as compared to gingivitis patients or normal population.

Sections du résumé

BACKGROUND BACKGROUND
Periodontal diseases are of microbial etiology and are globally causing loss of teeth in adult population. Many severe oral diseases have been recently associated to Herpes viruses, of which Epstein Barr Virus (EBV) and human cytomegalovirus (HCMV) have been indicated in the etiology of periodontal diseases.
AIM OBJECTIVE
The purpose of the study was to compare the effect of EBV in different types of periodontal diseases namely acute gingivitis, chronic gingivitis, acute and chronic, localized and generalized aggressive (juvenile) periodontitis and apical periodontitis.
MATERIAL AND METHOD METHODS
70 individuals were included in this study. Supragingival plaque and plaque from two deepest sites of the periodontal pockets were collected then stored at 70° c and prepared for nucleic acid extraction. For EBV detection, DNA were extracted from the plaque samples with the QIAamp DNA mini kit. Q-PCR was performed by targeting the non-polymorphic Epstein-Barr nuclear antigen-1 (EBNA-1) gene using Corbett Research 6000 Q-PCR instrument and Rotor gene 6000 software.
RESULTS RESULTS
Overall prevalence of EBV in the disease group was 60% (27/45 patients) as compared to only 8% (4/25 people) in the normal population. The mean copy number of EBV DNA was found to be significantly higher in periodontitis (2234 ± 1811.34) when compared to gingivitis (554 ± 537.64, p = .001) and normal patients (370 ± 161.03, p < .001).
CONCLUSION CONCLUSIONS
Here, we found that the prevalence of EBV as well as copy number of EBV was significantly higher in periodontitis patients as compared to gingivitis patients or normal population.

Identifiants

pubmed: 30658021

Types de publication

Journal Article

Langues

eng

Pagination

9-14

Informations de copyright

© 2018 Old City Publishing, Inc.

Auteurs

Apurva K Srivastava (AK)

Department of Pathology & Microbiology, Saraswati Dental & Medical College, Lucknow - 227105, India.

Sanket Shukla (S)

Department of Microbiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow - 226014, India.

Priya Srivastava (P)

Department of Microbiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow - 226014, India.

T N Dhole (TN)

Department of Microbiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow - 226014, India.

Meghanand T Nayak (MT)

Department of Oral Pathology and Microbiology, Teerthanker Mahaveer Dental College & Research Centre, Moradabad - 244001, U.P, India.

Anjali Nayak (A)

Department of Oral Medicine and Radiology, Teerthanker Mahaveer Dental College & Research Centre, Moradabad - 244001, U.P, India.

Asha Mathur (A)

Department of Pathology & Microbiology, Saraswati Dental & Medical College, Lucknow - 227105, India.

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