Advertisement

Human herpesvirus 7, Epstein–Barr virus and human cytomegalovirus in periodontal tissues of periodontally diseased and healthy subjects

Authors


  • Conflict of interest and source of funding statement
    The authors declare that they have no conflict of interests.
    This study was partly supported by a grant from the Ministero dell'Universitaè della Ricerca Scientifica e Tecnologica, Italy (MURST ex 60% 1999), by the Research Centre for the Study of Periodontal Diseases, University of Ferrara, Italy and by PRIN (ex 40%) and FAR (ex 60%).

Address:
Prof. Leonardo Trombelli
Research Center for the Study of Periodontal Diseases
University of Ferrara
Corso Giovecca 203
44100 Ferrara
Italy
E-mail: l.trombelli@unife.it

Abstract

Aims: To evaluate (i) the presence of human herpesvirus 7 (HHV-7), Epstein–Barr virus (EBV) and human cytomegalovirus (HCMV), and (ii) the transcription pattern of HHV-7 in gingival biopsies from patients affected by periodontitis (P) and periodontally healthy subjects (H).

Material and Methods: Thirty-seven subjects (P: n=24; H: n=13) were included. Each P patient contributed two gingival biopsies (representative of a clinically affected and non-affected site) and each H subject contributed one gingival biopsy. After DNA extraction, nested polymerase chain reaction was used to identify the viruses.

Results: HHV-7 was detected in 91.7% of P patients and in 61.5% of H subjects (p=0.02), EBV in 50.0% samples of P patients and 7.7% of H subjects (p=0.005) and HCMV only in one sample from H group. EBV was more frequently detected in biopsies from affected sites (50.0%) than from non-affected sites (16.7%) (p=0.008). HHV-7 transcription was detected in 15.4% of affected and 15.4% of non-affected sites.

Conclusions: The results indicate that (i) gingival tissues can be considered a potential reservoir for HHV-7; (ii) when present, HHV-7 persists in a latent state in the majority of cases; (iii) the presence of EBV seems to be associated with the diseased state of the patient and site.

Ancillary