黑料网

Human Herpes Viruses in Patients with Chronic Periodontitis and Aggressive Periodontitis

Microbiology Unit, Department of Clinical Pathology, Ain Shams University Hospitals, Cairo, Egypt

*Corresponding Author:

Mona Z Zaghloul
Microbiology Unit, Department of Clinical Pathology
Ain Shams University Hospitals, Cairo, Egypt
Tel: 02-24023494
E-mail: monazaki_810@hotmail.com

Received Date: June 16, 2014; Accepted Date: June 17, 2014; Published Date: June 23, 2014

Citation: Zaghloul MZ (2014) Human Herpes Viruses in Patients with Chronic Periodontitis and Aggressive Periodontitis. Air Water Borne Diseases 3:e131. doi:10.4172/2167-7719.1000e131

Copyright: © 2014 Zaghloul MZ. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Air & Water Borne Diseases

Editorial

The pathogenesis of periodontal disease is a multifactorial process characterized by a complex interaction between the microbial and host factors and a variety of disease- modulatory environmental factors [1]. Recent microbiological researches on periodontal disease are focused on the possible involvement of human viruses in the etiology and pathogenesis of destructive periodontal diseases [2-5]. Herpes viruses are frequently found in periodontal pockets and may initiate or accelerate periodontal tissue destruction because of a virally mediated release of cytokines or even an impairment of the periodontal tissue defense mechanism, resulting in a heightened virulence of resident pathogenic bacteria [6-8]. Human herpes viruses are classified into eight distinct species: Herpes simplex virus (HSV) 1 and 2, Varicella zoster virus (VZV), Human Cytomegalovirus (HCMV), Epstein - Barr Virus (EBV) and human Herpes virus 6, human Herpes virus 7, and human Herpes virus 8 or Karposi's sarcoma-associated herpes virus [9]. Human cytomegalovirus (HCMV) and Epstien barr virus 1 (EBV-1) are involved in the pathogenesis of human periodontal disease. These viruses are capable of infecting and impairing Poly Morpho Nuclear Leukocytes (PMNs), macrophages and lymphocytes. Human cytomegalovirus may contribute to disease progression through the activation of IL1β gene transcription [10]. The reduced host defense by herpes virus-infected cells give rise to overgrowth of pathogenic bacteria that invade the periodontal tissue more efficiently [2].

Chronic periodontitis was defined when at least one of the four sites per tooth with Probing Pocket Depth (PPD) ≥ 3 mm or clinical attachment level (CAL) ≥ 2 mm [11]. While aggressive periodontitis was defined when the four sites per tooth with (PPD) ≥ 6 mm or (CAL) ≥ 5 mm with involvement of incisors and first molar teeth in subjects with age ranging from 18 to 35 years. HSV-1 is most commonly found in the oral cavity as a primary infection and establishes latency within the trigeminal ganglia [12]. Cultured epithelial cells and fibroblasts from clinically healthy human gingiva are susceptible to HSV infection [13] suggesting that those cells could be a reservoir for the latent virus. HSV-1 antigens could be detected in gingival biopsies from periodontally diseased patients using an indirect immunofluorescence assay [14]. Herpes viruses, including HCMV, EBV and HSV-1, can be reactivated from a latent infection either spontaneously or concurrent with another infection or with other stress factors affecting the host immune system [15,16].

References

1. Das S, Krithiga GS, Gopalakrishnan S (2012)
2. Contreras A, Umeda M, Chen C, Bakker I, Morrison JL, et al. (1999)
3. Contreras A, Slots J (1996)
4. Kubar A, Saygun I, Ozdemir A, Yapar M (2005)
5. Saygun I, Sahin S, Ozdemir A, Kurti B, Yapar M, et al. (2002)
6. Saygun I, Kubar A, Ozdemir A, Yapar M, Slots J (2004)
7. Saygun I, Yapar M, Ozdemir A, Kubar A, Slots J (2004)
8. Kamma JJ, Contreras A, Slots J (2001)
9. Chen V, Chen Y, Li H, Kent K, Baumgartner JC, et al. (2009)
10. Wara-Aswapati N, Boch JA, Auron PE (2003)
11. Loe h, Silness j (1963)
12. Zakay-Rones Z, Hochman N, Rones Y (1982)
13. Ehrlich J, Cohen GH, Hochman N (1983)
14. Heling I, Morag-Hezroni M, Marva E, Hochman N, Zakay-Rones Z, et al. (2001)
15. Saboia-Dantas CJ, Coutrin de Toledo LF, Sampaio-Filho HR, Siqueira JF Jr (2007)
16. Slots J, Contreras A (2000)