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Human Cytomegalovirus and Epstein-Barr Virus Genotypes in Apical Periodontitis Lesions
Aleksandar Jakovljevic1, Miroslav Andric1, Aleksandra Knezevic2
1School of Dental Medicine, Clinic for Oral Surgery and Implantology, University of Belgrade, Belgrade, Serbia.
Introduction:
Different genotypes of human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV) possess specific pathogenic abilities because of various interactions with the host's immune system and differences in cell tropism. The aim of this study was to determine the distribution of HCMV and EBV genotypes in apical periodontitis lesions in relation to their clinical and histopathologic features.
Methods:
One hundred samples of apical periodontitis lesions and 25 control samples (healthy pulp tissue) were collected. The presence of HCMV glycoprotein B (gB) and EBV nuclear antigen-2 genotypes was analyzed by nested polymerase chain reaction and restriction fragment length polymorphisms analysis.
Results:
EBV and HCMV were detected in apical periodontitis lesions at significantly higher frequencies than in healthy pulp controls (P = .020 and P = .020, respectively). HCMV gB type II was significantly more frequent compared with gB type I in the examined groups (P = .036). No HCMV gB type III or IV products were found. In both periapical lesions and controls, EBV-1 occurred more often compared with EBV-2 (P = .001). Dual EBV and HCMV coinfection was more frequently detected in large-size periapical lesions (P = .038).
Conclusions:
Both HCMV and EBV are associated with inflammatory processes of periapical bone destruction. HCMV gB type II and EBV-1 are the most prevalent genotypes in apical periodontitis lesions.
Insights
Human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV) are linked to apical periodontitis. The study found HCMV gB type II and EBV-1 are the most common genotypes in these lesions.
Area of Science:
- Oral pathology
- Virology
- Immunology
Background:
- Different genotypes of human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV) exhibit distinct pathogenic capabilities.
- These differences arise from variations in host immune system interactions and cellular tropism.
Purpose of the Study:
- To investigate the distribution of HCMV and EBV genotypes in apical periodontitis lesions.
- To correlate viral genotype prevalence with clinical and histopathologic features of the lesions.
Main Methods:
- Nested polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analysis were employed.
- Samples from 100 apical periodontitis lesions and 25 healthy pulp tissues were analyzed.
- HCMV glycoprotein B (gB) and EBV nuclear antigen-2 genotypes were specifically targeted.
Main Results:
- HCMV and EBV were detected more frequently in apical periodontitis lesions than in healthy controls (P = .020 for both).
- HCMV gB type II was significantly more prevalent than type I (P = .036).
- EBV-1 occurred more often than EBV-2 (P = .001), and dual HCMV/EBV coinfection was more common in larger lesions (P = .038).
Conclusions:
- HCMV and EBV are implicated in the inflammatory bone destruction characteristic of apical periodontitis.
- The predominant genotypes found in these lesions are HCMV gB type II and EBV-1.
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