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Determination of Biofilm Initiation on Virus-infected Cells by Bacteria and Fungi
Published on: July 6, 2016
Herpesviral-bacterial coinfection in periapical pathosis
Mohammad Sabeti1, Jørgen Slots
1School of Dentistry, University of Southern California, Los Angeles 90089-0641, USA.
Abstract:
Two members of the herpesvirus family, human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV), seem to be important putative pathogens of human periodontitis and symptomatic periapical lesions, causing pathosis either by inducing immunosuppression with a subsequent risk of aggressive bacterial infections or by infecting of periodontal cells directly. This study aimed to relate periapical occurrence of HCMV, EBV, and herpes simplex virus active infections to clinical characteristics of periapical lesions and periapical bacterial flora. Microbial samples were collected from 34 periapical lesions in conjunction with periapical surgery. Part of the periapical specimen was frozen for virologic examination, and another part was transferred to anaerobic transport medium for bacteriologic examination. RNA was isolated by means of a guanidinium isothiocyanate-acid phenol procedure, and cDNA was produced using herpesvirus-specific primers and reverse-transcription polymerase chain reaction amplification. Bacteriologic examination was performed according to established anaerobic culture methods. Of the 34 periapical lesions studied, 20 showed both HCMV and EBV, seven showed only HCMV, one showed only EBV, and six showed neither HCMV nor EBV. Herpes simplex virus was detected in two lesions. Higher occurrence of herpesvirus was detected in large versus small periapical lesions (p < 0.001) and in symptomatic versus asymptomatic periapical lesions (p < 0.001). A total of 18 microbial groups and an average of 2.1 to 3.0 bacterial groups were isolated from various categories of periapical lesions. The important finding of this study was that most teeth with necrotic pulp and periapical lesions harbored herpesviruses in periapical granulomatous tissue. Herpesvirus species in cooperation with endodontopathic bacteria may play major roles in the etiopathogenesis of aggressive types of periapical pathosis in humans.
Insights
Herpesviruses like human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV) are frequently found in periapical lesions. Their presence correlates with larger, symptomatic lesions, suggesting a role in aggressive periapical disease alongside bacteria.
Area of Science:
- Oral Microbiology
- Virology
- Infectious Diseases
Background:
- Herpesviruses, including human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV), are implicated as potential pathogens in human periodontitis and periapical lesions.
- These viruses may contribute to disease by causing immunosuppression, increasing susceptibility to bacterial infections, or directly infecting periodontal cells.
Purpose of the Study:
- To investigate the association between active infections of HCMV, EBV, and herpes simplex virus (HSV) in periapical lesions.
- To correlate the presence of these viruses with clinical characteristics of periapical lesions and the associated bacterial flora.
Main Methods:
- Microbial samples were collected from 34 periapical lesions during surgery.
- Virologic examination involved RNA isolation, cDNA production, and reverse-transcription polymerase chain reaction (RT-PCR) for herpesviruses.
- Bacteriologic examination utilized established anaerobic culture methods.
Main Results:
- HCMV and EBV were detected in 20 of 34 lesions; HCMV alone in seven, EBV alone in one, and neither in six.
- HSV was detected in two lesions.
- Herpesvirus occurrence was significantly higher in large (p < 0.001) and symptomatic (p < 0.001) periapical lesions.
- An average of 2.1 to 3.0 bacterial groups were isolated per lesion.
Conclusions:
- Most teeth with necrotic pulp and periapical lesions harbor herpesviruses within the periapical granulomatous tissue.
- Herpesviruses, in conjunction with endodontopathic bacteria, likely play a significant role in the pathogenesis of aggressive periapical diseases.
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