Identification of Epstein-Barr Virus in the Human Placenta and Its Pathologic Characteristics.
10.3346/jkms.2017.32.12.1959
- Author:
Younghoon KIM
1
;
Hye Sung KIM
;
Joong Shin PARK
;
Chong Jai KIM
;
Woo Ho KIM
Author Information
1. Department of Pathology, Seoul National University College of Medicine, Seoul, Korea. woohokim@snu.ac.kr
- Publication Type:Original Article
- Keywords:
Human Herpesvirus 4;
Image Cytometry;
In Situ Hybridization;
Virus Latency;
Decidua Capsularis
- MeSH:
Decidua;
Depression;
Epithelial Cells;
Epstein-Barr Virus Infections;
Female;
Gene Expression;
Herpesvirus 4, Human*;
Humans*;
Image Cytometry;
In Situ Hybridization;
Mass Screening;
Membranes;
Pathology;
Placenta*;
Pre-Eclampsia;
Pregnant Women;
RNA, Messenger;
Silver;
Stillbirth;
Virus Latency
- From:Journal of Korean Medical Science
2017;32(12):1959-1966
- CountryRepublic of Korea
- Language:English
-
Abstract:
Epstein-Barr virus (EBV), a common pathogen in humans, is suspected as the cause of multiple pregnancy-related pathologies including depression, preeclampsia, and stillbirth. Moreover, transmission of EBV through the placenta has been reported. However, the focus of EBV infection within the placenta has remained unknown to date. In this study, we proved the expression of latent EBV genes in the endometrial glandular epithelial cells of the placenta and investigated the cytological characteristics of these cells. Sixty-eight placentas were obtained from pregnant women. Tissue microarray was constructed. EBV latent genes including EBV-encoding RNA-1 (EBER1), Epstein-Barr virus nuclear antigen 1 (EBNA1), late membrane antigen (LMP1), and RPMS1 were detected with silver in situ hybridization and/or mRNA in situ hybridization. Nuclear features of EBV-positive cells in EBV-infected placenta were compared with those of EBV-negative cells via image analysis. Sixteen placentas (23.5%) showed positive expression of all 4 EBV latent genes; only the glandular epithelial cells of the decidua showed EBV gene expression. EBV infection status was not significantly correlated with maternal, fetal, or placental factors. The nuclei of EBV-positive cells were significantly larger, longer, and round-shaped than those of EBV-negative cells regardless of EBV-infection status of the placenta. For the first time, evidence of EBV gene expression has been shown in placental tissues. Furthermore, we have characterized its cytological features, allowing screening of EBV infection through microscopic examination.
