Detection of EHV-1 and EHV-4 in placental sections of naturally occurring EHV-1- and EHV-4-related abortions in the UK: use of the placenta in diagnosis

• Published in: Equine veterinary journal 2003-07, Vol.35 (5), p.430-433
• Main Authors: GERST, S., BORCHERS, K., GOWER, S. M., SMITH, K. C.
• Format: Article
• Language: English
• Subjects: abortion; Abortion, Veterinary - virology; Animals; Antigens, Viral - analysis; diagnosis; DNA, Viral - analysis; Female; Herpesviridae Infections - diagnosis; Herpesviridae Infections - veterinary; herpesvirus; Herpesvirus 1, Equid - genetics; Herpesvirus 1, Equid - immunology; Herpesvirus 1, Equid - isolation & purification; Herpesvirus 4, Equid - genetics; Herpesvirus 4, Equid - immunology; Herpesvirus 4, Equid - isolation & purification; horse; Horse Diseases - diagnosis; Horse Diseases - virology; Horses; Immunohistochemistry - veterinary; In Situ Hybridization - veterinary; placenta; Placenta - pathology; Placenta - virology; Polymerase Chain Reaction - veterinary; Pregnancy
• ISSN: 0425-1644; 2042-3306
• DOI: 10.2746/042516403775600451

Summary Reasons for performing study: EHV‐1 and EHV‐4 abortion diagnosis is based upon detailed examination of the aborted fetus. However, in some cases, only the placenta is available for examination. Furthermore, the contribution of lesions in the placenta to pathogenesis and diagnosis of EHV‐1 and EHV‐4 abortion has been neglected. Objectives: To assess the utility of placental examination in equine herpesvirus‐1 (EHV‐1) and EHV‐4 abortion diagnosis. Methods: Sections of allantochorion from 49 herpesvirus abortions were analysed by PCR, in situ hybridisation and immunostaining. Results: Virus‐specific nested PCR confirmed the presence of viral DNA in 46 cases; 41 cases were EHV‐1‐positive and 5 EHV‐4‐positive. Microscopic changes were nonspecific. Examination of the PCR‐positive sections of allantochorion revealed EHV‐1 DNA by in situ hybridisation (ISH) in 21 cases and EHV‐4 in 4 cases. In 2 samples, DNA of both viruses was present on PCR and ISH. Viral antigen was found by immunohistology in 15 cases. Regarding the localisation of virus in the placentae, both viral DNA and antigen of EHV‐1 and EHV‐4 were found in endothelial cells of chorionic villi and, occasionally, in trophoblast epithelium. In the stromal endothelium, only EHV‐1 was found. Conclusions: The data indicate that examination of placentae is a useful diagnostic aid in EHV‐1 and EHV‐4 abortion diagnosis. Potential relevance: Virological examination of the placenta should be come standard practice in equine abortion investigations, particularly in those cases where the fetus is not available for examination.