Abstract
Ten aborted foals, diagnosed as infected with Equine Herpes Virus 1 (EHV-1) on histopathological criteria, were examined for the presence of EHV-1 using immunohistology as the investigative instrument. The primary reagent was an antiserum specific for viral envelope glycoproteins. Immunohistology localised EHV-1 to areas of liver necrosis and to the cytoplasm of infected Kupffer cells and hepatocytes. Cytoplasmic immunolabelling was also prominent in reticular cells of the red pulp of the spleen and in intact and degenerated bronchiolar epithelium. Cytoplasmic immunolabelling was seen in morphologically unchanged cells and in cells containing intranuclear inclusion bodies. Three aborted foetuses with no histological signs of EHV-1 infection were negative when immunostained for EHV-1.
Detection by electron microscopy of EHV-1 virions confirmed the EHV-1 specificity of the immunolabelling procedure.
Keywords: equine virus abortion, immunolabelling, tissue sections
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Acknowledgments
The authors wish to thank Miss Cajsa Magnusson, Mrs. Lena Ekman and Mr. Bengt Ekberg for technical assistance and Mrs. Ulla Malmström for preparing the manuscript. Prof. Claes Rehbinder and Ass. Prof. Berndt Klingebom are gratefully acknowledged for critically evaluating the results.
References
- Allen G, Bryans J. Molecular epizootology, pathogenesis and prophylaxis of equine herpesvirus-1 infections. Prog. Vet. Microbiol. Immun. 1986;2:78–144. [PubMed] [Google Scholar]
- Arhelger R, Darlington R, Randall C. An electron microscopic study of equine abortion virus infection in hamster liver. Amer. J. Pathol. 1963;42:703–707. [PMC free article] [PubMed] [Google Scholar]
- Bradford M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry. 1976;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Bürki F, Bäriswyl K, Lindt S. Nachweis des Virus der Equiner Rhinopneumonitis als Ursache von Stutenaborten. (Demonstration of equine rhino pneumonitis virus as a cause of abortion in mares) Schw. Arch. Tierheilk. 1965;107:386–392. [Google Scholar]
- Campbell T, Studdert M. Equine herpesvirus type 1. Vet. Bull. 1983;53:135–146. [Google Scholar]
- Chowdhury S, Kubin G, Ludwig H. Equine herpesvirus type 1 (EHV-1) induced abortions and paralysis in a lipizzaner stud: a contribution to the classification of equine herpesviruses. Arch. Virol. 1986;90:273–288. doi: 10.1007/BF01317376. [DOI] [PubMed] [Google Scholar]
- Darlington R, Moss L. Herpesvirus envelopment. J. Virol. 1968;2:48–55. doi: 10.1128/JVI.2.1.48-55.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Darlington R, Moss L. The envelope of herpesvirus. Progr. Med. Virol. 1969;11:16–45. [PubMed] [Google Scholar]
- Fong C, Hsiung G. Development of an equine herpesvirus in two cell culture systems: light and electron microscopy. Infect. Immunity. 1972;6:865–876. doi: 10.1128/IAI.6.5.865-876.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gimeno E, Nosetto E, Martin A, Galosi C, Ando Y, Etcheverrigaray M. Demonstration of equine herpes virus 1 (EHV-1) in histological sections and tissue cultures by the peroxidaseantiperoxidase technique. J. Vet. Med. 1987;34:740–742. doi: 10.1111/j.1439-0450.1987.tb00455.x. [DOI] [PubMed] [Google Scholar]
- Howard CR, Sundquist B, Allan J, Brown SE, Chen S-H, Morein B. Preparation and properties of immune-stimulating complexes containing hepatitis B virus surface antigen. J. gen. Virol. 1987;68:2281–2289. doi: 10.1099/0022-1317-68-9-2281. [DOI] [PubMed] [Google Scholar]
- Jeleff W. Beitrag zur fetalen Histopathologie des Virusabortes der Stute mit besonderer Berücksichtigung der Differential Diagnose. (Contribution to the fetal histopathology of equine virus abortion, with special attention to the differential diagnosis) Arch. Exp. Vet. Med. 1957;11:906–920. [Google Scholar]
- Kyhse-Andersen J. Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose. J. Biochem. Biophys. Methods. 1984;10:203–209. doi: 10.1016/0165-022X(84)90040-X. [DOI] [PubMed] [Google Scholar]
- Laemmli U K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227:680. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Morein B, Sundquist B, Höglund S, Dalsgaard K, Osterhaus A. ISCOM. A novel structure for antigenic presentation of membrane proteins from enveloped viruses. Nature. 1984;308:457–460. doi: 10.1038/308457a0. [DOI] [PubMed] [Google Scholar]
- Nii S, Morgan C, Rose H. Electron microscopy of herpes simplex virus. J. Virol. 1968;2:517–536. doi: 10.1128/JVI.2.5.517-536.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O’Neill F, Issel C, Henk W. Electron microscopy of equine respiratory viruses in organ cultures of equine fetal respiratory tract epithelium. Amer. J. Vet. Res. 1984;45:1953–1960. [PubMed] [Google Scholar]
- Prickett M: The pathology of disease caused by equine herpesvirus 1. Proc. 2nd Int. Conf. Equine Infectious Diseases 1970, p. 24–33.
- Turtinen I: Studies on the antigenic and genetic variation between the two subtypes of equine herpesvirus-1. PhD. diss., University of Kentucky, 1983.
- Westerfield C, Dimock W. The pathology of equine virus abortion. J. Amer. vet. med. Ass. 1946;109:101–111. [PubMed] [Google Scholar]
- Wong F, Spearman J, Smolenski M, Loewen P. Equine parvovirus: initial isolation and partial characterization. Can. J. comp. Med. 1985;49:50–54. [PMC free article] [PubMed] [Google Scholar]
