J Gen Virol Try Microbiology Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 70 (1989), 2007-2015; DOI 10.1099/0022-1317-70-8-2007
© 1989 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Viljoen, G. J.
Right arrow Articles by Huismans, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Viljoen, G. J.
Right arrow Articles by Huismans, H.
Agricola
Right arrow Articles by Viljoen, G. J.
Right arrow Articles by Huismans, H.

The Characterization of Equine Encephalosis Virus and the Development of Genomic Probes

G. J. Viljoen1 and H. Huismans2

1 Department of Biochemistry, Veterinary Research Institute, Onderstepoort 0110
and2 Department of Genetics, University of Pretoria, Pretoria 0002, South Africa

Equine encephalosis virus (EEV) is an orbivirus associated with a peracute illness of horses in southern Africa. The virus has now been partially purified for the first time and characterized on a molecular level. The virion is composed of 10 dsRNA segments and a protein capsid consisting of at least seven structural proteins that vary in Mr from 36 000 to 120 000. Partial clones of six of the dsRNA segments of EEV serotype Cascara were obtained and analysed for possible use as serotype-specific or group-specific probes in the detection of EEV dsRNA. Cloned fragments of genome segments 3, 8 and 10 were found to show high conservation of these segments, hybridizing to dsRNA from the six EEV serotypes under conditions that indicated more than 90% sequence homology. The genome segment 2-specific probe did not hybridize with dsRNA from any of the other EEV serotypes, suggesting that this segment encodes the serotype-specific antigen of EEV. Cross-hybridization of probes from genome segments 3 and 5 with dsRNA from bluetongue virus (BTV), epizootic haemorrhagic disease virus (EHDV) and African horse sickness virus (AHSV) indicated that EEV is more closely related to BTV and EHDV than to AHSV. Both probes can be used to distinguish between EEV and AHSV dsRNA.

Keywords: EEV, genomic probes, orbiviruses

Received 28 November 1988; accepted 22 March 1989.


This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
A. C. Potgieter, A. D. Steele, and A. A. van Dijk
Cloning of complete genome sets of six dsRNA viruses using an improved cloning method for large dsRNA genes
J. Gen. Virol., September 1, 2002; 83(9): 2215 - 2223.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1989 by the Society for General Microbiology.