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


     


J Gen Virol 71 (1990), 2593-2598; DOI 10.1099/0022-1317-71-11-2593
© 1990 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 Rodák, L.
Right arrow Articles by Nevoránková, Z.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rodák, L.
Right arrow Articles by Nevoránková, Z.
Agricola
Right arrow Articles by Rodák, L.
Right arrow Articles by Nevoránková, Z.

Monoclonal antibodies to rabbit haemorrhagic disease virus and their use in the diagnosis of infection

L. Rodák, M. Granátová, L. Valícek, B. Smíd, T. Vesely and Z. Nevoránková

Veterinary Research Institute, Hudcova 70, 621 32 Brno, Czechoslovakia

Hybridomas producing monoclonal antibodies (MAbs) to rabbit haemorrhagic disease virus (RHDV) were prepared. Using Western blot (WB) analysis, the MAbs obtained were divided into two groups, one reacting with the major structural proteins of Mr 61K and 38K, and the other giving negative reactions. Both groups of MAbs, however, reacted specifically with RHDV in ELISA and by immunoperoxidase (IP) and immunofluorescence (IF) tests with infected cells. As demonstrated by WB using RHDV-specific MAbs and a MAb to feline calicivirus (FCV) strain F9, the major structural (capsid) proteins of RHDV and FCV have very similar sizes (Mr 61K and 38K compared to 62K to 64K and 40K respectively). No cross-reactions of MAbs with proteins of the other virus were observed in WB analysis, ELISA, IP tests or IF. The high specificity and sensitivity of RHDV-specific MAbs make them suitable for the routine IP and IF diagnosis of RHDV in liver cells of rabbits dying after natural or experimental infections.

Received 21 May 1990; accepted 20 July 1990.


This article has been cited by other articles:


Home page
J. Virol.Home page
T. D. Parker, N. Kitamoto, T. Tanaka, A. M. Hutson, and M. K. Estes
Identification of Genogroup I and Genogroup II Broadly Reactive Epitopes on the Norovirus Capsid
J. Virol., June 15, 2005; 79(12): 7402 - 7409.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
N. L. Forrester, B. Boag, S. R. Moss, S. L. Turner, R. C. Trout, P. J. White, P. J. Hudson, and E. A. Gould
Long-term survival of New Zealand rabbit haemorrhagic disease virus RNA in wild rabbits, revealed by RT-PCR and phylogenetic analysis
J. Gen. Virol., November 1, 2003; 84(11): 3079 - 3086.
[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 © 1990 by the Society for General Microbiology.