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Detection of eastern equine encephalomyelitis virus RNA in formalin-fixed, paraffin-embedded tissues using DNA in situ hybridization.

Abstract
Eastern equine encephalomyelitis (F.EE) virus was detected in infected formalin-fixed horse and emu tissues and in infected chicken embryo fibroblasts. Results of in situ hybridization using a digoxigenin-labeled 40-base DNA probe complementary to a conserved region of the EEE virus RNA compared favorably with results of both virus isolation and serum neutralization tests. This technique may be useful for diagnosis of EEE virus infection in various animal species, especially when fresh tissues are not available for analysis, and also will provide a means for studying the involvement of alphaviruses in pathogenesis studies.
AuthorsC R Gregory, K S Latimer, F D Niagro, R P Campagnoli, W L Steffens, B W Ritchie
JournalJournal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc (J Vet Diagn Invest) Vol. 8 Issue 2 Pg. 151-5 (Apr 1996) ISSN: 1040-6387 [Print] United States
PMID8744734 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA Probes
  • RNA, Ribosomal
  • RNA, Viral
  • RNA, ribosomal, 26S
  • Formaldehyde
  • Paraffin
Topics
  • Animals
  • Base Sequence
  • Birds
  • Cells, Cultured
  • Chick Embryo
  • Conserved Sequence
  • DNA Probes
  • Encephalitis Virus, Eastern Equine (isolation & purification)
  • Encephalomyelitis, Equine (diagnosis, pathology, veterinary)
  • Fibroblasts
  • Formaldehyde
  • Genome, Viral
  • Histological Techniques
  • Horse Diseases
  • Horses
  • In Situ Hybridization (methods)
  • Neutralization Tests (methods)
  • Paraffin
  • RNA, Ribosomal (genetics)
  • RNA, Viral (analysis)

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