Detection of latency-associated transcripts of equid herpesvirus 1 in equine leukocytes but not in trigeminal ganglia

Author:

Chesters P M1,Allsop R1,Purewal A1,Edington N1

Affiliation:

1. Department of Pathology and Infectious Diseases, The Royal Veterinary College, London, United Kingdom.

Abstract

Results from Southern hybridization and PCR amplification experiments using a randomly synthesized reverse transcription-PCR product showed that peripheral blood leukocytes from horses showing no clinical signs of disease expressed a putative latency-associated transcript antisense to and overlapping the 3' end of the equid herpesvirus 1 (EHV-1) immediate-early gene (gene 64). A PCR product derived from this transcript has > or =96% identity with the published EHV-1 sequence. In situ hybridization studies of equine bronchial lymph nodes corroborated these findings and are consistent with reactivation data (D. A. Smith, A. Hamblin, and N. Edington, unpublished data), indicating that EHV-1 latency is established predominantly in CD5+/CD8+ leukocytes.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference36 articles.

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3. The detection of latency-associated transcripts of equine herpesvirus 1 in ganglionic neurons;Baxi M. K.;J. Gen. Virol.,1995

4. Latency of equine herpes virus 4 (equine rhinopneumonitis);Browning G. F.;Vet. Rec.,1988

5. Gene sequence and mapping data from Marek's disease virus and herpesvirus of turkeys: implications for herpesvirus classification;Buckmaster A. E.;J. Gen. Virol.,1988

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