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Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.

Dorsal root ganglion neurons, which express herpes simplex virus (HSV) latency-associated transcript (LAT) during experimental latent infection, were investigated by in situ hybridization. The number of LAT-positive neurons was determined by examination of ganglion serial sections. In other latently...

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Detalles Bibliográficos
Autores principales: Tenser, R. B., Edris, W. A., Hay, K. A.
Formato: Texto
Lenguaje:English
Publicado: Yale Journal of Biology and Medicine 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589233/
https://www.ncbi.nlm.nih.gov/pubmed/2773515
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author Tenser, R. B.
Edris, W. A.
Hay, K. A.
author_facet Tenser, R. B.
Edris, W. A.
Hay, K. A.
author_sort Tenser, R. B.
collection PubMed
description Dorsal root ganglion neurons, which express herpes simplex virus (HSV) latency-associated transcript (LAT) during experimental latent infection, were investigated by in situ hybridization. The number of LAT-positive neurons was determined by examination of ganglion serial sections. In other latently infected mice, the number of ganglion neurons that reactivated HSV antigen after explant culture was determined in serial sections. LAT was detected in 100 percent of ganglia, with an average of 19.5 LAT-positive neurons per ganglion. After explant culture of latently infected ganglia (in the presence of colchicine to decrease spread of reactivated virus), HSV antigen was detected in 94 percent of ganglia, with an average of 13.1 positive neurons in the antigen-positive ganglia. The similar quantities of LAT- and antigen-positive neurons within ganglia support the hypothesis that LAT-positive neurons were the neurons from which HSV was reactivated.
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spelling pubmed-25892332008-11-28 Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons. Tenser, R. B. Edris, W. A. Hay, K. A. Yale J Biol Med Research Article Dorsal root ganglion neurons, which express herpes simplex virus (HSV) latency-associated transcript (LAT) during experimental latent infection, were investigated by in situ hybridization. The number of LAT-positive neurons was determined by examination of ganglion serial sections. In other latently infected mice, the number of ganglion neurons that reactivated HSV antigen after explant culture was determined in serial sections. LAT was detected in 100 percent of ganglia, with an average of 19.5 LAT-positive neurons per ganglion. After explant culture of latently infected ganglia (in the presence of colchicine to decrease spread of reactivated virus), HSV antigen was detected in 94 percent of ganglia, with an average of 13.1 positive neurons in the antigen-positive ganglia. The similar quantities of LAT- and antigen-positive neurons within ganglia support the hypothesis that LAT-positive neurons were the neurons from which HSV was reactivated. Yale Journal of Biology and Medicine 1989 /pmc/articles/PMC2589233/ /pubmed/2773515 Text en
spellingShingle Research Article
Tenser, R. B.
Edris, W. A.
Hay, K. A.
Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
title Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
title_full Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
title_fullStr Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
title_full_unstemmed Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
title_short Herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
title_sort herpes simplex latent infection: quantitation of latency-associated transcript-positive neurons and reactivable neurons.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589233/
https://www.ncbi.nlm.nih.gov/pubmed/2773515
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