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Lytic Promoters Express Protein during Herpes Simplex Virus Latency
Herpes simplex virus (HSV) has provided the prototype for viral latency with previously well-defined acute or lytic and latent phases. More recently, the deep quiescence of HSV latency has been questioned with evidence that lytic genes can be transcribed in this state. However, to date the only evid...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922595/ https://www.ncbi.nlm.nih.gov/pubmed/27348812 http://dx.doi.org/10.1371/journal.ppat.1005729 |
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author | Russell, Tiffany A. Tscharke, David C. |
author_facet | Russell, Tiffany A. Tscharke, David C. |
author_sort | Russell, Tiffany A. |
collection | PubMed |
description | Herpes simplex virus (HSV) has provided the prototype for viral latency with previously well-defined acute or lytic and latent phases. More recently, the deep quiescence of HSV latency has been questioned with evidence that lytic genes can be transcribed in this state. However, to date the only evidence that these transcripts might be translated has come from immunological studies that show activated T cells persist in the nervous system during latency. Here we use a highly sensitive Cre-marking model to show that lytic and latent phases are less clearly defined in two significant ways. First, around half of the HSV spread leading to latently infected sites occurred beyond the initial acute infection and second, we show direct evidence that lytic promoters can drive protein expression during latency. |
format | Online Article Text |
id | pubmed-4922595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49225952016-07-18 Lytic Promoters Express Protein during Herpes Simplex Virus Latency Russell, Tiffany A. Tscharke, David C. PLoS Pathog Research Article Herpes simplex virus (HSV) has provided the prototype for viral latency with previously well-defined acute or lytic and latent phases. More recently, the deep quiescence of HSV latency has been questioned with evidence that lytic genes can be transcribed in this state. However, to date the only evidence that these transcripts might be translated has come from immunological studies that show activated T cells persist in the nervous system during latency. Here we use a highly sensitive Cre-marking model to show that lytic and latent phases are less clearly defined in two significant ways. First, around half of the HSV spread leading to latently infected sites occurred beyond the initial acute infection and second, we show direct evidence that lytic promoters can drive protein expression during latency. Public Library of Science 2016-06-27 /pmc/articles/PMC4922595/ /pubmed/27348812 http://dx.doi.org/10.1371/journal.ppat.1005729 Text en © 2016 Russell, Tscharke http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Russell, Tiffany A. Tscharke, David C. Lytic Promoters Express Protein during Herpes Simplex Virus Latency |
title | Lytic Promoters Express Protein during Herpes Simplex Virus Latency |
title_full | Lytic Promoters Express Protein during Herpes Simplex Virus Latency |
title_fullStr | Lytic Promoters Express Protein during Herpes Simplex Virus Latency |
title_full_unstemmed | Lytic Promoters Express Protein during Herpes Simplex Virus Latency |
title_short | Lytic Promoters Express Protein during Herpes Simplex Virus Latency |
title_sort | lytic promoters express protein during herpes simplex virus latency |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922595/ https://www.ncbi.nlm.nih.gov/pubmed/27348812 http://dx.doi.org/10.1371/journal.ppat.1005729 |
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