Cargando…

Characterization of the immune response in ganglia after primary simian varicella virus infection

Primary simian varicella virus (SVV) infection in non-human primates causes varicella, after which the virus becomes latent in ganglionic neurons and reactivates to cause zoster. The host response in ganglia during establishment of latency is ill-defined. Ganglia from five African green monkeys (AGM...

Descripción completa

Detalles Bibliográficos
Autores principales: Ouwendijk, Werner J. D., Getu, Sarah, Mahalingam, Ravi, Gilden, Don, Osterhaus, Albert D. M. E., Verjans, Georges M. G. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899505/
https://www.ncbi.nlm.nih.gov/pubmed/26676825
http://dx.doi.org/10.1007/s13365-015-0408-1
_version_ 1782436473047351296
author Ouwendijk, Werner J. D.
Getu, Sarah
Mahalingam, Ravi
Gilden, Don
Osterhaus, Albert D. M. E.
Verjans, Georges M. G. M.
author_facet Ouwendijk, Werner J. D.
Getu, Sarah
Mahalingam, Ravi
Gilden, Don
Osterhaus, Albert D. M. E.
Verjans, Georges M. G. M.
author_sort Ouwendijk, Werner J. D.
collection PubMed
description Primary simian varicella virus (SVV) infection in non-human primates causes varicella, after which the virus becomes latent in ganglionic neurons and reactivates to cause zoster. The host response in ganglia during establishment of latency is ill-defined. Ganglia from five African green monkeys (AGMs) obtained at 9, 13, and 20 days post-intratracheal SVV inoculation (dpi) were analyzed by ex vivo flow cytometry, immunohistochemistry, and in situ hybridization. Ganglia at 13 and 20 dpi exhibited mild inflammation. Immune infiltrates consisted mostly of CD8(dim) and CD8(bright) memory T cells, some of which expressed granzyme B, and fewer CD11c(+) and CD68(+) cells. Chemoattractant CXCL10 transcripts were expressed in neurons and infiltrating inflammatory cells but did not co-localize with SVV open reading frame 63 (ORF63) RNA expression. Satellite glial cells expressed increased levels of activation markers CD68 and MHC class II at 13 and 20 dpi compared to those at 9 dpi. Overall, local immune responses emerged as viral DNA load in ganglia declined, suggesting that intra-ganglionic immunity contributes to restricting SVV replication.
format Online
Article
Text
id pubmed-4899505
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-48995052016-06-27 Characterization of the immune response in ganglia after primary simian varicella virus infection Ouwendijk, Werner J. D. Getu, Sarah Mahalingam, Ravi Gilden, Don Osterhaus, Albert D. M. E. Verjans, Georges M. G. M. J Neurovirol Article Primary simian varicella virus (SVV) infection in non-human primates causes varicella, after which the virus becomes latent in ganglionic neurons and reactivates to cause zoster. The host response in ganglia during establishment of latency is ill-defined. Ganglia from five African green monkeys (AGMs) obtained at 9, 13, and 20 days post-intratracheal SVV inoculation (dpi) were analyzed by ex vivo flow cytometry, immunohistochemistry, and in situ hybridization. Ganglia at 13 and 20 dpi exhibited mild inflammation. Immune infiltrates consisted mostly of CD8(dim) and CD8(bright) memory T cells, some of which expressed granzyme B, and fewer CD11c(+) and CD68(+) cells. Chemoattractant CXCL10 transcripts were expressed in neurons and infiltrating inflammatory cells but did not co-localize with SVV open reading frame 63 (ORF63) RNA expression. Satellite glial cells expressed increased levels of activation markers CD68 and MHC class II at 13 and 20 dpi compared to those at 9 dpi. Overall, local immune responses emerged as viral DNA load in ganglia declined, suggesting that intra-ganglionic immunity contributes to restricting SVV replication. Springer US 2015-12-16 2016 /pmc/articles/PMC4899505/ /pubmed/26676825 http://dx.doi.org/10.1007/s13365-015-0408-1 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Ouwendijk, Werner J. D.
Getu, Sarah
Mahalingam, Ravi
Gilden, Don
Osterhaus, Albert D. M. E.
Verjans, Georges M. G. M.
Characterization of the immune response in ganglia after primary simian varicella virus infection
title Characterization of the immune response in ganglia after primary simian varicella virus infection
title_full Characterization of the immune response in ganglia after primary simian varicella virus infection
title_fullStr Characterization of the immune response in ganglia after primary simian varicella virus infection
title_full_unstemmed Characterization of the immune response in ganglia after primary simian varicella virus infection
title_short Characterization of the immune response in ganglia after primary simian varicella virus infection
title_sort characterization of the immune response in ganglia after primary simian varicella virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899505/
https://www.ncbi.nlm.nih.gov/pubmed/26676825
http://dx.doi.org/10.1007/s13365-015-0408-1
work_keys_str_mv AT ouwendijkwernerjd characterizationoftheimmuneresponseingangliaafterprimarysimianvaricellavirusinfection
AT getusarah characterizationoftheimmuneresponseingangliaafterprimarysimianvaricellavirusinfection
AT mahalingamravi characterizationoftheimmuneresponseingangliaafterprimarysimianvaricellavirusinfection
AT gildendon characterizationoftheimmuneresponseingangliaafterprimarysimianvaricellavirusinfection
AT osterhausalbertdme characterizationoftheimmuneresponseingangliaafterprimarysimianvaricellavirusinfection
AT verjansgeorgesmgm characterizationoftheimmuneresponseingangliaafterprimarysimianvaricellavirusinfection