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Comparison of the Neuropathology Induced by Two West Nile Virus Strains
Some strains of West Nile virus (WNV) are neuroinvasive and may induce fatal encephalitis/meningitis in a variety of animal species including humans. Whether, however, there is a strain-specific signature in the brain is as yet unknown. Here we investigated the neuropathogenesis induced by two phylo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867487/ https://www.ncbi.nlm.nih.gov/pubmed/24367664 http://dx.doi.org/10.1371/journal.pone.0084473 |
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author | Donadieu, Emilie Lowenski, Steeve Servely, Jean-Luc Laloy, Eve Lilin, Thomas Nowotny, Norbert Richardson, Jennifer Zientara, Stéphan Lecollinet, Sylvie Coulpier, Muriel |
author_facet | Donadieu, Emilie Lowenski, Steeve Servely, Jean-Luc Laloy, Eve Lilin, Thomas Nowotny, Norbert Richardson, Jennifer Zientara, Stéphan Lecollinet, Sylvie Coulpier, Muriel |
author_sort | Donadieu, Emilie |
collection | PubMed |
description | Some strains of West Nile virus (WNV) are neuroinvasive and may induce fatal encephalitis/meningitis in a variety of animal species including humans. Whether, however, there is a strain-specific signature in the brain is as yet unknown. Here we investigated the neuropathogenesis induced by two phylogenetically distant WNV strains of lineage 1, WNV(IS98) and WNV(KUN35 911). While four-week old C57Bl/6J mice were susceptible to both strains and succumbed rapidly after intraperitoneal inoculation, differences were observed in virulence and clinical disease. WNV(KUN35 911), the less virulent strain as judged by determination of LD(50), induced typical signs of encephalitis. Such signs were not observed in WNV(IS98)-infected mice, although they died more rapidly. Histological examination of brain sections also revealed differences, as the level of apoptosis and inflammation was higher in WNV(KUN35 911)- than WNV(IS98)-infected mice. Moreover, staining for cleaved caspase 3 showed that the two WNV strains induced apoptotic death through different molecular mechanisms in one particular brain area. Finally, the two strains showed similar tropism in cortex, striatum, brainstem, and cerebellum but a different one in hippocampus. In summary, our data show that, upon peripheral administration, WNV(IS98) and WNV(KUN35 911) strains induce partially distinct lesions and tissue tropism in the brain. They suggest that the virulence of a WNV strain is not necessarily correlated with the severity of apoptotic and inflammatory lesions in the brain. |
format | Online Article Text |
id | pubmed-3867487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38674872013-12-23 Comparison of the Neuropathology Induced by Two West Nile Virus Strains Donadieu, Emilie Lowenski, Steeve Servely, Jean-Luc Laloy, Eve Lilin, Thomas Nowotny, Norbert Richardson, Jennifer Zientara, Stéphan Lecollinet, Sylvie Coulpier, Muriel PLoS One Research Article Some strains of West Nile virus (WNV) are neuroinvasive and may induce fatal encephalitis/meningitis in a variety of animal species including humans. Whether, however, there is a strain-specific signature in the brain is as yet unknown. Here we investigated the neuropathogenesis induced by two phylogenetically distant WNV strains of lineage 1, WNV(IS98) and WNV(KUN35 911). While four-week old C57Bl/6J mice were susceptible to both strains and succumbed rapidly after intraperitoneal inoculation, differences were observed in virulence and clinical disease. WNV(KUN35 911), the less virulent strain as judged by determination of LD(50), induced typical signs of encephalitis. Such signs were not observed in WNV(IS98)-infected mice, although they died more rapidly. Histological examination of brain sections also revealed differences, as the level of apoptosis and inflammation was higher in WNV(KUN35 911)- than WNV(IS98)-infected mice. Moreover, staining for cleaved caspase 3 showed that the two WNV strains induced apoptotic death through different molecular mechanisms in one particular brain area. Finally, the two strains showed similar tropism in cortex, striatum, brainstem, and cerebellum but a different one in hippocampus. In summary, our data show that, upon peripheral administration, WNV(IS98) and WNV(KUN35 911) strains induce partially distinct lesions and tissue tropism in the brain. They suggest that the virulence of a WNV strain is not necessarily correlated with the severity of apoptotic and inflammatory lesions in the brain. Public Library of Science 2013-12-18 /pmc/articles/PMC3867487/ /pubmed/24367664 http://dx.doi.org/10.1371/journal.pone.0084473 Text en © 2013 Donadieu et al 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 Donadieu, Emilie Lowenski, Steeve Servely, Jean-Luc Laloy, Eve Lilin, Thomas Nowotny, Norbert Richardson, Jennifer Zientara, Stéphan Lecollinet, Sylvie Coulpier, Muriel Comparison of the Neuropathology Induced by Two West Nile Virus Strains |
title | Comparison of the Neuropathology Induced by Two West Nile Virus Strains |
title_full | Comparison of the Neuropathology Induced by Two West Nile Virus Strains |
title_fullStr | Comparison of the Neuropathology Induced by Two West Nile Virus Strains |
title_full_unstemmed | Comparison of the Neuropathology Induced by Two West Nile Virus Strains |
title_short | Comparison of the Neuropathology Induced by Two West Nile Virus Strains |
title_sort | comparison of the neuropathology induced by two west nile virus strains |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867487/ https://www.ncbi.nlm.nih.gov/pubmed/24367664 http://dx.doi.org/10.1371/journal.pone.0084473 |
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