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Intracellular Events and Cell Fate in Filovirus Infection
Marburg and Ebola viruses cause a severe hemorrhagic disease in humans with high fatality rates. Early target cells of filoviruses are monocytes, macrophages, and dendritic cells. The infection spreads to the liver, spleen and later other organs by blood and lymph flow. A hallmark of filovirus infec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172725/ https://www.ncbi.nlm.nih.gov/pubmed/21927676 http://dx.doi.org/10.3390/v3081501 |
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author | Olejnik, Judith Ryabchikova, Elena Corley, Ronald B. Mühlberger, Elke |
author_facet | Olejnik, Judith Ryabchikova, Elena Corley, Ronald B. Mühlberger, Elke |
author_sort | Olejnik, Judith |
collection | PubMed |
description | Marburg and Ebola viruses cause a severe hemorrhagic disease in humans with high fatality rates. Early target cells of filoviruses are monocytes, macrophages, and dendritic cells. The infection spreads to the liver, spleen and later other organs by blood and lymph flow. A hallmark of filovirus infection is the depletion of non-infected lymphocytes; however, the molecular mechanisms leading to the observed bystander lymphocyte apoptosis are poorly understood. Also, there is limited knowledge about the fate of infected cells in filovirus disease. In this review we will explore what is known about the intracellular events leading to virus amplification and cell damage in filovirus infection. Furthermore, we will discuss how cellular dysfunction and cell death may correlate with disease pathogenesis. |
format | Online Article Text |
id | pubmed-3172725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-31727252011-09-14 Intracellular Events and Cell Fate in Filovirus Infection Olejnik, Judith Ryabchikova, Elena Corley, Ronald B. Mühlberger, Elke Viruses Review Marburg and Ebola viruses cause a severe hemorrhagic disease in humans with high fatality rates. Early target cells of filoviruses are monocytes, macrophages, and dendritic cells. The infection spreads to the liver, spleen and later other organs by blood and lymph flow. A hallmark of filovirus infection is the depletion of non-infected lymphocytes; however, the molecular mechanisms leading to the observed bystander lymphocyte apoptosis are poorly understood. Also, there is limited knowledge about the fate of infected cells in filovirus disease. In this review we will explore what is known about the intracellular events leading to virus amplification and cell damage in filovirus infection. Furthermore, we will discuss how cellular dysfunction and cell death may correlate with disease pathogenesis. Molecular Diversity Preservation International (MDPI) 2011-08-24 /pmc/articles/PMC3172725/ /pubmed/21927676 http://dx.doi.org/10.3390/v3081501 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Olejnik, Judith Ryabchikova, Elena Corley, Ronald B. Mühlberger, Elke Intracellular Events and Cell Fate in Filovirus Infection |
title | Intracellular Events and Cell Fate in Filovirus Infection |
title_full | Intracellular Events and Cell Fate in Filovirus Infection |
title_fullStr | Intracellular Events and Cell Fate in Filovirus Infection |
title_full_unstemmed | Intracellular Events and Cell Fate in Filovirus Infection |
title_short | Intracellular Events and Cell Fate in Filovirus Infection |
title_sort | intracellular events and cell fate in filovirus infection |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172725/ https://www.ncbi.nlm.nih.gov/pubmed/21927676 http://dx.doi.org/10.3390/v3081501 |
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