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Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus

Human respiratory syncytial virus is an important cause of severe respiratory disease in young children, the elderly, and in immunocompromised adults. Similarly, bovine respiratory syncytial virus (BRSV) is causing severe, sometimes fatal, respiratory disease in calves. Both viruses are pneumovirus...

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Detalles Bibliográficos
Autores principales: Viuff, Birgitte, Tjørnehøj, Kirsten, Larsen, Lars E., Røntved, Christine M., Uttenthal, Åse, Rønsholt, Leif, Alexandersen, Soren
Formato: Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1850917/
https://www.ncbi.nlm.nih.gov/pubmed/12466134
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author Viuff, Birgitte
Tjørnehøj, Kirsten
Larsen, Lars E.
Røntved, Christine M.
Uttenthal, Åse
Rønsholt, Leif
Alexandersen, Soren
author_facet Viuff, Birgitte
Tjørnehøj, Kirsten
Larsen, Lars E.
Røntved, Christine M.
Uttenthal, Åse
Rønsholt, Leif
Alexandersen, Soren
author_sort Viuff, Birgitte
collection PubMed
description Human respiratory syncytial virus is an important cause of severe respiratory disease in young children, the elderly, and in immunocompromised adults. Similarly, bovine respiratory syncytial virus (BRSV) is causing severe, sometimes fatal, respiratory disease in calves. Both viruses are pneumovirus and the infections with human respiratory syncytial virus and BRSV have similar clinical, pathological, and epidemiological characteristics. In this study we used experimental BRSV infection in calves as a model of respiratory syncytial virus infection to demonstrate important aspects of viral replication and clearance in a natural target animal. Replication of BRSV was demonstrated in the luminal part of the respiratory epithelial cells and replication in the upper respiratory tract preceded the replication in the lower respiratory tract. Virus excreted to the lumen of the respiratory tract was cleared by neutrophils whereas apoptosis was an important way of clearance of BRSV-infected epithelial cells. Neighboring cells, which probably were epithelial cells, phagocytized the BRSV-infected apoptotic cells. The number of both CD4(+) and CD8+ T cells increased during the course of infection, but the T cells were not found between the epithelial cells of the bronchi up until apoptosis was no longer detected, thus in the bronchi there was no indication of direct contact-dependent T-cell-mediated cytotoxicity in the primary infection.
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spelling pubmed-18509172007-06-15 Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus Viuff, Birgitte Tjørnehøj, Kirsten Larsen, Lars E. Røntved, Christine M. Uttenthal, Åse Rønsholt, Leif Alexandersen, Soren Am J Pathol Regular Articles Human respiratory syncytial virus is an important cause of severe respiratory disease in young children, the elderly, and in immunocompromised adults. Similarly, bovine respiratory syncytial virus (BRSV) is causing severe, sometimes fatal, respiratory disease in calves. Both viruses are pneumovirus and the infections with human respiratory syncytial virus and BRSV have similar clinical, pathological, and epidemiological characteristics. In this study we used experimental BRSV infection in calves as a model of respiratory syncytial virus infection to demonstrate important aspects of viral replication and clearance in a natural target animal. Replication of BRSV was demonstrated in the luminal part of the respiratory epithelial cells and replication in the upper respiratory tract preceded the replication in the lower respiratory tract. Virus excreted to the lumen of the respiratory tract was cleared by neutrophils whereas apoptosis was an important way of clearance of BRSV-infected epithelial cells. Neighboring cells, which probably were epithelial cells, phagocytized the BRSV-infected apoptotic cells. The number of both CD4(+) and CD8+ T cells increased during the course of infection, but the T cells were not found between the epithelial cells of the bronchi up until apoptosis was no longer detected, thus in the bronchi there was no indication of direct contact-dependent T-cell-mediated cytotoxicity in the primary infection. American Society for Investigative Pathology 2002-12 /pmc/articles/PMC1850917/ /pubmed/12466134 Text en Copyright © 2002, American Society for Investigative Pathology
spellingShingle Regular Articles
Viuff, Birgitte
Tjørnehøj, Kirsten
Larsen, Lars E.
Røntved, Christine M.
Uttenthal, Åse
Rønsholt, Leif
Alexandersen, Soren
Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus
title Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus
title_full Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus
title_fullStr Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus
title_full_unstemmed Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus
title_short Replication and Clearance of Respiratory Syncytial Virus : Apoptosis Is an Important Pathway of Virus Clearance after Experimental Infection with Bovine Respiratory Syncytial Virus
title_sort replication and clearance of respiratory syncytial virus : apoptosis is an important pathway of virus clearance after experimental infection with bovine respiratory syncytial virus
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1850917/
https://www.ncbi.nlm.nih.gov/pubmed/12466134
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