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Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection
Canine distemper virus (CDV), belonging to the genus Morbillivirus, is a highly contagious pathogen. It is infectious in a wide range of host species, including domestic and wildlife carnivores, and causes severe systemic disease with involvement of the respiratory tract. In the present study, canin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144441/ https://www.ncbi.nlm.nih.gov/pubmed/37112814 http://dx.doi.org/10.3390/v15040834 |
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author | Chludzinski, Elisa Ciurkiewicz, Małgorzata Stoff, Melanie Klemens, Johanna Krüger, Johannes Shin, Dai-Lun Herrler, Georg Beineke, Andreas |
author_facet | Chludzinski, Elisa Ciurkiewicz, Małgorzata Stoff, Melanie Klemens, Johanna Krüger, Johannes Shin, Dai-Lun Herrler, Georg Beineke, Andreas |
author_sort | Chludzinski, Elisa |
collection | PubMed |
description | Canine distemper virus (CDV), belonging to the genus Morbillivirus, is a highly contagious pathogen. It is infectious in a wide range of host species, including domestic and wildlife carnivores, and causes severe systemic disease with involvement of the respiratory tract. In the present study, canine precision-cut lung slices (PCLSs) were infected with CDV (strain R252) to investigate temporospatial viral loads, cell tropism, ciliary activity, and local immune responses during early infection ex vivo. Progressive viral replication was observed during the infection period in histiocytic and, to a lesser extent, epithelial cells. CDV-infected cells were predominantly located within the bronchial subepithelial tissue. Ciliary activity was reduced in CDV-infected PCLSs, while viability remained unchanged when compared to controls. MHC-II expression was increased in the bronchial epithelium on day three postinfection. Elevated levels of anti-inflammatory cytokines (interleukin-10 and transforming growth factor-β) were observed in CDV-infected PCLSs on day one postinfection. In conclusion, the present study demonstrates that PCLSs are permissive for CDV. The model reveals an impaired ciliary function and an anti-inflammatory cytokine response, potentially fostering viral replication in the lung during the early phase of canine distemper. |
format | Online Article Text |
id | pubmed-10144441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101444412023-04-29 Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection Chludzinski, Elisa Ciurkiewicz, Małgorzata Stoff, Melanie Klemens, Johanna Krüger, Johannes Shin, Dai-Lun Herrler, Georg Beineke, Andreas Viruses Article Canine distemper virus (CDV), belonging to the genus Morbillivirus, is a highly contagious pathogen. It is infectious in a wide range of host species, including domestic and wildlife carnivores, and causes severe systemic disease with involvement of the respiratory tract. In the present study, canine precision-cut lung slices (PCLSs) were infected with CDV (strain R252) to investigate temporospatial viral loads, cell tropism, ciliary activity, and local immune responses during early infection ex vivo. Progressive viral replication was observed during the infection period in histiocytic and, to a lesser extent, epithelial cells. CDV-infected cells were predominantly located within the bronchial subepithelial tissue. Ciliary activity was reduced in CDV-infected PCLSs, while viability remained unchanged when compared to controls. MHC-II expression was increased in the bronchial epithelium on day three postinfection. Elevated levels of anti-inflammatory cytokines (interleukin-10 and transforming growth factor-β) were observed in CDV-infected PCLSs on day one postinfection. In conclusion, the present study demonstrates that PCLSs are permissive for CDV. The model reveals an impaired ciliary function and an anti-inflammatory cytokine response, potentially fostering viral replication in the lung during the early phase of canine distemper. MDPI 2023-03-24 /pmc/articles/PMC10144441/ /pubmed/37112814 http://dx.doi.org/10.3390/v15040834 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chludzinski, Elisa Ciurkiewicz, Małgorzata Stoff, Melanie Klemens, Johanna Krüger, Johannes Shin, Dai-Lun Herrler, Georg Beineke, Andreas Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection |
title | Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection |
title_full | Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection |
title_fullStr | Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection |
title_full_unstemmed | Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection |
title_short | Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection |
title_sort | canine distemper virus alters defense responses in an ex vivo model of pulmonary infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144441/ https://www.ncbi.nlm.nih.gov/pubmed/37112814 http://dx.doi.org/10.3390/v15040834 |
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