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Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species
Measles virus (MV) and canine distemper virus (CDV) are closely related members of the family Paramyxoviridae, genus Morbillivirus. MV infection of humans and non-human primates (NHPs) results in a self-limiting disease, which rarely involves central nervous system (CNS) complications. In contrast,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402773/ https://www.ncbi.nlm.nih.gov/pubmed/34452447 http://dx.doi.org/10.3390/v13081582 |
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author | Laksono, Brigitta M. Tran, Diana N. Kondova, Ivanela van Engelen, Harry G. H. Michels, Samira Nambulli, Sham de Vries, Rory D. Duprex, W. Paul Verjans, Georges M. G. M. de Swart, Rik L. |
author_facet | Laksono, Brigitta M. Tran, Diana N. Kondova, Ivanela van Engelen, Harry G. H. Michels, Samira Nambulli, Sham de Vries, Rory D. Duprex, W. Paul Verjans, Georges M. G. M. de Swart, Rik L. |
author_sort | Laksono, Brigitta M. |
collection | PubMed |
description | Measles virus (MV) and canine distemper virus (CDV) are closely related members of the family Paramyxoviridae, genus Morbillivirus. MV infection of humans and non-human primates (NHPs) results in a self-limiting disease, which rarely involves central nervous system (CNS) complications. In contrast, infection of carnivores with CDV usually results in severe disease, in which CNS complications are common and the case-fatality rate is high. To compare the neurovirulence and neurotropism of MV and CDV, we established a short-term organotypic brain slice culture system of the olfactory bulb, hippocampus, or cortex obtained from NHPs, dogs, and ferrets. Slices were inoculated ex vivo with wild-type-based recombinant CDV or MV expressing a fluorescent reporter protein. The infection level of both morbilliviruses was determined at different times post-infection. We observed equivalent infection levels and identified microglia as main target cells in CDV-inoculated carnivore and MV-inoculated NHP brain tissue slices. Neurons were also susceptible to MV infection in NHP brain slice cultures. Our findings suggest that MV and CDV have comparable neurotropism and intrinsic capacity to infect CNS-resident cells of their natural host species. |
format | Online Article Text |
id | pubmed-8402773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84027732021-08-29 Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species Laksono, Brigitta M. Tran, Diana N. Kondova, Ivanela van Engelen, Harry G. H. Michels, Samira Nambulli, Sham de Vries, Rory D. Duprex, W. Paul Verjans, Georges M. G. M. de Swart, Rik L. Viruses Article Measles virus (MV) and canine distemper virus (CDV) are closely related members of the family Paramyxoviridae, genus Morbillivirus. MV infection of humans and non-human primates (NHPs) results in a self-limiting disease, which rarely involves central nervous system (CNS) complications. In contrast, infection of carnivores with CDV usually results in severe disease, in which CNS complications are common and the case-fatality rate is high. To compare the neurovirulence and neurotropism of MV and CDV, we established a short-term organotypic brain slice culture system of the olfactory bulb, hippocampus, or cortex obtained from NHPs, dogs, and ferrets. Slices were inoculated ex vivo with wild-type-based recombinant CDV or MV expressing a fluorescent reporter protein. The infection level of both morbilliviruses was determined at different times post-infection. We observed equivalent infection levels and identified microglia as main target cells in CDV-inoculated carnivore and MV-inoculated NHP brain tissue slices. Neurons were also susceptible to MV infection in NHP brain slice cultures. Our findings suggest that MV and CDV have comparable neurotropism and intrinsic capacity to infect CNS-resident cells of their natural host species. MDPI 2021-08-10 /pmc/articles/PMC8402773/ /pubmed/34452447 http://dx.doi.org/10.3390/v13081582 Text en © 2021 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 Laksono, Brigitta M. Tran, Diana N. Kondova, Ivanela van Engelen, Harry G. H. Michels, Samira Nambulli, Sham de Vries, Rory D. Duprex, W. Paul Verjans, Georges M. G. M. de Swart, Rik L. Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species |
title | Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species |
title_full | Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species |
title_fullStr | Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species |
title_full_unstemmed | Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species |
title_short | Comparable Infection Level and Tropism of Measles Virus and Canine Distemper Virus in Organotypic Brain Slice Cultures Obtained from Natural Host Species |
title_sort | comparable infection level and tropism of measles virus and canine distemper virus in organotypic brain slice cultures obtained from natural host species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402773/ https://www.ncbi.nlm.nih.gov/pubmed/34452447 http://dx.doi.org/10.3390/v13081582 |
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