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Hantavirus infection in type I interferon receptor-deficient (A129) mice
Type I interferon receptor knockout mice (strain A129) were assessed as a disease model of hantavirus infection. A range of infection routes (intramuscular, intraperitoneal and intranasal) were assessed using minimally passaged Seoul virus (strain Humber). Dissemination of virus to the spleen, kidne...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660455/ https://www.ncbi.nlm.nih.gov/pubmed/32667279 http://dx.doi.org/10.1099/jgv.0.001470 |
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author | Dowall, Stuart D. Graham, Victoria A. Aram, Marilyn Findlay-Wilson, Stephen Salguero, Francisco J. Emery, Kirsty Hewson, Roger |
author_facet | Dowall, Stuart D. Graham, Victoria A. Aram, Marilyn Findlay-Wilson, Stephen Salguero, Francisco J. Emery, Kirsty Hewson, Roger |
author_sort | Dowall, Stuart D. |
collection | PubMed |
description | Type I interferon receptor knockout mice (strain A129) were assessed as a disease model of hantavirus infection. A range of infection routes (intramuscular, intraperitoneal and intranasal) were assessed using minimally passaged Seoul virus (strain Humber). Dissemination of virus to the spleen, kidney and lung was observed at 5 days after intramuscular and intraperitoneal challenge, which was resolved by day 14. In contrast, intranasal challenge of A129 mice demonstrated virus tropism to the lung, which was maintained to day 14 post-challenge. These data support the use of the A129 mouse model for future infection studies and the in vivo evaluation of interventions. |
format | Online Article Text |
id | pubmed-7660455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-76604552020-11-13 Hantavirus infection in type I interferon receptor-deficient (A129) mice Dowall, Stuart D. Graham, Victoria A. Aram, Marilyn Findlay-Wilson, Stephen Salguero, Francisco J. Emery, Kirsty Hewson, Roger J Gen Virol Research Article Type I interferon receptor knockout mice (strain A129) were assessed as a disease model of hantavirus infection. A range of infection routes (intramuscular, intraperitoneal and intranasal) were assessed using minimally passaged Seoul virus (strain Humber). Dissemination of virus to the spleen, kidney and lung was observed at 5 days after intramuscular and intraperitoneal challenge, which was resolved by day 14. In contrast, intranasal challenge of A129 mice demonstrated virus tropism to the lung, which was maintained to day 14 post-challenge. These data support the use of the A129 mouse model for future infection studies and the in vivo evaluation of interventions. Microbiology Society 2020-10 2020-07-15 /pmc/articles/PMC7660455/ /pubmed/32667279 http://dx.doi.org/10.1099/jgv.0.001470 Text en © 2020 Crown Copyright http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License. |
spellingShingle | Research Article Dowall, Stuart D. Graham, Victoria A. Aram, Marilyn Findlay-Wilson, Stephen Salguero, Francisco J. Emery, Kirsty Hewson, Roger Hantavirus infection in type I interferon receptor-deficient (A129) mice |
title | Hantavirus infection in type I interferon receptor-deficient (A129) mice |
title_full | Hantavirus infection in type I interferon receptor-deficient (A129) mice |
title_fullStr | Hantavirus infection in type I interferon receptor-deficient (A129) mice |
title_full_unstemmed | Hantavirus infection in type I interferon receptor-deficient (A129) mice |
title_short | Hantavirus infection in type I interferon receptor-deficient (A129) mice |
title_sort | hantavirus infection in type i interferon receptor-deficient (a129) mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660455/ https://www.ncbi.nlm.nih.gov/pubmed/32667279 http://dx.doi.org/10.1099/jgv.0.001470 |
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