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Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice
The common small animal disease models for Zika virus (ZIKV) are mice lacking the interferon responses, but infection of interferon receptor α/β knock out (IFNAR(−/−)) mice is not uniformly lethal particularly in older animals. Here we sought to advance this model in regard to lethality for future c...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904210/ https://www.ncbi.nlm.nih.gov/pubmed/29696134 http://dx.doi.org/10.3389/fcimb.2018.00117 |
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author | Marzi, Andrea Emanuel, Jackson Callison, Julie McNally, Kristin L. Arndt, Nicolette Chadinha, Spencer Martellaro, Cynthia Rosenke, Rebecca Scott, Dana P. Safronetz, David Whitehead, Stephen S. Best, Sonja M. Feldmann, Heinz |
author_facet | Marzi, Andrea Emanuel, Jackson Callison, Julie McNally, Kristin L. Arndt, Nicolette Chadinha, Spencer Martellaro, Cynthia Rosenke, Rebecca Scott, Dana P. Safronetz, David Whitehead, Stephen S. Best, Sonja M. Feldmann, Heinz |
author_sort | Marzi, Andrea |
collection | PubMed |
description | The common small animal disease models for Zika virus (ZIKV) are mice lacking the interferon responses, but infection of interferon receptor α/β knock out (IFNAR(−/−)) mice is not uniformly lethal particularly in older animals. Here we sought to advance this model in regard to lethality for future countermeasure efficacy testing against more recent ZIKV strains from the Asian lineage, preferably the American sublineage. We first infected IFNAR(−/−) mice subcutaneously with the contemporary ZIKV-Paraiba strain resulting in predominantly neurological disease with ~50% lethality. Infection with ZIKV-Paraiba by different routes established a uniformly lethal model only in young mice (4-week old) upon intraperitoneal infection. However, intraperitoneal inoculation of ZIKV-French Polynesia resulted in uniform lethality in older IFNAR(−/−) mice (10–12-weeks old). In conclusion, we have established uniformly lethal mouse disease models for efficacy testing of antivirals and vaccines against recent ZIKV strains representing the Asian lineage. |
format | Online Article Text |
id | pubmed-5904210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59042102018-04-25 Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice Marzi, Andrea Emanuel, Jackson Callison, Julie McNally, Kristin L. Arndt, Nicolette Chadinha, Spencer Martellaro, Cynthia Rosenke, Rebecca Scott, Dana P. Safronetz, David Whitehead, Stephen S. Best, Sonja M. Feldmann, Heinz Front Cell Infect Microbiol Microbiology The common small animal disease models for Zika virus (ZIKV) are mice lacking the interferon responses, but infection of interferon receptor α/β knock out (IFNAR(−/−)) mice is not uniformly lethal particularly in older animals. Here we sought to advance this model in regard to lethality for future countermeasure efficacy testing against more recent ZIKV strains from the Asian lineage, preferably the American sublineage. We first infected IFNAR(−/−) mice subcutaneously with the contemporary ZIKV-Paraiba strain resulting in predominantly neurological disease with ~50% lethality. Infection with ZIKV-Paraiba by different routes established a uniformly lethal model only in young mice (4-week old) upon intraperitoneal infection. However, intraperitoneal inoculation of ZIKV-French Polynesia resulted in uniform lethality in older IFNAR(−/−) mice (10–12-weeks old). In conclusion, we have established uniformly lethal mouse disease models for efficacy testing of antivirals and vaccines against recent ZIKV strains representing the Asian lineage. Frontiers Media S.A. 2018-04-11 /pmc/articles/PMC5904210/ /pubmed/29696134 http://dx.doi.org/10.3389/fcimb.2018.00117 Text en Copyright © 2018 Marzi, Emanuel, Callison, McNally, Arndt, Chadinha, Martellaro, Rosenke, Scott, Safronetz, Whitehead, Best and Feldmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Marzi, Andrea Emanuel, Jackson Callison, Julie McNally, Kristin L. Arndt, Nicolette Chadinha, Spencer Martellaro, Cynthia Rosenke, Rebecca Scott, Dana P. Safronetz, David Whitehead, Stephen S. Best, Sonja M. Feldmann, Heinz Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice |
title | Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice |
title_full | Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice |
title_fullStr | Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice |
title_full_unstemmed | Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice |
title_short | Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice |
title_sort | lethal zika virus disease models in young and older interferon α/β receptor knock out mice |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904210/ https://www.ncbi.nlm.nih.gov/pubmed/29696134 http://dx.doi.org/10.3389/fcimb.2018.00117 |
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