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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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.
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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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