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Lethal Zika Virus Disease Models in Young and Older Interferon α/β Receptor Knock Out Mice.
- Source :
-
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2018 Apr 11; Vol. 8, pp. 117. Date of Electronic Publication: 2018 Apr 11 (Print Publication: 2018). - Publication Year :
- 2018
-
Abstract
- 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 <superscript>-/-</superscript> ) 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 <superscript>-/-</superscript> 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 <superscript>-/-</superscript> 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.
- Subjects :
- Aedes
Age Factors
Animals
Cell Line
Chlorocebus aethiops
Female
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Vero Cells
Zika Virus pathogenicity
Zika Virus Infection virology
Disease Models, Animal
Receptor, Interferon alpha-beta genetics
Zika Virus isolation & purification
Zika Virus Infection mortality
Zika Virus Infection pathology
Subjects
Details
- Language :
- English
- ISSN :
- 2235-2988
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Frontiers in cellular and infection microbiology
- Publication Type :
- Academic Journal
- Accession number :
- 29696134
- Full Text :
- https://doi.org/10.3389/fcimb.2018.00117