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Characterization of a murine model of non-lethal, symptomatic dengue virus infection.
- Source :
-
Scientific reports [Sci Rep] 2018 Mar 20; Vol. 8 (1), pp. 4900. Date of Electronic Publication: 2018 Mar 20. - Publication Year :
- 2018
-
Abstract
- The mosquito-borne disease dengue is caused by four serologically- and genetically-related viruses, termed DENV-1 to DENV-4. Historical setbacks due to lack of human-like mouse models of dengue were partially remedied with characterization of lethal DENV-2 infection in immunocompromised AG129 mice (deficient in IFN-α/β/γ receptors). Recently, our group established lethal AG129 mouse infection models of DENV-1, DENV-3, and DENV-4 using human isolates. Here we compare a non-lethal, disseminated model of DENV-3 infection using strain D83-144 to that of the lethal outcome following infection by strain C0360/94. Both strains belong to DENV-3 genotype II and differ by only 13 amino acids. Intraperitoneal inoculation of AG129 mice with strain D83-144 led to clinical signs of dengue infection, such as cytokine induction, thrombocytopenia, and systemic infection. However, C0360/94 infection led to features of severe human dengue, including coagulopathy and lethal outcome, whereas D83-144 infection does not. This study is the first to investigate a low passage, non-mouse lethal strain in AG129 mice and demonstrates that D83-144 infection induces milder features of human dengue than those induced by lethal C0360/94 infection. The results suggest that the AG129 mouse model has applications to investigate factors associated with mild or severe disease.
- Subjects :
- Animals
Cytokines metabolism
Dengue virology
Disseminated Intravascular Coagulation
Female
Humans
Immunocompromised Host
Male
Mice
Mice, 129 Strain
Mice, Transgenic
Receptors, Interferon deficiency
Serogroup
Thrombocytopenia
Dengue physiopathology
Dengue Virus physiology
Disease Models, Animal
Genotype
RNA, Viral genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 29559699
- Full Text :
- https://doi.org/10.1038/s41598-018-22618-w