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A hamster model for Marburg virus infection accurately recapitulates Marburg hemorrhagic fever.
- Source :
-
Scientific reports [Sci Rep] 2016 Dec 15; Vol. 6, pp. 39214. Date of Electronic Publication: 2016 Dec 15. - Publication Year :
- 2016
-
Abstract
- Marburg virus (MARV), a close relative of Ebola virus, is the causative agent of a severe human disease known as Marburg hemorrhagic fever (MHF). No licensed vaccine or therapeutic exists to treat MHF, and MARV is therefore classified as a Tier 1 select agent and a category A bioterrorism agent. In order to develop countermeasures against this severe disease, animal models that accurately recapitulate human disease are required. Here we describe the development of a novel, uniformly lethal Syrian golden hamster model of MHF using a hamster-adapted MARV variant Angola. Remarkably, this model displayed almost all of the clinical features of MHF seen in humans and non-human primates, including coagulation abnormalities, hemorrhagic manifestations, petechial rash, and a severely dysregulated immune response. This MHF hamster model represents a powerful tool for further dissecting MARV pathogenesis and accelerating the development of effective medical countermeasures against human MHF.
- Subjects :
- Animals
Blood Coagulation Disorders etiology
Chlorocebus aethiops
Cricetinae
Cytokines genetics
Cytokines metabolism
Disease Models, Animal
Fibrinogen analysis
Hemorrhage etiology
Immunity, Innate
Kaplan-Meier Estimate
Liver pathology
Marburg Virus Disease immunology
Marburg Virus Disease mortality
Marburg Virus Disease virology
Marburgvirus genetics
Marburgvirus isolation & purification
Mutation
Partial Thromboplastin Time
Prothrombin Time
RNA, Viral genetics
RNA, Viral isolation & purification
RNA, Viral metabolism
Spleen pathology
Vero Cells
Marburg Virus Disease pathology
Marburgvirus pathogenicity
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 6
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 27976688
- Full Text :
- https://doi.org/10.1038/srep39214