| Literature DB >> 30192975 |
Colm Atkins1, Jinxin Miao2,3, Birte Kalveram1, Terry Juelich1, Jennifer K Smith1, David Perez1, Lihong Zhang1, Jonna L B Westover2, Arnaud J Van Wettere2, Brian B Gowen2, Zhongde Wang2, Alexander N Freiberg1,4,5.
Abstract
Marburg virus (MARV; family Filoviridae) causes sporadic outbreaks of Marburg hemorrhagic fever in sub-Saharan Africa with case fatality rates reaching 90%. Wild-type filoviruses, including MARV and the closely related Ebola virus, are unable to suppress the type I interferon response in rodents, and therefore require adaptation of the viruses to cause disease in immunocompetent animals. In the current study, we demonstrate that STAT2 knockout Syrian hamsters are susceptible to infection with different wild-type MARV variants. MARV Musoke causes a robust and systemic infection resulting in lethal disease. Histopathological findings share features similar to those observed in human patients and other animal models of filovirus infection. Reverse-transcription polymerase chain reaction analysis of host transcripts shows a dysregulation of the innate immune response. Our results demonstrate that the STAT2 knockout hamster represents a novel small animal model of severe MARV infection and disease without the requirement for virus adaptation.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30192975 PMCID: PMC6249581 DOI: 10.1093/infdis/jiy457
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226