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Crimean-Congo Hemorrhagic Fever in Humanized Mice Reveals Glial Cells as Primary Targets of Neurological Infection
Author(s) -
Jessica R. Spengler,
M. Kelly Keating,
Anita K. McElroy,
Marko Zivcec,
JoAnn D. Coleman-McCray,
Jessica R. Harmon,
Brigid C. Bollweg,
Cynthia S. Goldsmith,
Éric Bergeron,
James Keck,
Sherif R. Zaki,
Stuart T. Nichol,
Christina F. Spiropoulou
Publication year - 2017
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/jix215
Subject(s) - crimean–congo hemorrhagic fever , humanized mouse , meningoencephalitis , immunology , disease , gliosis , virology , medicine , biology , meningitis , pathology , immune system , psychiatry
Crimean-Congo hemorrhagic fever (CCHF) is a tick-borne viral hemorrhagic disease seen exclusively in humans. Central nervous system (CNS) infection and neurological involvement have also been reported in CCHF. In the current study, we inoculated NSG-SGM3 mice engrafted with human hematopoietic CD34+ stem cells with low-passage CCHF virus strains isolated from human patients. In humanized mice, lethal disease develops, characterized by histopathological change in the liver and brain. To date, targets of neurological infection and disease have not been investigated in CCHF. CNS disease in humanized mice was characterized by gliosis, meningitis, and meningoencephalitis, and glial cells were identified as principal targets of infection. Humanized mice represent a novel lethal model for studies of CCHF countermeasures, and CCHF-associated CNS disease. Our data suggest a role for astrocyte dysfunction in neurological disease and identify key regions of infection in the CNS for future investigations of CCHF.

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