A cynomolgus macaque model for Crimean–Congo haemorrhagic fever

被引:0
|
作者
Elaine Haddock
Friederike Feldmann
David W. Hawman
Marko Zivcec
Patrick W. Hanley
Greg Saturday
Dana P. Scott
Tina Thomas
Miša Korva
Tatjana Avšič -Županc
David Safronetz
Heinz Feldmann
机构
[1] Laboratory of Virology,Department of Medical Microbiology
[2] Division of Intramural Research,Laboratory for Diagnostics of Zoonoses and WHO Centre, Institute of Microbiology and Immunology, Faculty of Medicine
[3] National Institute of Allergy and Infectious Diseases,undefined
[4] National Institutes of Health,undefined
[5] Rocky Mountain Veterinary Branch,undefined
[6] Division of Intramural Research,undefined
[7] National Institute of Allergy and Infectious Diseases,undefined
[8] National Institutes of Health,undefined
[9] University of Manitoba,undefined
[10] University of Ljubljana,undefined
[11] Viral Special Pathogens Branch,undefined
[12] Centers for Disease Control and Prevention,undefined
[13] Special Pathogens Program,undefined
[14] National Microbiology Laboratory,undefined
[15] Public Health Agency of Canada,undefined
来源
Nature Microbiology | 2018年 / 3卷
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摘要
Crimean–Congo haemorrhagic fever (CCHF) is the most medically significant tick-borne disease, being widespread in the Middle East, Asia, Africa and parts of Europe1. Increasing case numbers, westerly movement and broadly ranging case fatality rates substantiate the concern of CCHF as a public health threat. Ixodid ticks of the genus Hyalomma are the vector for CCHF virus (CCHFV), an arbovirus in the genus Orthonairovirus of the family Nairoviridae. CCHFV naturally infects numerous wild and domestic animals via tick bite without causing obvious disease2,3. Severe disease occurs only in humans and transmission usually happens through tick bite or contact with infected animals or humans. The only CCHF disease model is a subset of immunocompromised mice4–6. Here, we show that following CCHFV infection, cynomolgus macaques exhibited hallmark signs of human CCHF with remarkably similar viral dissemination, organ pathology and disease progression. Histopathology showed infection of hepatocytes, endothelial cells and monocytes and fatal outcome seemed associated with endothelial dysfunction manifesting in a clinical shock syndrome with coagulopathy. This non-human primate model will be an invaluable asset for CCHFV countermeasures development.
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页码:556 / 562
页数:6
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