Establishment of a lethal mouse model of emerging tick-borne orthonairovirus infections.
Takuma AriizumiKoshiro TabataYukari ItakuraHiroko KobayashiWilliam W HallMichihito SasakiHirofumi SawaKeita MatsunoYasuko OrbaPublished in: PLoS pathogens (2024)
Emerging and reemerging tick-borne virus infections caused by orthonairoviruses (family Nairoviridae), which are genetically distinct from Crimean-Congo hemorrhagic fever virus, have been recently reported in East Asia. Here, we have established a mouse infection model using type-I/II interferon receptor-knockout mice (AG129 mice) both for a better understanding of the pathogenesis of these infections and validation of antiviral agents using Yezo virus (YEZV), a novel orthonairovirus causing febrile illnesses associated with tick bites in Japan and China. YEZV-inoculated AG129 mice developed hepatitis with body weight loss and died by 6 days post infection. Blood biochemistry tests showed elevated liver enzyme levels, similar to YEZV-infected human patients. AG129 mice treated with favipiravir survived lethal YEZV infection, demonstrating the anti-YEZV effect of this drug. The present mouse model will help us better understand the pathogenicity of the emerging tick-borne orthonairoviruses and the development of specific antiviral agents for their treatment.
Keyphrases
- mouse model
- high fat diet induced
- weight loss
- quantum dots
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- endothelial cells
- highly efficient
- bariatric surgery
- dendritic cells
- type diabetes
- peritoneal dialysis
- staphylococcus aureus
- pseudomonas aeruginosa
- visible light
- skeletal muscle
- body mass index
- adverse drug
- biofilm formation
- pluripotent stem cells