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Establishment of a lethal mouse model of emerging tick-borne orthonairovirus infections.
Ariizumi, Takuma; Tabata, Koshiro; Itakura, Yukari; Kobayashi, Hiroko; Hall, William W; Sasaki, Michihito; Sawa, Hirofumi; Matsuno, Keita; Orba, Yasuko.
Afiliação
  • Ariizumi T; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Tabata K; Institute for Vaccine Research and Development, Hokkaido University, Sapporo, Japan.
  • Itakura Y; Institute for Vaccine Research and Development, Hokkaido University, Sapporo, Japan.
  • Kobayashi H; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Hall WW; Institute for Vaccine Research and Development, Hokkaido University, Sapporo, Japan.
  • Sasaki M; National Virus Reference Laboratory, University College Dublin, Belfield, Dublin, 4, Ireland.
  • Sawa H; Global Virus Network, Baltimore, Maryland, United States of America.
  • Matsuno K; International Collaboration Unit, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
  • Orba Y; Division of Molecular Pathobiology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
PLoS Pathog ; 20(3): e1012101, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38502642
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nairovirus / Doenças Transmitidas por Carrapatos Limite: Animals Idioma: En Revista: PLoS Pathog Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nairovirus / Doenças Transmitidas por Carrapatos Limite: Animals Idioma: En Revista: PLoS Pathog Ano de publicação: 2024 Tipo de documento: Article