Schultz Denise A, Sagartz John E, Huso David L, Buller R Mark L
Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Virology. 2009 Jan 5;383(1):86-92. doi: 10.1016/j.virol.2008.09.025. Epub 2008 Nov 1.
Suitable animal models are needed to study monkeypox virus (MPXV) as human monkeypox clinically resembles smallpox and MPXV is a zoonotic and potential bioterroristic agent. We have demonstrated that a species of African dormice, Graphiurus kelleni, is susceptible to a lethal infection of MPXV and that MPXV replicated in multiple organs of this species. Following intranasal administration, MPXV replicated locally in the nasal mucosa causing necrosis and hemorrhage with subsequent systemic spread to lymph nodes, spleen, liver, and other tissues where it caused severe necrosis and/or hemorrhage leading to death. The dormouse model was validated for testing prophylactic (Dryvax vaccine) and therapeutic (cidofovir) test articles against intranasal challenges with MPXV.
由于人类猴痘在临床上与天花相似,且猴痘病毒是一种人畜共患病原体和潜在的生物恐怖主义病原体,因此需要合适的动物模型来研究猴痘病毒(MPXV)。我们已经证明,一种非洲睡鼠,即凯氏笔尾睡鼠,对MPXV的致死性感染敏感,并且MPXV能在该物种的多个器官中复制。经鼻内给药后,MPXV在鼻黏膜局部复制,导致坏死和出血,随后系统性扩散至淋巴结、脾脏、肝脏和其他组织,在这些组织中引起严重坏死和/或出血,最终导致死亡。该睡鼠模型已通过验证,可用于测试针对MPXV经鼻攻击的预防性(Dryvax疫苗)和治疗性(西多福韦)试验品。