Bray M, Davis K, Geisbert T, Schmaljohn C, Huggins J
Division of Virology, US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland 21702-5011, USA.
J Infect Dis. 1998 Sep;178(3):651-61. doi: 10.1086/515386.
The Zaire subtype of Ebola virus (EBO-Z) is lethal for newborn mice, but adult mice are resistant to the virus, which prevents their use as an animal model of lethal Ebola infection. We serially passed EBO-Z virus in progressively older suckling mice, eventually obtaining a plaque-purified virus that was lethal for mature, immunocompetent BALB/c and C57BL/6 inbred and ICR (CD-1) outbred mice. Pathologic changes in the liver and spleen of infected mice resembled those in EBO-Z-infected primates. Virus titers in these tissues reached 10(9) pfu/g. The LD50 of mouse-adapted EBO-Z virus inoculated into the peritoneal cavity was approximately 1 virion. Mice were resistant to large doses of the same virus inoculated subcutaneously, intradermally, or intramuscularly. Mice injected peripherally with mouse-adapted or intraperitoneally with non-adapted EBO-Z virus resisted subsequent challenge with mouse-adapted virus.
埃博拉病毒扎伊尔亚型(EBO-Z)对新生小鼠具有致死性,但成年小鼠对该病毒具有抗性,这使得它们无法用作致死性埃博拉感染的动物模型。我们在逐渐长大的乳鼠中连续传代EBO-Z病毒,最终获得了一种经噬斑纯化的病毒,该病毒对成熟的、具有免疫能力的BALB/c和C57BL/6近交系小鼠以及ICR(CD-1)远交系小鼠具有致死性。感染小鼠肝脏和脾脏的病理变化与EBO-Z感染的灵长类动物相似。这些组织中的病毒滴度达到10(9) pfu/g。腹腔接种适应小鼠的EBO-Z病毒的半数致死剂量约为1个病毒粒子。小鼠对皮下、皮内或肌肉注射大剂量的相同病毒具有抗性。外周注射适应小鼠的EBO-Z病毒或腹腔注射未适应的EBO-Z病毒的小鼠对随后适应小鼠的病毒攻击具有抗性。