Quantitative Medical Imaging Section, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, Maryland.
Department of Anatomy Physiology and Genetics, Bethesda, Maryland.
J Comp Neurol. 2019 Jul 1;527(10):1706-1719. doi: 10.1002/cne.24640. Epub 2019 Feb 15.
Although initial observations of infections with the Zika virus describe a mild illness, more recent reports show that infections by Zika result in neurotropism. In 2015, substantial congenital malformations were observed, with numerous infants born with microcephaly in Brazil. To study the underlying mechanism and effects of the disease, it is critical to find suitable animal models. Rodents lack an immune system parallel to humans and also have lissencephalic brains, which are likely to react differently to infections. As the smallest gyrencephalic mammal, ferrets may provide an important animal model to study the Zika virus, as their brains share many characteristics with humans. To evaluate the prospect of using ferrets to study Zika virus infection, we injected seven pregnant jills with the PR strain subcutaneously on gestational day 21, corresponding to the initiation of corticogenesis. These injections resulted in mixed effects. Two animals died of apparent infection, and all kits were resorbed in another animal that did not die. The other four animals remained pregnant until gestational day 40, when the kits were delivered by caesarian section. We evaluated the animals using CT, MRI, diffusion tensor imaging, and immunohistochemistry. The kits displayed a number of features compatible with an infection that impacted both the brain and skull. The outcomes, however, were variable and differed within and across litters, which ranged from the absence of observable abnormalities to prominent changes, suggesting differential vulnerability of kits to infection by the Zika virus or to subsequent mechanisms of neurodevelopmental disruption.
尽管最初对寨卡病毒感染的观察描述为轻度疾病,但最近的报告显示,寨卡病毒感染可导致神经嗜性。2015 年,巴西大量婴儿出生时出现小头畸形,这是明显的先天畸形。为了研究疾病的潜在机制和影响,找到合适的动物模型至关重要。啮齿动物缺乏与人类平行的免疫系统,并且大脑也为脑回脑,这可能会对感染产生不同的反应。作为最小的脑回哺乳动物,雪貂可能为研究寨卡病毒提供重要的动物模型,因为它们的大脑与人脑有许多共同特征。为了评估使用雪貂研究寨卡病毒感染的前景,我们在妊娠第 21 天经皮给 7 只妊娠母雪貂注射 PR 株,这对应于皮质发生的开始。这些注射产生了混合效应。两只动物死于明显的感染,另一只未死亡的动物的所有幼仔都被吸收。其他四只动物继续妊娠直至妊娠第 40 天,此时通过剖腹产分娩幼仔。我们使用 CT、MRI、扩散张量成像和免疫组织化学评估动物。幼仔表现出许多与影响大脑和颅骨的感染一致的特征。然而,结果是可变的,并且在同一窝和不同窝之间存在差异,从没有观察到明显异常到明显变化不等,这表明幼仔对寨卡病毒感染或随后的神经发育障碍机制的易感性存在差异。