Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, 1 Shields Avenue, Davis, CA, 95616, USA.
California National Primate Research Center, University of California, 1 Shields Avenue, Davis, CA, 95616, USA.
Nat Commun. 2018 Jun 20;9(1):2414. doi: 10.1038/s41467-018-04777-6.
Zika virus (ZIKV) infection of pregnant women can cause fetal microcephaly and other neurologic defects. We describe the development of a non-human primate model to better understand fetal pathogenesis. To reliably induce fetal infection at defined times, four pregnant rhesus macaques are inoculated intravenously and intraamniotically with ZIKV at gestational day (GD) 41, 50, 64, or 90, corresponding to first and second trimester of gestation. The GD41-inoculated animal, experiencing fetal death 7 days later, has high virus levels in fetal and placental tissues, implicating ZIKV as cause of death. The other three fetuses are carried to near term and euthanized; while none display gross microcephaly, all show ZIKV RNA in many tissues, especially in the brain, which exhibits calcifications and reduced neural precursor cells. Given that this model consistently recapitulates neurologic defects of human congenital Zika syndrome, it is highly relevant to unravel determinants of fetal neuropathogenesis and to explore interventions.
寨卡病毒(ZIKV)感染孕妇可导致胎儿小头畸形和其他神经系统缺陷。我们描述了一种非人类灵长类动物模型的建立,以便更好地了解胎儿发病机制。为了在特定时间可靠地诱导胎儿感染,我们在妊娠第 41、50、64 和 90 天(对应妊娠的第一和第二 trimester)时,通过静脉内和羊膜内途径对四只怀孕的恒河猴接种 ZIKV。在第 41 天接种的动物 7 天后发生胎儿死亡,其胎儿和胎盘组织中的病毒水平很高,提示 ZIKV 是导致死亡的原因。另外三只胎儿被带到接近足月并被安乐死;虽然没有一只表现出明显的小头畸形,但所有胎儿的许多组织中都显示出 ZIKV RNA,尤其是大脑,大脑显示出钙化和神经前体细胞减少。鉴于该模型始终重现人类先天性寨卡综合征的神经缺陷,它对于阐明胎儿神经发病机制的决定因素以及探索干预措施非常重要。