Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Computational Radiology Laboratory, Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Cell. 2018 May 17;173(5):1111-1122.e10. doi: 10.1016/j.cell.2018.03.019. Epub 2018 Mar 29.
The development of interventions to prevent congenital Zika syndrome (CZS) has been limited by the lack of an established nonhuman primate model. Here we show that infection of female rhesus monkeys early in pregnancy with Zika virus (ZIKV) recapitulates many features of CZS in humans. We infected 9 pregnant monkeys with ZIKV, 6 early in pregnancy (weeks 6-7 of gestation) and 3 later in pregnancy (weeks 12-14 of gestation), and compared findings with uninfected controls. 100% (6 of 6) of monkeys infected early in pregnancy exhibited prolonged maternal viremia and fetal neuropathology, including fetal loss, smaller brain size, and histopathologic brain lesions, including microcalcifications, hemorrhage, necrosis, vasculitis, gliosis, and apoptosis of neuroprogenitor cells. High-resolution MRI demonstrated concordant lesions indicative of deep gray matter injury. We also observed spinal, ocular, and neuromuscular pathology. Our data show that vascular compromise and neuroprogenitor cell dysfunction are hallmarks of CZS pathogenesis, suggesting novel strategies to prevent and to treat this disease.
先天性寨卡综合征(CZS)预防干预措施的发展受到缺乏已建立的非人类灵长类动物模型的限制。在这里,我们表明,在妊娠早期用寨卡病毒(ZIKV)感染雌性恒河猴可重现人类 CZS 的许多特征。我们用 ZIKV 感染了 9 只怀孕的猴子,6 只在妊娠早期(妊娠 6-7 周),3 只在妊娠晚期(妊娠 12-14 周),并将结果与未感染的对照组进行比较。100%(6/6)在妊娠早期感染的猴子表现出延长的母体病毒血症和胎儿神经病理学,包括胎儿丢失、脑体积较小和组织病理学脑损伤,包括微钙化、出血、坏死、血管炎、神经胶质增生和神经祖细胞凋亡。高分辨率 MRI 显示出与深部灰质损伤一致的病变。我们还观察到了脊髓、眼部和神经肌肉病理学。我们的数据表明,血管损伤和神经祖细胞功能障碍是 CZS 发病机制的标志,这表明了预防和治疗这种疾病的新策略。