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寨卡病毒的垂直传播导致小鼠后代出现神经紊乱。

Vertical Transmission of the Zika Virus Causes Neurological Disorders in Mouse Offspring.

机构信息

State Key Laboratory of Brain and Cognitive Science, CAS Center for Excellence in Brain Science and Intelligence Technology (Shanghai), Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Sci Rep. 2018 Feb 23;8(1):3541. doi: 10.1038/s41598-018-21894-w.

Abstract

The association between Zika virus (ZIKV) infection and congenital malformations such as microcephaly in infants is a public health emergency. Although various in vivo and in vitro models are used for ZIKV research, few animal models are available for resolving the effects of maternal ZIKV infection on neonatal development. Here, we established an immunocompetent mouse model via intrauterine inoculation. Our results confirmed that ZIKV, but not dengue virus, infection caused spontaneous abortions, brain malformations, ocular abnormalities, spinal cord defects and paralysis in mouse offspring. Aside from microcephaly and hippocampal dysplasia, eye abnormalities, including microphthalmia, thinner optic nerves, damaged retinae, and deficient visual projection, were also observed following ZIKV infection. Moreover, ZIKV-infected offspring showed a loss of alpha motor neurons in the spinal cord and cerebellar malformation, which may cause paralysis. ZIKV also impaired adult neurogenesis in neonatal mice. Due to its intact immunity, our rodent model can be used to systematically evaluate the impact of ZIKV on embryonic and neonatal development and to explore potential therapies.

摘要

寨卡病毒(ZIKV)感染与婴儿小头畸形等先天性畸形的关联是公共卫生紧急事件。虽然有多种体内和体外模型用于寨卡病毒研究,但很少有动物模型可用于解决母体寨卡病毒感染对新生儿发育的影响。在这里,我们通过宫内接种建立了一个免疫功能正常的小鼠模型。我们的结果证实,寨卡病毒而不是登革热病毒感染会导致小鼠后代自然流产、脑畸形、眼部异常、脊髓缺陷和瘫痪。除了小头畸形和海马发育不良外,还观察到眼部异常,包括小眼球、视神经变薄、视网膜损伤和视觉投射不足,这些都是寨卡病毒感染后的表现。此外,感染寨卡病毒的后代表现出脊髓中α运动神经元丧失和小脑畸形,这可能导致瘫痪。寨卡病毒还损害了新生小鼠的成年神经发生。由于我们的啮齿动物模型具有完整的免疫系统,因此可以用于系统评估寨卡病毒对胚胎和新生儿发育的影响,并探索潜在的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4118/5824946/01ae49086598/41598_2018_21894_Fig1_HTML.jpg

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