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先天性感染寨卡病毒猕猴的神经行为、视觉、听觉和大脑容量的定量定义。

Quantitative definition of neurobehavior, vision, hearing and brain volumes in macaques congenitally exposed to Zika virus.

机构信息

Department of Pathology and Laboratory Medicine, UW-Madison, Madison, Wisconsin, United States of America.

Department of Comparative Biosciences, UW-Madison, Madison, Wisconsin, United States of America.

出版信息

PLoS One. 2020 Oct 22;15(10):e0235877. doi: 10.1371/journal.pone.0235877. eCollection 2020.

DOI:10.1371/journal.pone.0235877
PMID:33091010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7580995/
Abstract

Congenital Zika virus (ZIKV) exposure results in a spectrum of disease ranging from severe birth defects to delayed onset neurodevelopmental deficits. ZIKV-related neuropathogenesis, predictors of birth defects, and neurodevelopmental deficits are not well defined in people. Here we assess the methodological and statistical feasibility of a congenital ZIKV exposure macaque model for identifying infant neurobehavior and brain abnormalities that may underlie neurodevelopmental deficits. We inoculated five pregnant macaques with ZIKV and mock-inoculated one macaque in the first trimester. Following birth, growth, ocular structure/function, brain structure, hearing, histopathology, and neurobehavior were quantitatively assessed during the first week of life. We identified the typical pregnancy outcomes of congenital ZIKV infection, with fetal demise and placental abnormalities. We estimated sample sizes needed to define differences between groups and demonstrated that future studies quantifying brain region volumes, retinal structure, hearing, and visual pathway function require a sample size of 14 animals per group (14 ZIKV, 14 control) to detect statistically significant differences in at least half of the infant exam parameters. Establishing the parameters for future studies of neurodevelopmental outcomes following congenital ZIKV exposure in macaques is essential for robust and rigorous experimental design.

摘要

先天性寨卡病毒(ZIKV)暴露导致一系列疾病,从严重的出生缺陷到神经发育迟滞。ZIKV 相关的神经发病机制、出生缺陷的预测因子和神经发育迟滞在人群中尚未明确界定。在这里,我们评估了先天性 ZIKV 暴露猕猴模型在识别可能导致神经发育缺陷的婴儿神经行为和大脑异常方面的方法学和统计学可行性。我们用 ZIKV 接种五只怀孕的猕猴,并在妊娠早期用假病毒接种一只猕猴。出生后,在生命的第一周内,我们对生长、眼部结构/功能、大脑结构、听力、组织病理学和神经行为进行了定量评估。我们确定了先天性 ZIKV 感染的典型妊娠结局,包括胎儿死亡和胎盘异常。我们估计了确定组间差异所需的样本量,并表明未来研究定量评估大脑区域体积、视网膜结构、听力和视觉通路功能需要每组 14 只动物(14 只 ZIKV,14 只对照)的样本量,才能检测到至少一半婴儿检查参数的统计学显著差异。在猕猴中建立先天性 ZIKV 暴露后神经发育结局的未来研究参数对于稳健和严格的实验设计至关重要。

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