Quantitative definition of neurobehavior, vision, hearing and brain volumes in macaques congenitally exposed to Zika virus
Author:
Koenig Michelle R.ORCID, Razo Elaina, Mitzey AnnORCID, Newman Christina M.ORCID, Dudley Dawn M.ORCID, Breitbach Meghan E.ORCID, Semler Matthew R., Stewart Laurel M., Weiler Andrea M., Rybarczyk Sierra, Bach Kathryn M., Mohns Mariel S., Simmons Heather A., Mejia AndresORCID, Fritsch Michael, Dennis Maria, Teixeira Leandro B. C.ORCID, Schotzko Michele L., Nork T. Michael, Rasmussen Carol A.ORCID, Katz Alex, Nair Veena, Hou Jiancheng, Hartman Amy, Hoeve James VerORCID, Kim Charlene, Schneider Mary L., Ausderau Karla, Kohn Sarah, Jaeger Anna S., Aliota Matthew T.ORCID, Hayes Jennifer M.ORCID, Schultz-Darken NancyORCID, Eickhoff Jens, Antony Kathleen M.ORCID, Noguchi Kevin, Zeng XiankunORCID, Permar Sallie, Prabhakaran Vivek, Capuano Saverio, Friedrich Thomas C.ORCID, Golos Thaddeus G., O’Connor David H.ORCID, Mohr Emma L.ORCID
Abstract
AbstractCongenital 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.
Publisher
Cold Spring Harbor Laboratory
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