Neuroanatomical abnormalities in a nonhuman primate model of congenital Zika virus infection.
Danielle BeckmanAdele M H SeelkeJeffrey L BennettPaige DoughertyKoen K A Van RompayRebekah KeeslerPatricia A PesaventoLark L A CoffeyJohn H MorrisonEliza Bliss-MoreauPublished in: eLife (2022)
We evaluated neuropathological consequences of fetal ZIKV exposure in rhesus monkeys, a translatable animal model for human neural development, by carrying out quantitative neuroanatomical analyses of the nearly full-term brains of fetuses infected with ZIKV and procedure-matched controls. For each animal, a complete cerebral hemisphere was evaluated using immunohistochemical (IHC) and neuroanatomical techniques to detect virus, identify affected cell types, and evaluate gross neuroanatomical abnormalities. IHC staining revealed the presence of ZIKV in the frontal lobe, which contained activated microglia and showed increased apoptosis of immature neurons. ZIKV-infected animals exhibited macrostructural changes within the visual pathway. Regional differences tracked with the developmental timing of the brain, suggesting inflammatory processes related to viral infiltration swept through the cortex, followed by a wave of cell death resulting in morphological changes. These findings may help explain why some infants born with normal sized heads during the ZIKV epidemic manifest developmental challenges as they age.
Keyphrases
- zika virus
- cell death
- gestational age
- functional connectivity
- oxidative stress
- single cell
- resting state
- cell cycle arrest
- sars cov
- optical coherence tomography
- spinal cord
- preterm infants
- minimally invasive
- stem cells
- inflammatory response
- bone marrow
- cerebral ischemia
- mesenchymal stem cells
- low birth weight
- cell proliferation
- preterm birth
- induced pluripotent stem cells
- children with cerebral palsy