Postnatal Zika virus infection leads to morphological and cellular alterations within the neurogenic niche.
Jéssica C C G FerreiraRaissa Rilo ChristoffTailene RabelloRaiane Oliveira FerreiraCarolina BatistaPedro Junior Pinheiro MourãoÁtila D RossiLuiza Mendonça HigaMaria BellioAmilcar TanuriPatricia Pestana GarcezPublished in: Disease models & mechanisms (2024)
The Zika virus received significant attention in 2016, following a declaration by the World Health Organization of an epidemic in the Americas, in which infections were associated with microcephaly. Indeed, prenatal Zika virus infection is detrimental to fetal neural stem cells and can cause premature cell loss and neurodevelopmental abnormalities in newborn infants, collectively described as congenital Zika syndrome. Contrastingly, much less is known about how neonatal infection affects the development of the newborn nervous system. Here, we investigated the development of the dentate gyrus of wild-type mice following intracranial injection of the virus at birth (postnatal day 0). Through this approach, we found that Zika virus infection affected the development of neurogenic regions within the dentate gyrus and caused reactive gliosis, cell death and a decrease in cell proliferation. Such infection also altered volumetric features of the postnatal dentate gyrus. Thus, we found that Zika virus exposure to newborn mice is detrimental to the subgranular zone of the dentate gyrus. These observations offer insight into the cellular mechanisms that underlie the neurological features of congenital Zika syndrome in children.
Keyphrases
- zika virus
- dengue virus
- wild type
- aedes aegypti
- cell death
- cell proliferation
- preterm infants
- spinal cord injury
- young adults
- pregnant women
- single cell
- high fat diet induced
- stem cells
- cell cycle
- cell therapy
- type diabetes
- autism spectrum disorder
- skeletal muscle
- mesenchymal stem cells
- subarachnoid hemorrhage
- brain injury