TY - JOUR
T1 - The effect of Zika virus infection in the ferret
AU - Hutchinson, Elizabeth B.
AU - Chatterjee, Mitali
AU - Reyes, Laura
AU - Djankpa, Francis T.
AU - Valiant, William G.
AU - Dardzinski, Bernard
AU - Mattapallil, Joseph J.
AU - Pierpaoli, Carlo
AU - Juliano, Sharon L.
N1 - Publisher Copyright:
© 2019 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals, Inc.
PY - 2019/7/1
Y1 - 2019/7/1
N2 - Although initial observations of infections with the Zika virus describe a mild illness, more recent reports show that infections by Zika result in neurotropism. In 2015, substantial congenital malformations were observed, with numerous infants born with microcephaly in Brazil. To study the underlying mechanism and effects of the disease, it is critical to find suitable animal models. Rodents lack an immune system parallel to humans and also have lissencephalic brains, which are likely to react differently to infections. As the smallest gyrencephalic mammal, ferrets may provide an important animal model to study the Zika virus, as their brains share many characteristics with humans. To evaluate the prospect of using ferrets to study Zika virus infection, we injected seven pregnant jills with the PR strain subcutaneously on gestational day 21, corresponding to the initiation of corticogenesis. These injections resulted in mixed effects. Two animals died of apparent infection, and all kits were resorbed in another animal that did not die. The other four animals remained pregnant until gestational day 40, when the kits were delivered by caesarian section. We evaluated the animals using CT, MRI, diffusion tensor imaging, and immunohistochemistry. The kits displayed a number of features compatible with an infection that impacted both the brain and skull. The outcomes, however, were variable and differed within and across litters, which ranged from the absence of observable abnormalities to prominent changes, suggesting differential vulnerability of kits to infection by the Zika virus or to subsequent mechanisms of neurodevelopmental disruption.
AB - Although initial observations of infections with the Zika virus describe a mild illness, more recent reports show that infections by Zika result in neurotropism. In 2015, substantial congenital malformations were observed, with numerous infants born with microcephaly in Brazil. To study the underlying mechanism and effects of the disease, it is critical to find suitable animal models. Rodents lack an immune system parallel to humans and also have lissencephalic brains, which are likely to react differently to infections. As the smallest gyrencephalic mammal, ferrets may provide an important animal model to study the Zika virus, as their brains share many characteristics with humans. To evaluate the prospect of using ferrets to study Zika virus infection, we injected seven pregnant jills with the PR strain subcutaneously on gestational day 21, corresponding to the initiation of corticogenesis. These injections resulted in mixed effects. Two animals died of apparent infection, and all kits were resorbed in another animal that did not die. The other four animals remained pregnant until gestational day 40, when the kits were delivered by caesarian section. We evaluated the animals using CT, MRI, diffusion tensor imaging, and immunohistochemistry. The kits displayed a number of features compatible with an infection that impacted both the brain and skull. The outcomes, however, were variable and differed within and across litters, which ranged from the absence of observable abnormalities to prominent changes, suggesting differential vulnerability of kits to infection by the Zika virus or to subsequent mechanisms of neurodevelopmental disruption.
KW - CT
KW - diffusion tensor MRI
KW - microcephaly
KW - neural development
KW - neural progenitor
KW - RRID:AB_11217435
KW - RRID:AB_234119
KW - RRID:AB_609914
KW - RRID:AB_726362
KW - vasculature
UR - http://www.scopus.com/inward/record.url?scp=85061588504&partnerID=8YFLogxK
U2 - 10.1002/cne.24640
DO - 10.1002/cne.24640
M3 - Article
C2 - 30680733
AN - SCOPUS:85061588504
SN - 0021-9967
VL - 527
SP - 1706
EP - 1719
JO - Journal of Comparative Neurology
JF - Journal of Comparative Neurology
IS - 10
ER -