“Our results demonstrate that [Zika virus] induces cell death in human iPS-derived neural stem cells, disrupts the formation of neurospheres and reduces the growth of organoids, indicating that [Zika] infection in models that mimics the first trimester of brain development may result in severe damage,” the authors wrote in their study.
Zika virus has been associated with the recent dramatic increase in the number of microcephaly cases in Brazil. While the link has not been proven, previous studies have shown that the virus can infect and kill neural stem cells.
For the present study, Garcez and colleagues coaxed iPSCs to develop into neural stem cells. They infected the neural progenitors with Zika virus and grew them as clusters of cells (neurospheres), and as miniature brain organoids.
After six days, uninfected control cells developed hundreds of neurospheres, whereas only a few of the infected neurospheres survived. In addition, after 11 days, the Zika-infected organoids were about 40 percent smaller than uninfected organoids.
To confirm the effects weren’t a feature of flavivirus infection, the researchers grew neural stem cells infected with dengue virus 2, which is similar to Zika. After six days, many more of the dengue-infected cells survived compared with the Zika-infected ones. And after 11 days, dengue-infected organoids were no smaller than uninfected tissue, the researchers found.
Meanwhile, some scientists are still debating the mechanism by which Zika may cause microcephaly. A paper published earlier this month (March 4) in The Lancet called for further studies to determine whether the birth defect is due to direct infection of brain cells or due to the placenta mounting a response to the virus.