Zika-Virus-Encoded NS2A Disrupts Mammalian Cortical Neurogenesis by Degrading Adherens Junction Proteins

Cell Stem Cell. 2017 Sep 7;21(3):349-358.e6. doi: 10.1016/j.stem.2017.07.014. Epub 2017 Aug 17.

Abstract

Zika virus (ZIKV) directly infects neural progenitors and impairs their proliferation. How ZIKV interacts with the host molecular machinery to impact neurogenesis in vivo is not well understood. Here, by systematically introducing individual proteins encoded by ZIKV into the embryonic mouse cortex, we show that expression of ZIKV-NS2A, but not Dengue virus (DENV)-NS2A, leads to reduced proliferation and premature differentiation of radial glial cells and aberrant positioning of newborn neurons. Mechanistically, in vitro mapping of protein-interactomes and biochemical analysis suggest interactions between ZIKA-NS2A and multiple adherens junction complex (AJ) components. Functionally, ZIKV-NS2A, but not DENV-NS2A, destabilizes the AJ complex, resulting in impaired AJ formation and aberrant radial glial fiber scaffolding in the embryonic mouse cortex. Similarly, ZIKA-NS2A, but not DENV-NS2A, reduces radial glial cell proliferation and causes AJ deficits in human forebrain organoids. Together, our results reveal pathogenic mechanisms underlying ZIKV infection in the developing mammalian brain.

Keywords: Zika virus; adherens junction; cortical neurogenesis; flavivirus; human organoid; human protein microarray; microcephaly; neural stem cell; neuronal migration; radial glial cell.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adherens Junctions / metabolism*
  • Animals
  • Cell Differentiation
  • Cell Proliferation
  • Cerebral Cortex / embryology
  • Cerebral Cortex / metabolism*
  • HEK293 Cells
  • Humans
  • Mammals / metabolism*
  • Membrane Proteins / metabolism*
  • Mice
  • Neurogenesis*
  • Neuroglia / pathology
  • Protein Binding
  • Protein Interaction Mapping
  • Proteolysis*
  • Viral Nonstructural Proteins / metabolism*
  • Zika Virus / metabolism*
  • Zika Virus Infection / pathology

Substances

  • Membrane Proteins
  • Viral Nonstructural Proteins