Genome-wide CRISPR screen for Zika virus resistance in human neural cells.
Yun LiJulien MuffatAttya Omer JavedHeather R KeysTenzin LungjangwaIrene BoschMehreen KhanMaria C VirgilioLee GehrkeDavid M SabatiniRudolf JaenischPublished in: Proceedings of the National Academy of Sciences of the United States of America (2019)
Zika virus (ZIKV) is a neurotropic and neurovirulent arbovirus that has severe detrimental impact on the developing human fetal brain. To date, little is known about the factors required for ZIKV infection of human neural cells. We identified ZIKV host genes in human pluripotent stem cell (hPSC)-derived neural progenitors (NPs) using a genome-wide CRISPR-Cas9 knockout screen. Mutations of host factors involved in heparan sulfation, endocytosis, endoplasmic reticulum processing, Golgi function, and interferon activity conferred resistance to infection with the Uganda strain of ZIKV and a more recent North American isolate. Host genes essential for ZIKV replication identified in human NPs also provided a low level of protection against ZIKV in isogenic human astrocytes. Our findings provide insights into host-dependent mechanisms for ZIKV infection in the highly vulnerable human NP cells and identify molecular targets for potential therapeutic intervention.
Keyphrases
- zika virus
- endothelial cells
- genome wide
- crispr cas
- dengue virus
- stem cells
- induced pluripotent stem cells
- pluripotent stem cells
- induced apoptosis
- aedes aegypti
- randomized controlled trial
- endoplasmic reticulum
- genome editing
- multiple sclerosis
- signaling pathway
- cell proliferation
- brain injury
- blood brain barrier
- copy number
- single cell