Recent Zika virus (ZIKV) infections have been associated with a range of neurological complications, in particular congenital microcephaly. Human neural progenitor cells (hNPCs) are thought to play an important role in the pathogenesis of microcephaly, and experimental ZIKV infection of hNPCs has been shown to induce cell death. However, the infection efficiency and rate of cell death have varied between studies, which might be related to intrinsic differences between African and Asian lineage ZIKV strains. Therefore, we determined the replication kinetics, including infection efficiency, burst size, and ability to induce cell death, of two Asian and two African ZIKV strains. African ZIKV strains replicated to higher titers in Vero cells, human glioblastoma (U87MG) cells, human neuroblastoma (SK-N-SH) cells, and hNPCs than Asian ZIKV strains. Furthermore, infection with Asian ZIKV strains did not result in significant cell death early after infection, whereas infection with African ZIKV strains resulted in high percentages of cell death in hNPCs. The differences between African and Asian lineage ZIKV strains highlight the importance of including relevant ZIKV strains to study the pathogenesis of congenital microcephaly and caution against extrapolation of experimental data obtained using historical African ZIKV strains to the current outbreak. Finally, the fact that Asian ZIKV strains infect only a minority of cells with a relatively low burst size together with the lack of early cell death induction might contribute to its ability to cause chronic infections within the central nervous system (CNS).

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Keywords African strains, Asian strains, Cell death, Growth kinetics, Human neural progenitor cells, Neuronal cells, One-step growth curve, Pathogenesis, Phenotype, Zika virus
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Journal mSphere
Anfasa, F, Siegers, J.Y, Van Der Kroeg, M, Mumtaz, N. (Noreen), Stalin Raj, V, Vrij, F.M.S, … van Riel, D.A.J. (2017). Phenotypic differences between Asian and African lineage Zika viruses in human neural progenitor cells. mSphere, 2(4). doi:10.1128/mSphere.00292-17