Journal Article

Zika virus targets human trophoblast stem cells and prevents syncytialization in placental trophoblast organoids

Li, Kai, Wang, Hongmei, Li, De-Yu, Wu, Ai-Ping, Wang, Yue, Tian, Ying, Wu, Hao, Sun, Meng-Xu, Zhou, Hang-Yu, He, Beijia, Qin, Cheng-Feng, Huang, Xing-Yao

2023

Overview

Zika virus (ZIKV) infection during pregnancy threatens pregnancy and fetal health. However, the infectivity and pathological effects of ZIKV on placental trophoblast progenitor cells in early human embryos remain largely unknown. Here, using human trophoblast stem cells (hTSCs), we demonstrated that hTSCs were permissive to ZIKV infection, and resistance to ZIKV increased with hTSC differentiation. Combining gene knockout and transcriptome analysis, we demonstrated that the intrinsic expression of AXL and TIM-1 , and the absence of potent interferon (IFN)-stimulated genes (ISGs) and IFNs contributed to the high sensitivity of hTSCs to ZIKV. Furthermore, using our newly developed hTSC-derived trophoblast organoid (hTSC-organoid), we demonstrated that ZIKV infection disrupted the structure of mature hTSC-organoids and inhibited syncytialization. Single-cell RNA sequencing (scRNA-seq) further demonstrated that ZIKV infection of hTSC-organoids disrupted the stemness of hTSCs and the proliferation of cytotrophoblast cells (CTBs) and probably led to a preeclampsia (PE) phenotype. Overall, our results clearly demonstrate that hTSCs represent the major target cells of ZIKV, and a reduced syncytialization may result from ZIKV infection of early developing placenta. These findings deepen our understanding of the characteristics and consequences of ZIKV infection of hTSCs in early human embryos. The pathological effects of Zika virus (ZIKV) infection on placental trophoblast progenitor cells in early human embryos are not well understood. In this study, using human trophoblast stem cells (hTSCs), Wu et al. show that hTSCs are readily infected by ZIKV, but that there is increasing resistance to the virus as differentiation towards mature lineages proceeds.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 38 / 38/91 / 42/100 / 631/326/596/2553 / 631/326/596/2557 / 631/532 / 96/31 / Achievement tests / Axl protein / Cell proliferation / Differentiation / Disease resistance / Embryos / Fetuses / Gene sequencing / Humanities and Social Sciences / Infections / Infectivity / Interferon / multidisciplinary / Organoids / Pathological effects / Phenotypes / Placenta / Pre-eclampsia / Pregnancy / Pregnancy complications / Progenitor cells / Science / Science (multidisciplinary) / Stem cells / Transcriptomes / Vector-borne diseases / Viruses / Zika virus