Cancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Divisão de Pesquisa Clínica, Instituto Nacional de Câncer, Rio de Janeiro 20230-130, Brazil.
Cells. 2020 Jan 8;9(1):153. doi: 10.3390/cells9010153.
The Zika virus (ZIKV) is a mosquito-borne Flavivirus and can be transmitted through an infected mosquito bite or through human-to-human interaction by sexual activity, blood transfusion, breastfeeding, or perinatal exposure. After the 2015-2016 outbreak in Brazil, a strong link between ZIKV infection and microcephaly emerged. ZIKV specifically targets human neural progenitor cells, suggesting that proteins encoded by ZIKV bind and inactivate host cell proteins, leading to microcephaly. Here, we present a systematic annotation of interactions between human proteins and the seven non-structural ZIKV proteins corresponding to a Brazilian isolate. The interaction network was generated by combining tandem-affinity purification followed by mass spectrometry with yeast two-hybrid screens. We identified 150 human proteins, involved in distinct biological processes, as interactors to ZIKV non-structural proteins. Our interacting network is composed of proteins that have been previously associated with microcephaly in human genetic disorders and/or animal models. Further, we show that the protein inhibitor of activated STAT1 (PIAS1) interacts with NS5 and modulates its stability. This study builds on previously published interacting networks of ZIKV and genes related to autosomal recessive primary microcephaly to generate a catalog of human cellular targets of ZIKV proteins implicated in processes related to microcephaly in humans. Collectively, these data can be used as a resource for future characterization of ZIKV infection biology and help create a basis for the discovery of drugs that may disrupt the interaction and reduce the health damage to the fetus.
寨卡病毒(ZIKV)是一种蚊媒黄病毒,可以通过受感染的蚊子叮咬或通过性活动、输血、母乳喂养或围产期接触在人与人之间传播。2015-2016 年巴西疫情爆发后,寨卡病毒感染与小头症之间出现了很强的关联。寨卡病毒专门针对人类神经祖细胞,表明寨卡病毒编码的蛋白质结合并失活宿主细胞蛋白质,导致小头症。在这里,我们系统地注释了与巴西分离株对应的七种非结构 ZIKV 蛋白与人蛋白之间的相互作用。通过串联亲和纯化结合酵母双杂交筛选,生成了相互作用网络。我们鉴定了 150 个人类蛋白,这些蛋白参与了不同的生物学过程,是 ZIKV 非结构蛋白的相互作用蛋白。我们的相互作用网络由先前与人类遗传疾病和/或动物模型中的小头症相关的微管蛋白组成。此外,我们表明,激活的 STAT1 蛋白抑制剂(PIAS1)与 NS5 相互作用并调节其稳定性。本研究在之前发表的寨卡病毒和与常染色体隐性原发性小头症相关的基因相互作用网络的基础上,生成了与人类小头症相关的 ZIKV 蛋白涉及的细胞靶标的目录。总的来说,这些数据可用作未来寨卡病毒感染生物学特征的资源,并有助于为发现可能破坏相互作用并减少对胎儿健康损害的药物奠定基础。