Department of Cell and Tissue Biology, School of Dentistry, University of California San Francisco.
Division of Infectious Disease and Vaccinology, School of Public Health, University of California Berkeley.
J Infect Dis. 2018 Mar 28;217(8):1202-1213. doi: 10.1093/infdis/jix552.
Maternal Zika virus (ZIKV) infection with prolonged viremia leads to fetal infection and congenital Zika syndrome. Previously, we reported that ZIKV infects primary cells from human placentas and fetal membranes. Here, we studied viral replication in numerous explants of anchoring villi and basal decidua from first-trimester human placentas and midgestation amniotic epithelial cells (AmEpCs).
Explants and AmEpCs were infected with American and African ZIKV strains at low multiplicities, and ZIKV proteins were visualized by immunofluorescence. Titers of infectious progeny, cell proliferation, and invasiveness were quantified.
In anchoring villus, ZIKV replicated reproducibly in proliferating cytotrophoblasts in proximal cell columns, dividing Hofbauer cells in villus cores, and invasive cytotrophoblasts, but frequencies differed. Cytotrophoblasts in explants infected by Nicaraguan strains were invasive, whereas those infected by prototype MR766 largely remained in cell columns, and titers varied by donor and strain. In basal decidua, ZIKV replicated in glandular epithelium, decidual cells, and immune cells. ZIKV-infected AmEpCs frequently occurred in pairs and expressed Ki67 and phosphohistone H3, indicating replication in dividing cells.
ZIKV infection in early pregnancy could target proliferating cell column cytotrophoblasts and Hofbauer cells, amplifying infection in basal decidua and chorionic villi and enabling transplacental transmission.
母体寨卡病毒(ZIKV)感染伴长期病毒血症可导致胎儿感染和先天性寨卡综合征。此前,我们报道寨卡病毒可感染来自人胎盘和胎膜的原代细胞。在此,我们研究了来自孕早期胎盘锚定绒毛和基底蜕膜的众多绒毛附着体和中孕期羊膜上皮细胞(AmEpCs)的病毒复制情况。
用低倍数将胎盘和 AmEpCs 与美洲和非洲 ZIKV 株共孵育,并用免疫荧光法观察 ZIKV 蛋白。定量分析感染性后代的滴度、细胞增殖和侵袭性。
在锚定绒毛中,ZIKV 可在近侧细胞柱中的增殖性细胞滋养层细胞、绒毛核心中的分裂型豪夫伯细胞和侵袭性细胞滋养层细胞中重复复制,但频率不同。尼加拉瓜株感染的绒毛附着体中的滋养层细胞具有侵袭性,而原型 MR766 株感染的滋养层细胞则主要保留在细胞柱中,滴度因供体和株而异。在基底蜕膜中,ZIKV 可在腺上皮细胞、蜕膜细胞和免疫细胞中复制。ZIKV 感染的 AmEpCs 常成对出现,并表达 Ki67 和磷酸组蛋白 H3,表明在分裂细胞中进行复制。
妊娠早期的 ZIKV 感染可能会靶向增殖的细胞柱滋养层细胞和豪夫伯细胞,从而放大基底蜕膜和绒毛的感染,并实现胎盘传播。