Department of Pediatrics, Division of Pediatric Infectious Diseases, University of Minnesota, Minneapolis, MN, United States.
Informatics Institute, University of Minnesota, Minneapolis, MN, United States.
Front Immunol. 2021 Jun 15;12:686415. doi: 10.3389/fimmu.2021.686415. eCollection 2021.
Human cytomegalovirus (HCMV) infects the placenta, and these placental infections can cause fetal injury and/or demise. The timing of maternal HCMV infection during pregnancy is a determinant of fetal outcomes, but how development affects the placenta's susceptibility to infection, the likelihood of placental injury post-infection, and the frequency of transplacental HCMV transmission remains unclear. In this study, guinea pig cytomegalovirus (GPCMV) was used to model primary maternal infection and compare the effects of infection at two different times on the placenta. When guinea pigs were infected with GPCMV at either 21- or 35-days gestation (dGA), maternal and placental viral loads, as determined by droplet digital PCR, were not significantly affected by the timing of maternal infection. However, when the transcriptomes of gestational age-matched GPCMV-infected and control placentas were compared, significant infection-associated changes in gene expression were only observed after maternal infection at 35 dGA. Notably, transcripts associated with immune activation (e.g. , , , and ) were upregulated in the infected placenta. A GPCMV-specific hybridization assay detected rare infected cells in the main placenta after maternal infection at either time, and maternal infection at 35 dGA also caused large areas of GPCMV-infected cells in the junctional zone. As GPCMV infection after mid-gestation is known to cause high rates of stillbirth and/or fetal growth restriction, our results suggest that the placenta becomes sensitized to infection-associated injury late in gestation, conferring an increased risk of adverse pregnancy outcomes after cytomegalovirus infection.
人类巨细胞病毒(HCMV)感染胎盘,这些胎盘感染可导致胎儿损伤和/或死亡。孕妇在怀孕期间感染 HCMV 的时间是决定胎儿结局的一个因素,但发育如何影响胎盘对感染的易感性、感染后胎盘损伤的可能性以及 HCMV 通过胎盘传播的频率尚不清楚。在这项研究中,豚鼠巨细胞病毒(GPCMV)被用于模拟母体初次感染,并比较在两个不同时间点感染对胎盘的影响。当豚鼠在妊娠 21 天或 35 天(dGA)时感染 GPCMV 时,通过液滴数字 PCR 确定的母体和胎盘病毒载量不受母体感染时间的显著影响。然而,当比较与妊娠天数匹配的 GPCMV 感染和对照胎盘的转录组时,仅在母体在 35 dGA 时感染后观察到与感染相关的基因表达显著变化。值得注意的是,与免疫激活相关的转录本(例如、、和)在感染的胎盘上调。在母体感染后的任一时间,GPCMV 特异性杂交测定仅在主要胎盘中检测到罕见的感染细胞,而母体在 35 dGA 时的感染也导致连接区中大量 GPCMV 感染的细胞。由于妊娠中期后的 GPCMV 感染已知会导致高比例的死产和/或胎儿生长受限,我们的结果表明,胎盘在妊娠晚期对感染相关损伤变得敏感,增加了巨细胞病毒感染后不良妊娠结局的风险。