Linthorst Jasper, Baksi Moezammin M M, Welkers Matthijs R A, Sistermans Erik A
Department of Human Genetics, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Amsterdam Reproduction & Development, Amsterdam, The Netherlands.
Prenat Diagn. 2023 Apr;43(4):448-456. doi: 10.1002/pd.6143. Epub 2022 Apr 27.
Viral infections during pregnancy are a major health concern to mother and fetus. By repurposing cell-free Non Invasive Prenatal Testing (NIPT) sequencing data, we investigated prevalence and abundance of viral DNA in a cohort of 108,349 pregnant women.
Cell-free DNA (cfDNA) sequencing reads that did not map to any of the human chromosomes or mitochondrial DNA of the human reference genome build GRCh38 were aligned to 224 DNA viruses selected from the NCBI refseq viral database.
In total 443,665 reads of viral origin were detected across 42,273 samples representing 165 viral species. Several are known to be potentially harmful during pregnancy and/or childbirth, including Cytomegalovirus, Parvovirus B19 and Hepatitis B. Viral sequences were mostly detected at very low abundance. However, several cases had exceptionally high viral loads for Parvovirus B19, Hepatitis B and others. We found statistically significant associations between presence of viral DNA and gestational age, maternal age, fetal fraction, cfDNA concentration and others.
We demonstrate the feasibility to detect viral DNA from typical genome-wide NIPT cfDNA sequencing and describe the main characteristics of the viral DNA in our cohort. Our dataset of detected viral sequence reads is made publicly available to guide future clinical implementations.
孕期病毒感染是影响母亲和胎儿健康的主要问题。通过重新利用游离DNA无创产前检测(NIPT)测序数据,我们调查了108349名孕妇队列中病毒DNA的流行情况和丰度。
将未映射到人类参考基因组构建GRCh38的任何人类染色体或线粒体DNA的游离DNA(cfDNA)测序读数与从NCBI refseq病毒数据库中选择的224种DNA病毒进行比对。
在代表165种病毒的42273个样本中,共检测到443665条病毒来源的读数。其中几种病毒已知在孕期和/或分娩期间具有潜在危害,包括巨细胞病毒、细小病毒B19和乙型肝炎病毒。病毒序列大多以极低的丰度被检测到。然而,有几例细小病毒B19、乙型肝炎病毒和其他病毒的病毒载量异常高。我们发现病毒DNA的存在与孕周、产妇年龄、胎儿游离DNA比例、cfDNA浓度等之间存在统计学上的显著关联。
我们证明了从典型的全基因组NIPT cfDNA测序中检测病毒DNA的可行性,并描述了我们队列中病毒DNA的主要特征。我们检测到的病毒序列读数数据集已公开提供,以指导未来的临床应用。