怀孕
转录组
免疫系统
微生物群
生物
核糖核酸
免疫学
病毒载量
病毒
基因组
基因
生物信息学
基因表达
遗传学
作者
Wenying Pan,Thuy T. M. Ngo,Joan Camuñas-Soler,Chun‐Xiao Song,Mark Kowarsky,Yair J. Blumenfeld,Ronald J. Wong,Gary M. Shaw,David K. Stevenson,Stephen R. Quake
出处
期刊:Clinical Chemistry
[American Association for Clinical Chemistry]
日期:2017-09-13
卷期号:63 (11): 1695-1704
被引量:70
标识
DOI:10.1373/clinchem.2017.273888
摘要
Abstract BACKGROUND Plasma cell-free RNA (cfRNA) encompasses a broad spectrum of RNA species that can be derived from both human cells and microbes. Because cfRNA is fragmented and of low concentration, it has been challenging to profile its transcriptome using standard RNA-seq methods. METHODS We assessed several recently developed RNA-seq methods on cfRNA samples. We then analyzed the dynamic changes of both the human transcriptome and the microbiome of plasma during pregnancy from 60 women. RESULTS cfRNA reflects a well-orchestrated immune modulation during pregnancy: an up-regulation of antiinflammatory genes and an increased abundance of antimicrobial genes. We observed that the plasma microbiome remained relatively stable during pregnancy. The bacteria Ureaplasma shows an increased prevalence and increased abundance at postpartum, which is likely to be associated with postpartum infection. We demonstrated that cfRNA-seq can be used to monitor viral infections. We detected a number of human pathogens in our patients, including an undiagnosed patient with a high load of human parvovirus B19 virus (B19V), which is known to be a potential cause of complications in pregnancy. CONCLUSIONS Plasma cfRNA-seq demonstrates the potential to simultaneously monitor immune response and microbial infections during pregnancy.
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