Knight Jason M, Davidson Laurie A, Herman Damir, Martin Camilia R, Goldsby Jennifer S, Ivanov Ivan V, Donovan Sharon M, Chapkin Robert S
1] Department of Electrical Engineering, Texas A&M University, College Station, TX [2] Center for Translational Environmental Health Research, Texas A&M University, College Station, TX.
1] Department of Nutrition & Food Science, Texas A&M University, College Station, TX [2] Center for Translational Environmental Health Research, Texas A&M University, College Station, TX.
Sci Rep. 2014 Jun 26;4:5453. doi: 10.1038/srep05453.
The state and development of the intestinal epithelium is vital for infant health, and increased understanding in this area has been limited by an inability to directly assess epithelial cell biology in the healthy newborn intestine. To that end, we have developed a novel, noninvasive, molecular approach that utilizes next generation RNA sequencing on stool samples containing intact epithelial cells for the purpose of quantifying intestinal gene expression. We then applied this technique to compare host gene expression in healthy term and extremely preterm infants. Bioinformatic analyses demonstrate repeatable detection of human mRNA expression, and network analysis shows immune cell function and inflammation pathways to be up-regulated in preterm infants. This study provides incontrovertible evidence that whole-genome sequencing of stool-derived RNA can be used to examine the neonatal host epithelial transcriptome in infants, which opens up opportunities for sequential monitoring of gut gene expression in response to dietary or therapeutic interventions.
肠道上皮的状态和发育对婴儿健康至关重要,然而,由于无法直接评估健康新生儿肠道中的上皮细胞生物学特性,该领域的深入了解受到了限制。为此,我们开发了一种新颖的、非侵入性的分子方法,该方法利用下一代RNA测序技术对含有完整上皮细胞的粪便样本进行分析,以量化肠道基因表达。然后,我们应用这项技术比较了足月健康婴儿和极早产儿的宿主基因表达情况。生物信息学分析表明,人类mRNA表达具有可重复性检测,网络分析显示免疫细胞功能和炎症途径在早产儿中上调。这项研究提供了确凿的证据,表明粪便来源RNA的全基因组测序可用于检测婴儿的新生儿宿主上皮转录组,这为响应饮食或治疗干预而对肠道基因表达进行连续监测开辟了机会。