Vincent Caroline, Mehrotra Sudeep, Loo Vivian G, Dewar Ken, Manges Amee R
Department of Microbiology and Immunology, McGill University, Montreal, QC, Canada H3A 2B4 ; McGill University and Génome Québec Innovation Centre, Montreal, QC, Canada H3A 0G1.
McGill University and Génome Québec Innovation Centre, Montreal, QC, Canada H3A 0G1 ; Department of Human Genetics, McGill University, Montreal, QC, Canada H3A 1B1.
J Immunol Res. 2015;2015:246203. doi: 10.1155/2015/246203. Epub 2015 May 18.
Clostridium difficile infection (CDI) is intricately linked to the health of the gastrointestinal tract and its indigenous microbiota. In this study, we assessed whether fecal excretion of host DNA is associated with CDI development. Assuming that shedding of epithelial cell increases in the inflamed intestine, we used human DNA excretion as a marker of intestinal insult. Whole-genome shotgun sequencing was employed to quantify host DNA excretion and evaluate bacterial content in fecal samples collected from patients with incipient CDI, hospitalized controls, and healthy subjects. Human DNA excretion was significantly increased in patients admitted to the hospital for a gastrointestinal ailment, as well as prior to an episode of CDI. In multivariable analyses, human read abundance was independently associated with CDI development. Host DNA proportions were negatively correlated with intestinal microbiota diversity. Enterococcus and Escherichia were enriched in patients excreting high quantities of human DNA, while Ruminococcus and Odoribacter were depleted. These findings suggest that intestinal inflammation can occur prior to CDI development and may influence patient susceptibility to CDI. The quantification of human DNA in feces could serve as a simple and noninvasive approach to assess bowel inflammation and identify patients at risk of CDI.
艰难梭菌感染(CDI)与胃肠道及其固有微生物群的健康密切相关。在本研究中,我们评估了宿主DNA的粪便排泄是否与CDI的发生有关。假设炎症肠道中上皮细胞脱落增加,我们将人类DNA排泄用作肠道损伤的标志物。采用全基因组鸟枪法测序来量化宿主DNA排泄,并评估从初发性CDI患者、住院对照和健康受试者收集的粪便样本中的细菌含量。因胃肠道疾病入院的患者以及CDI发作前,人类DNA排泄显著增加。在多变量分析中,人类读数丰度与CDI的发生独立相关。宿主DNA比例与肠道微生物群多样性呈负相关。在排泄大量人类DNA的患者中,肠球菌和大肠杆菌富集,而瘤胃球菌和气味杆菌减少。这些发现表明,肠道炎症可能在CDI发生之前出现,并可能影响患者对CDI的易感性。粪便中人类DNA的定量可作为一种简单且无创的方法来评估肠道炎症,并识别有CDI风险的患者。