Excretion of Host DNA in Feces Is Associated with Risk of Clostridium difficile Infection

被引:19
作者
Vincent, Caroline [1 ,2 ,3 ]
Mehrotra, Sudeep [2 ,3 ,4 ]
Loo, Vivian G. [5 ]
Dewar, Ken [2 ,3 ,4 ,5 ]
Manges, Amee R. [6 ]
机构
[1] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Montreal, PQ H3A 0G1, Canada
[3] Genome Quebec Innovat Ctr, Montreal, PQ H3A 0G1, Canada
[4] McGill Univ, Dept Human Genet, Montreal, PQ H3A 1B1, Canada
[5] McGill Univ, Ctr Hlth, Res Inst, Montreal, PQ H3H 2R9, Canada
[6] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC V6T 1Z3, Canada
基金
加拿大健康研究院;
关键词
GUT MICROBIOTA; DEOXYRIBONUCLEIC-ACID; FECAL EXCRETION; DISEASE; HEALTH;
D O I
10.1155/2015/246203
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:7
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