Fungi participate in the dysbiosis of gut microbiota in patients with primary sclerosing cholangitis

被引:165
作者
Lemoinne, Sara [1 ,2 ,3 ]
Kemgang, Astrid [1 ,2 ,3 ]
Ben Belkacem, Karima [1 ,2 ,3 ]
Straube, Marjolene [1 ,4 ]
Jegou, Sarah [1 ,4 ]
Corpechot, Christophe [1 ,2 ,3 ]
Chazouilleres, Olivier [1 ,2 ,3 ]
Housset, Chantal [1 ,2 ,3 ]
Sokol, Harry [1 ,4 ,5 ]
Lionel, Arrive
Laurent, Beaugerie
Anne, Bourrier
Marine, Camus
ChafaiNajim
Edouard, Chambenois
ChaputUlriikka
Charlotte, Delattre
Chloe, Martineau
Laurence, Cholley Monnier
DeboveClotilde
Xavier, Dray
Jean-Francois, Flejou
Guillaume, Le Gall
Nadia, Hoyeau
Julien, Kirchgesner
Cecilia, Landman
LevevreJeremie
Philippe, Marteau
Isabelle, Nion-Larmurier
Violaine, Ozenne
Yann, Parc
Philippe, Seksik
Harry, Sokol
Magali, Svrcek
机构
[1] Sorbonne Univ, INSERM, CRSA, Paris, France
[2] Sorbonne Univ, INSERM, ICAN, Paris, France
[3] Hop St Antoine, AP HP, Reference Ctr Inflammatory Biliary Dis & Autoimmu, Dept Hepatol, Paris, France
[4] Hop St Antoine, AP HP, Dept Gastroenterol, F-75012 Paris, France
[5] AgroParisTech, INRA, UMR1319 Micalis, Jouy En Josas, France
关键词
MUCOSA-ASSOCIATED MICROBIOTA; INFLAMMATORY-BOWEL-DISEASE; INTESTINAL MICROBIOTA; INSULIN SENSITIVITY; LIVER; PROFILES;
D O I
10.1136/gutjnl-2018-317791
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Patients with primary sclerosing cholangitis (PSC) were previously shown to display a bacterial gut dysbiosis but fungal microbiota has never been examined in these patients. The aim of this study was to assess the fungal gut microbiota in patients with PSC. Design We analysed the faecal microbiota of patients with PSC and concomitant IBD (n=27), patients with PSC and no IBD (n=22), patients with IBD and no PSC (n=33) and healthy subjects (n=30). Bacterial and fungal composition of the faecal microbiota was determined using 16S and ITS2 sequencing, respectively. Results We found that patients with PSC harboured bacterial dysbiosis characterised by a decreased biodiversity, an altered composition and a decreased correlation network density. These alterations of the microbiota were associated with PSC, independently of IBD status. For the first time, we showed that patients with PSC displayed a fungal gut dysbiosis, characterised by a relative increase in biodiversity and an altered composition. Notably, we observed an increased proportion of Exophiala and a decreased proportion of Saccharomyces cerevisiae. Compared with patients with IBD and healthy subjects, the gut microbiota of patients with PSC exhibited a strong disruption in bacteria-fungi correlation network, suggesting an alteration in the interkingdom crosstalk. Conclusion This study demonstrates that bacteria and fungi contribute to gut dysbiosis in PSC.
引用
收藏
页码:92 / 102
页数:11
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