Fungal microbiota dysbiosis in IBD.
Fungal microbiota dysbiosis in IBD.
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DOI:
10.1136/gutjnl-2015-310746
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发表时间:
2017-06
期刊:
影响因子:
24.5
通讯作者:
Beaugerie L
中科院分区:
文献类型:
--
作者:
Sokol H;Leducq V;Aschard H;Pham HP;Jegou S;Landman C;Cohen D;Liguori G;Bourrier A;Nion-Larmurier I;Cosnes J;Seksik P;Langella P;Skurnik D;Richard ML;Beaugerie L
The bacterial intestinal microbiota plays major roles in human physiology and IBDs. Although some data suggest a role of the fungal microbiota in IBD pathogenesis, the available data are scarce. The aim of our study was to characterise the faecal fungal microbiota in patients with IBD. Bacterial and fungal composition of the faecal microbiota of 235 patients with IBD and 38 healthy subjects (HS) was determined using 16S and ITS2 sequencing, respectively. The obtained sequences were analysed using the Qiime pipeline to assess composition and diversity. Bacterial and fungal taxa associated with clinical parameters were identified using multivariate association with linear models. Correlation between bacterial and fungal microbiota was investigated using Spearman's test and distance correlation. We observed that fungal microbiota is skewed in IBD, with an increased Basidiomycota/Ascomycota ratio, a decreased proportion of Saccharomyces cerevisiae and an increased proportion of Candida albicans compared with HS. We also identified disease-specific alterations in diversity, indicating that a Crohn's disease-specific gut environment may favour fungi at the expense of bacteria. The concomitant analysis of bacterial and fungal microbiota showed a dense and homogenous correlation network in HS but a dramatically unbalanced network in IBD, suggesting the existence of disease-specific inter-kingdom alterations. Besides bacterial dysbiosis, our study identifies a distinct fungal microbiota dysbiosis in IBD characterised by alterations in biodiversity and composition. Moreover, we unravel here disease-specific inter-kingdom network alterations in IBD, suggesting that, beyond bacteria, fungi might also play a role in IBD pathogenesis.
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影响因子:
3.7
作者:
Cáliz R;Canet LM;Lupiañez CB;Canhão H;Escudero A;Filipescu I;Segura-Catena J;Soto-Pino MJ;Expósito-Ruiz M;Ferrer MÁ;García A;Romani L;González-Utrilla A;Vallejo T;Pérez-Pampin E;Hemminki K;Försti A;Collantes E;Fonseca JE;Sainz J
通讯作者:
Sainz J
影响因子:
3.7
作者:
Jawhara S;Habib K;Maggiotto F;Pignede G;Vandekerckove P;Maes E;Dubuquoy L;Fontaine T;Guerardel Y;Poulain D
通讯作者:
Poulain D
DOI:
10.1126/science.1221789
发表时间:
2012-06-08
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Iliev ID;Funari VA;Taylor KD;Nguyen Q;Reyes CN;Strom SP;Brown J;Becker CA;Fleshner PR;Dubinsky M;Rotter JI;Wang HL;McGovern DP;Brown GD;Underhill DM
通讯作者:
Underhill DM
影响因子:
30.3
作者:
Gevers D;Kugathasan S;Denson LA;Vázquez-Baeza Y;Van Treuren W;Ren B;Schwager E;Knights D;Song SJ;Yassour M;Morgan XC;Kostic AD;Luo C;González A;McDonald D;Haberman Y;Walters T;Baker S;Rosh J;Stephens M;Heyman M;Markowitz J;Baldassano R;Griffiths A;Sylvester F;Mack D;Kim S;Crandall W;Hyams J;Huttenhower C;Knight R;Xavier RJ
通讯作者:
Xavier RJ
影响因子:
3.7
作者:
Hoffmann C;Dollive S;Grunberg S;Chen J;Li H;Wu GD;Lewis JD;Bushman FD
通讯作者:
Bushman FD