Characterization of the Gut Microbiota and Mycobiota in Italian Pediatric Patients With Primary Sclerosing Cholangitis and Ulcerative Colitis

被引:9
作者
Del Chierico, Federica [1 ,5 ]
Cardile, Sabrina [2 ]
Baldelli, Valerio [1 ]
Alterio, Tommaso [2 ]
Reddel, Sofia [1 ]
Bramuzzo, Matteo [3 ]
Knafelz, Daniela [2 ]
Lega, Sara [3 ]
Bracci, Fiammetta [2 ]
Torre, Giuliano [2 ]
Maggiore, Giuseppe [2 ]
Putignani, Lorenza [4 ]
机构
[1] Bambino Gesu Pediat Hosp, Unit Human Microbiome, Immunol Rheumatol & Infect Dis Res Area, IRCCS, Rome, Italy
[2] Bambino Gesu Childrens Hosp IRCCS, Hepatol Gastroenterol Nutr & Liver transplantat Un, Hepatol Gastroenterol Liver Transplantat Unit, Rome, Italy
[3] Inst Maternal & Child Hlth, Gastroenterol Digest Endoscopy & Nutr Unit, IRCCS Burlo Garofolo, Trieste, Italy
[4] Bambino Gesu Pediat Hosp, Unit Microbiol & Diagnost Immunol, Unit Microbi & Immunol, Unit Human Microbiome,Rheumatol & Infect Dis Res A, Rome, Italy
[5] Viale San Paolo 15, I-00146 Rome, Italy
关键词
primary sclerosing cholangitis; ulcerative colitis; gut microbiota; gut mycobiota; dysbiosis; DYSBIOSIS; GENE; BILE;
D O I
10.1093/ibd/izad203
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Primary sclerosing cholangitis (PSC) is a chronic, fibroinflammatory, cholestatic liver disease of unknown etiopathogenesis, often associated with inflammatory bowel diseases. Recent evidence ascribes, together with immunologic and environmental components, a significant role to the intestinal microbiota or its molecules in the PSC pathogenesis.Methods By metagenomic sequencing of 16S rRNA and ITS2 loci, we describe the fecal microbiota and mycobiota of 26 pediatric patients affected by PSC and concomitant ulcerative colitis (PSC-UC), 27 patients without PSC but with UC (UC), and 26 healthy subjects (CTRLs).Results Compared with CTRL, the bacterial and fungal gut dysbiosis was evident for both PSC-UC and UC groups; in particular, Streptococcus, Saccharomyces, Sporobolomyces, Tilletiopsis, and Debaryomyces appeared increased in PSC-UC, whereas Klebsiella, Haemophilus, Enterococcus Collinsella, Piptoporus, Candida, and Hyphodontia in UC. In both patient groups, Akkermansia, Bacteroides, Parabacteroides, Oscillospira, Meyerozyma and Malassezia were decreased. Co-occurrence analysis evidenced the lowest number of nodes and edges for fungi networks compared with bacteria. Finally, we identified a specific patient profile, based on liver function tests, bacterial and fungal signatures, that is able to distinguish PSC-UC from UC patients.Conclusions We describe the gut microbiota and mycobiota dysbiosis associated to PSC-UC disease. Our results evidenced a gut imbalance, with the reduction of gut commensal microorganisms with stated anti-inflammatory properties (ie, Akkermansia, Bacteroides, Parabacteroides, Oscillospira, Meyerozyma, and Malassezia) and the increase of pathobionts (ie, Streptococcus, Saccharomyces, and Debaryomyces) that could be involved in PSC progression. Altogether, these events may concur in the pathophysiology of PSC in the framework of UC. In this study, we report the gut microbiota and mycobiota dysbiosis in pediatric patients affected by primary sclerosing cholangitis (PSC) associated with ulcerative colitis (UC), with an increase in pro-inflammatory pathobionts and a reduction in anti-inflammatory commensals.
引用
收藏
页码:529 / 537
页数:9
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