Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis

Gut microbiota appears to be involved in the pathogenesis of primary sclerosing cholangitis (PSC). The protein tyrosine phosphatase nonreceptor 2 (PTPN2) gene risk variant rs1893217 is associated with gut dysbiosis in inflammatory bowel disease (IBD), and PTPN2 was mentioned as a possible risk gene...

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Main Authors: Luisa Denoth, Pascal Juillerat, Andreas E. Kremer, Gerhard Rogler, Michael Scharl, Bahtiyar Yilmaz, Sena Bluemel, on behalf of the Swiss IBD Cohort Study
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Microorganisms
Subjects:
PSC
Online Access:https://www.mdpi.com/2076-2607/9/8/1752
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spelling doaj-2fb0b2b0fc914897a1afc7f35a048be72021-08-26T14:06:04ZengMDPI AGMicroorganisms2076-26072021-08-0191752175210.3390/microorganisms9081752Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative ColitisLuisa Denoth0Pascal Juillerat1Andreas E. Kremer2Gerhard Rogler3Michael Scharl4Bahtiyar Yilmaz5Sena Bluemel6on behalf of the Swiss IBD Cohort StudyDepartment of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zürich, SwitzerlandMaurice Müller Laboratories, Department for Biomedical Research, University of Bern, 3012 Bern, SwitzerlandDepartment of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zürich, SwitzerlandDepartment of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zürich, SwitzerlandDepartment of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zürich, SwitzerlandMaurice Müller Laboratories, Department for Biomedical Research, University of Bern, 3012 Bern, SwitzerlandDepartment of Gastroenterology and Hepatology, University Hospital Zurich, Rämistrasse 100, 8091 Zürich, SwitzerlandGut microbiota appears to be involved in the pathogenesis of primary sclerosing cholangitis (PSC). The protein tyrosine phosphatase nonreceptor 2 (PTPN2) gene risk variant rs1893217 is associated with gut dysbiosis in inflammatory bowel disease (IBD), and PTPN2 was mentioned as a possible risk gene for PSC. This study assessed the microbial profile of ulcerative colitis (UC) patients with PSC and without PSC (non-PSC). Additionally, effects of the PTPN2 risk variant were assessed. In total, 216 mucosal samples from ileum, colon, and rectum were collected from 7 PSC and 42 non-PSC patients, as well as 28 control subjects (non-IBD). The microbial composition was derived from 16S rRNA sequencing data. Overall, bacterial richness was highest in PSC patients, who also had a higher relative abundance of the genus <i>Roseburia</i> compared to non-PSC, as well as <i>Haemophilus</i>, <i>Fusobacterium</i>, <i>Bifidobacterium,</i> and <i>Actinobacillus</i> compared to non-IBD, as well as a lower relative abundance of <i>Bacteroides</i> compared to non-PSC and non-IBD, respectively. After exclusion of patients with the PTPN2 risk variant, <i>Brachyspira</i> was higher in PSC compared to non-PSC, while, solely in colon samples, <i>Eubacterium</i> and <i>Tepidimonas</i> were higher in PSC vs. non-IBD. In conclusion, this study underlines the presence of gut mucosa-associated microbiome changes in PSC patients and rather weakens the role of PTPN2 as a PSC risk gene.https://www.mdpi.com/2076-2607/9/8/1752PSCPTPN2TCPTPmucosa-associated microbiome<i>Roseburia</i><i>Tepidimonas</i>
collection DOAJ
language English
format Article
sources DOAJ
author Luisa Denoth
Pascal Juillerat
Andreas E. Kremer
Gerhard Rogler
Michael Scharl
Bahtiyar Yilmaz
Sena Bluemel
on behalf of the Swiss IBD Cohort Study
spellingShingle Luisa Denoth
Pascal Juillerat
Andreas E. Kremer
Gerhard Rogler
Michael Scharl
Bahtiyar Yilmaz
Sena Bluemel
on behalf of the Swiss IBD Cohort Study
Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis
Microorganisms
PSC
PTPN2
TCPTP
mucosa-associated microbiome
<i>Roseburia</i>
<i>Tepidimonas</i>
author_facet Luisa Denoth
Pascal Juillerat
Andreas E. Kremer
Gerhard Rogler
Michael Scharl
Bahtiyar Yilmaz
Sena Bluemel
on behalf of the Swiss IBD Cohort Study
author_sort Luisa Denoth
title Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis
title_short Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis
title_full Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis
title_fullStr Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis
title_full_unstemmed Modulation of the Mucosa-Associated Microbiome Linked to the PTPN2 Risk Gene in Patients with Primary Sclerosing Cholangitis and Ulcerative Colitis
title_sort modulation of the mucosa-associated microbiome linked to the ptpn2 risk gene in patients with primary sclerosing cholangitis and ulcerative colitis
publisher MDPI AG
series Microorganisms
issn 2076-2607
publishDate 2021-08-01
description Gut microbiota appears to be involved in the pathogenesis of primary sclerosing cholangitis (PSC). The protein tyrosine phosphatase nonreceptor 2 (PTPN2) gene risk variant rs1893217 is associated with gut dysbiosis in inflammatory bowel disease (IBD), and PTPN2 was mentioned as a possible risk gene for PSC. This study assessed the microbial profile of ulcerative colitis (UC) patients with PSC and without PSC (non-PSC). Additionally, effects of the PTPN2 risk variant were assessed. In total, 216 mucosal samples from ileum, colon, and rectum were collected from 7 PSC and 42 non-PSC patients, as well as 28 control subjects (non-IBD). The microbial composition was derived from 16S rRNA sequencing data. Overall, bacterial richness was highest in PSC patients, who also had a higher relative abundance of the genus <i>Roseburia</i> compared to non-PSC, as well as <i>Haemophilus</i>, <i>Fusobacterium</i>, <i>Bifidobacterium,</i> and <i>Actinobacillus</i> compared to non-IBD, as well as a lower relative abundance of <i>Bacteroides</i> compared to non-PSC and non-IBD, respectively. After exclusion of patients with the PTPN2 risk variant, <i>Brachyspira</i> was higher in PSC compared to non-PSC, while, solely in colon samples, <i>Eubacterium</i> and <i>Tepidimonas</i> were higher in PSC vs. non-IBD. In conclusion, this study underlines the presence of gut mucosa-associated microbiome changes in PSC patients and rather weakens the role of PTPN2 as a PSC risk gene.
topic PSC
PTPN2
TCPTP
mucosa-associated microbiome
<i>Roseburia</i>
<i>Tepidimonas</i>
url https://www.mdpi.com/2076-2607/9/8/1752
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