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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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 |
work_keys_str_mv |
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