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Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection
Helicobacter pylori is a causative pathogen of many gastric and extra-gastric diseases. It has infected about half of the global population. There were no genome-wide association studies (GWAS) for H. pylori infection conducted in Chinese population, who carried different and relatively homogenous s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440747/ https://www.ncbi.nlm.nih.gov/pubmed/34521966 http://dx.doi.org/10.1038/s41598-021-97790-7 |
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author | Hu, Dingxue Lu, Yueqi Wang, Daoming Nie, Chao Li, Yan |
author_facet | Hu, Dingxue Lu, Yueqi Wang, Daoming Nie, Chao Li, Yan |
author_sort | Hu, Dingxue |
collection | PubMed |
description | Helicobacter pylori is a causative pathogen of many gastric and extra-gastric diseases. It has infected about half of the global population. There were no genome-wide association studies (GWAS) for H. pylori infection conducted in Chinese population, who carried different and relatively homogenous strain of H. pylori. In this work, we performed SNP (single nucleotide polymorphism)-based, gene-based and pathway-based genome-wide association analyses to investigate the genetic basis of host susceptibility to H. pylori infection in 480 Chinese individuals. We also profiled the composition and function of the gut microbiota between H. pylori infection cases and controls. We found several genes and pathways associated with H. pylori infection (P < 0.05), replicated one previously reported SNP rs10004195 in TLR1 gene region (P = 0.02). We also found that glycosaminoglycan biosynthesis related pathway was associated with both onset and progression of H. pylori infection. In the gut microbiome association study, we identified 2 species, 3 genera and several pathways had differential abundance between H. pylori infected cases and controls. This paper is the first GWAS for H. pylori infection in Chinese population, and we combined the genetic and microbial data to comprehensively discuss the basis of host susceptibility to H. pylori infection. |
format | Online Article Text |
id | pubmed-8440747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84407472021-09-20 Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection Hu, Dingxue Lu, Yueqi Wang, Daoming Nie, Chao Li, Yan Sci Rep Article Helicobacter pylori is a causative pathogen of many gastric and extra-gastric diseases. It has infected about half of the global population. There were no genome-wide association studies (GWAS) for H. pylori infection conducted in Chinese population, who carried different and relatively homogenous strain of H. pylori. In this work, we performed SNP (single nucleotide polymorphism)-based, gene-based and pathway-based genome-wide association analyses to investigate the genetic basis of host susceptibility to H. pylori infection in 480 Chinese individuals. We also profiled the composition and function of the gut microbiota between H. pylori infection cases and controls. We found several genes and pathways associated with H. pylori infection (P < 0.05), replicated one previously reported SNP rs10004195 in TLR1 gene region (P = 0.02). We also found that glycosaminoglycan biosynthesis related pathway was associated with both onset and progression of H. pylori infection. In the gut microbiome association study, we identified 2 species, 3 genera and several pathways had differential abundance between H. pylori infected cases and controls. This paper is the first GWAS for H. pylori infection in Chinese population, and we combined the genetic and microbial data to comprehensively discuss the basis of host susceptibility to H. pylori infection. Nature Publishing Group UK 2021-09-14 /pmc/articles/PMC8440747/ /pubmed/34521966 http://dx.doi.org/10.1038/s41598-021-97790-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hu, Dingxue Lu, Yueqi Wang, Daoming Nie, Chao Li, Yan Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection |
title | Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection |
title_full | Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection |
title_fullStr | Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection |
title_full_unstemmed | Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection |
title_short | Glycosaminoglycan biosynthesis pathway in host genome is associated with Helicobacter pylori infection |
title_sort | glycosaminoglycan biosynthesis pathway in host genome is associated with helicobacter pylori infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440747/ https://www.ncbi.nlm.nih.gov/pubmed/34521966 http://dx.doi.org/10.1038/s41598-021-97790-7 |
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