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Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography
BACKGROUND: Colorectal cancer (CRC) is a multifactorial disease with genetic and environmental factors. Regional differences in risk factors are an important reason for the different incidences of CRC in different regions. OBJECTIVE: The goal was to clarify the intestinal microbial composition and s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795735/ https://www.ncbi.nlm.nih.gov/pubmed/36578080 http://dx.doi.org/10.1186/s13099-022-00524-x |
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author | Shuwen, Han Yinhang, Wu Xingming, Zhao Jing, Zhuang Jinxin, Liu Wei, Wu Kefeng, Ding |
author_facet | Shuwen, Han Yinhang, Wu Xingming, Zhao Jing, Zhuang Jinxin, Liu Wei, Wu Kefeng, Ding |
author_sort | Shuwen, Han |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) is a multifactorial disease with genetic and environmental factors. Regional differences in risk factors are an important reason for the different incidences of CRC in different regions. OBJECTIVE: The goal was to clarify the intestinal microbial composition and structure of CRC patients in different regions and construct CRC risk prediction models based on regional differences. METHODS: A metagenomic dataset of 601 samples from 6 countries in the GMrepo and NCBI databases was collected. All whole-genome sequencing (WGS) data were annotated for species by MetaPhlAn2. We obtained the relative abundance of species composition at the species level and genus level. The MicrobiotaProcess package was used to visualize species composition and PCA. LEfSe analysis was used to analyze the differences in the datasets in each region. Spearman correlation analysis was performed for CRC differential species. Finally, the CRC risk prediction model was constructed and verified in each regional dataset. RESULTS: The composition of the intestinal bacterial community varied in different regions. Differential intestinal bacteria of CRC in different regions are inconsistent. There was a common diversity of bacteria in all six countries, such as Peptostreptococcus stomatis and Fusobacterium nucleatum at the species level. Peptostreptococcus stomatis (species level) and Peptostreptococcus (genus level) are important CRC-related bacteria that are related to other bacteria in different regions. Region has little influence on the accuracy of the CRC risk prediction model. Peptostreptococcus stomatis is an important variable in CRC risk prediction models in all regions. CONCLUSION: Peptostreptococcus stomatis is a common high-risk pathogen of CRC worldwide, and it is an important variable in CRC risk prediction models in all regions. However, regional differences in intestinal bacteria had no significant impact on the accuracy of the CRC risk prediction model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-022-00524-x. |
format | Online Article Text |
id | pubmed-9795735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97957352022-12-29 Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography Shuwen, Han Yinhang, Wu Xingming, Zhao Jing, Zhuang Jinxin, Liu Wei, Wu Kefeng, Ding Gut Pathog Research BACKGROUND: Colorectal cancer (CRC) is a multifactorial disease with genetic and environmental factors. Regional differences in risk factors are an important reason for the different incidences of CRC in different regions. OBJECTIVE: The goal was to clarify the intestinal microbial composition and structure of CRC patients in different regions and construct CRC risk prediction models based on regional differences. METHODS: A metagenomic dataset of 601 samples from 6 countries in the GMrepo and NCBI databases was collected. All whole-genome sequencing (WGS) data were annotated for species by MetaPhlAn2. We obtained the relative abundance of species composition at the species level and genus level. The MicrobiotaProcess package was used to visualize species composition and PCA. LEfSe analysis was used to analyze the differences in the datasets in each region. Spearman correlation analysis was performed for CRC differential species. Finally, the CRC risk prediction model was constructed and verified in each regional dataset. RESULTS: The composition of the intestinal bacterial community varied in different regions. Differential intestinal bacteria of CRC in different regions are inconsistent. There was a common diversity of bacteria in all six countries, such as Peptostreptococcus stomatis and Fusobacterium nucleatum at the species level. Peptostreptococcus stomatis (species level) and Peptostreptococcus (genus level) are important CRC-related bacteria that are related to other bacteria in different regions. Region has little influence on the accuracy of the CRC risk prediction model. Peptostreptococcus stomatis is an important variable in CRC risk prediction models in all regions. CONCLUSION: Peptostreptococcus stomatis is a common high-risk pathogen of CRC worldwide, and it is an important variable in CRC risk prediction models in all regions. However, regional differences in intestinal bacteria had no significant impact on the accuracy of the CRC risk prediction model. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-022-00524-x. BioMed Central 2022-12-28 /pmc/articles/PMC9795735/ /pubmed/36578080 http://dx.doi.org/10.1186/s13099-022-00524-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Shuwen, Han Yinhang, Wu Xingming, Zhao Jing, Zhuang Jinxin, Liu Wei, Wu Kefeng, Ding Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography |
title | Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography |
title_full | Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography |
title_fullStr | Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography |
title_full_unstemmed | Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography |
title_short | Using whole-genome sequencing (WGS) to plot colorectal cancer-related gut microbiota in a population with varied geography |
title_sort | using whole-genome sequencing (wgs) to plot colorectal cancer-related gut microbiota in a population with varied geography |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795735/ https://www.ncbi.nlm.nih.gov/pubmed/36578080 http://dx.doi.org/10.1186/s13099-022-00524-x |
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