Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Shuwen, Han, Yinhang, Wu, Xingming, Zhao, Jing, Zhuang, Jinxin, Liu, Wei, Wu, Kefeng, Ding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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
_version_ 1784860325183488000
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
work_keys_str_mv AT shuwenhan usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography
AT yinhangwu usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography
AT xingmingzhao usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography
AT jingzhuang usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography
AT jinxinliu usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography
AT weiwu usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography
AT kefengding usingwholegenomesequencingwgstoplotcolorectalcancerrelatedgutmicrobiotainapopulationwithvariedgeography