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High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia
Colorectal cancer (CRC) remains the third most common cancer worldwide, with a growing incidence among young adults. Multiple studies have presented associations between the gut microbiome and CRC, suggesting a link with cancer risk. Although CRC microbiome studies continue to profile larger patient...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707393/ https://www.ncbi.nlm.nih.gov/pubmed/29214046 http://dx.doi.org/10.1038/s41522-017-0040-3 |
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author | Drewes, Julia L. White, James R. Dejea, Christine M. Fathi, Payam Iyadorai, Thevambiga Vadivelu, Jamuna Roslani, April C. Wick, Elizabeth C. Mongodin, Emmanuel F. Loke, Mun Fai Thulasi, Kumar Gan, Han Ming Goh, Khean Lee Chong, Hoong Yin Kumar, Sandip Wanyiri, Jane W. Sears, Cynthia L. |
author_facet | Drewes, Julia L. White, James R. Dejea, Christine M. Fathi, Payam Iyadorai, Thevambiga Vadivelu, Jamuna Roslani, April C. Wick, Elizabeth C. Mongodin, Emmanuel F. Loke, Mun Fai Thulasi, Kumar Gan, Han Ming Goh, Khean Lee Chong, Hoong Yin Kumar, Sandip Wanyiri, Jane W. Sears, Cynthia L. |
author_sort | Drewes, Julia L. |
collection | PubMed |
description | Colorectal cancer (CRC) remains the third most common cancer worldwide, with a growing incidence among young adults. Multiple studies have presented associations between the gut microbiome and CRC, suggesting a link with cancer risk. Although CRC microbiome studies continue to profile larger patient cohorts with increasingly economical and rapid DNA sequencing platforms, few common associations with CRC have been identified, in part due to limitations in taxonomic resolution and differences in analysis methodologies. Complementing these taxonomic studies is the newly recognized phenomenon that bacterial organization into biofilm structures in the mucus layer of the gut is a consistent feature of right-sided (proximal), but not left-sided (distal) colorectal cancer. In the present study, we performed 16S rRNA gene amplicon sequencing and biofilm quantification in a new cohort of patients from Malaysia, followed by a meta-analysis of eleven additional publicly available data sets on stool and tissue-based CRC microbiota using Resphera Insight, a high-resolution analytical tool for species-level characterization. Results from the Malaysian cohort and the expanded meta-analysis confirm that CRC tissues are enriched for invasive biofilms (particularly on right-sided tumors), a symbiont with capacity for tumorigenesis (Bacteroides fragilis), and oral pathogens including Fusobacterium nucleatum, Parvimonas micra, and Peptostreptococcus stomatis. Considered in aggregate, species from the Human Oral Microbiome Database are highly enriched in CRC. Although no detected microbial feature was universally present, their substantial overlap and combined prevalence supports a role for the gut microbiota in a significant percentage (>80%) of CRC cases. |
format | Online Article Text |
id | pubmed-5707393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57073932017-12-06 High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia Drewes, Julia L. White, James R. Dejea, Christine M. Fathi, Payam Iyadorai, Thevambiga Vadivelu, Jamuna Roslani, April C. Wick, Elizabeth C. Mongodin, Emmanuel F. Loke, Mun Fai Thulasi, Kumar Gan, Han Ming Goh, Khean Lee Chong, Hoong Yin Kumar, Sandip Wanyiri, Jane W. Sears, Cynthia L. NPJ Biofilms Microbiomes Article Colorectal cancer (CRC) remains the third most common cancer worldwide, with a growing incidence among young adults. Multiple studies have presented associations between the gut microbiome and CRC, suggesting a link with cancer risk. Although CRC microbiome studies continue to profile larger patient cohorts with increasingly economical and rapid DNA sequencing platforms, few common associations with CRC have been identified, in part due to limitations in taxonomic resolution and differences in analysis methodologies. Complementing these taxonomic studies is the newly recognized phenomenon that bacterial organization into biofilm structures in the mucus layer of the gut is a consistent feature of right-sided (proximal), but not left-sided (distal) colorectal cancer. In the present study, we performed 16S rRNA gene amplicon sequencing and biofilm quantification in a new cohort of patients from Malaysia, followed by a meta-analysis of eleven additional publicly available data sets on stool and tissue-based CRC microbiota using Resphera Insight, a high-resolution analytical tool for species-level characterization. Results from the Malaysian cohort and the expanded meta-analysis confirm that CRC tissues are enriched for invasive biofilms (particularly on right-sided tumors), a symbiont with capacity for tumorigenesis (Bacteroides fragilis), and oral pathogens including Fusobacterium nucleatum, Parvimonas micra, and Peptostreptococcus stomatis. Considered in aggregate, species from the Human Oral Microbiome Database are highly enriched in CRC. Although no detected microbial feature was universally present, their substantial overlap and combined prevalence supports a role for the gut microbiota in a significant percentage (>80%) of CRC cases. Nature Publishing Group UK 2017-11-29 /pmc/articles/PMC5707393/ /pubmed/29214046 http://dx.doi.org/10.1038/s41522-017-0040-3 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Drewes, Julia L. White, James R. Dejea, Christine M. Fathi, Payam Iyadorai, Thevambiga Vadivelu, Jamuna Roslani, April C. Wick, Elizabeth C. Mongodin, Emmanuel F. Loke, Mun Fai Thulasi, Kumar Gan, Han Ming Goh, Khean Lee Chong, Hoong Yin Kumar, Sandip Wanyiri, Jane W. Sears, Cynthia L. High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
title | High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
title_full | High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
title_fullStr | High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
title_full_unstemmed | High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
title_short | High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
title_sort | high-resolution bacterial 16s rrna gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707393/ https://www.ncbi.nlm.nih.gov/pubmed/29214046 http://dx.doi.org/10.1038/s41522-017-0040-3 |
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