Cargando…
Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas
Recent reports have suggested that the gut microbiota is involved in the progression of colorectal cancer (CRC). The composition of gut microbiota in CRC precursors has not been adequately described. To characterize the structure of adherent microbiota in this disease, we conducted pyrosequencing-ba...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872055/ https://www.ncbi.nlm.nih.gov/pubmed/27194068 http://dx.doi.org/10.1038/srep26337 |
_version_ | 1782432669257170944 |
---|---|
author | Lu, Yingying Chen, Jing Zheng, Junyuan Hu, Guoyong Wang, Jingjing Huang, Chunlan Lou, Lihong Wang, Xingpeng Zeng, Yue |
author_facet | Lu, Yingying Chen, Jing Zheng, Junyuan Hu, Guoyong Wang, Jingjing Huang, Chunlan Lou, Lihong Wang, Xingpeng Zeng, Yue |
author_sort | Lu, Yingying |
collection | PubMed |
description | Recent reports have suggested that the gut microbiota is involved in the progression of colorectal cancer (CRC). The composition of gut microbiota in CRC precursors has not been adequately described. To characterize the structure of adherent microbiota in this disease, we conducted pyrosequencing-based analysis of 16S rRNA genes to determine the bacterial profile of normal colons (healthy controls) and colorectal adenomas (CRC precursors). Adenoma mucosal biopsy samples and adjacent normal colonic mucosa from 31 patients with adenomas and 20 healthy volunteers were profiled using the Illumina MiSeq platform. Principal coordinate analysis (PCoA) showed structural segregation between colorectal adenomatous tissue and control tissue. Alpha diversity estimations revealed higher microbiota diversity in samples from patients with adenomas. Taxonomic analysis illustrated that abundance of eight phyla (Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, Chloroflexi, Cyanobacteria, Candidate-division TM7, and Tenericutes) was significantly different. In addition, Lactococcus and Pseudomonas were enriched in preneoplastic tissue, whereas Enterococcus, Bacillus, and Solibacillus were reduced. However, both PCoA and cluster tree analyses showed similar microbiota structure between adenomatous and adjacent non-adenoma tissues. These present findings provide preliminary experimental evidence supporting that colorectal preneoplastic lesion may be the most important factor leading to alterations in bacterial community composition. |
format | Online Article Text |
id | pubmed-4872055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48720552016-06-01 Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas Lu, Yingying Chen, Jing Zheng, Junyuan Hu, Guoyong Wang, Jingjing Huang, Chunlan Lou, Lihong Wang, Xingpeng Zeng, Yue Sci Rep Article Recent reports have suggested that the gut microbiota is involved in the progression of colorectal cancer (CRC). The composition of gut microbiota in CRC precursors has not been adequately described. To characterize the structure of adherent microbiota in this disease, we conducted pyrosequencing-based analysis of 16S rRNA genes to determine the bacterial profile of normal colons (healthy controls) and colorectal adenomas (CRC precursors). Adenoma mucosal biopsy samples and adjacent normal colonic mucosa from 31 patients with adenomas and 20 healthy volunteers were profiled using the Illumina MiSeq platform. Principal coordinate analysis (PCoA) showed structural segregation between colorectal adenomatous tissue and control tissue. Alpha diversity estimations revealed higher microbiota diversity in samples from patients with adenomas. Taxonomic analysis illustrated that abundance of eight phyla (Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, Chloroflexi, Cyanobacteria, Candidate-division TM7, and Tenericutes) was significantly different. In addition, Lactococcus and Pseudomonas were enriched in preneoplastic tissue, whereas Enterococcus, Bacillus, and Solibacillus were reduced. However, both PCoA and cluster tree analyses showed similar microbiota structure between adenomatous and adjacent non-adenoma tissues. These present findings provide preliminary experimental evidence supporting that colorectal preneoplastic lesion may be the most important factor leading to alterations in bacterial community composition. Nature Publishing Group 2016-05-19 /pmc/articles/PMC4872055/ /pubmed/27194068 http://dx.doi.org/10.1038/srep26337 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lu, Yingying Chen, Jing Zheng, Junyuan Hu, Guoyong Wang, Jingjing Huang, Chunlan Lou, Lihong Wang, Xingpeng Zeng, Yue Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
title | Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
title_full | Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
title_fullStr | Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
title_full_unstemmed | Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
title_short | Mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
title_sort | mucosal adherent bacterial dysbiosis in patients with colorectal adenomas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872055/ https://www.ncbi.nlm.nih.gov/pubmed/27194068 http://dx.doi.org/10.1038/srep26337 |
work_keys_str_mv | AT luyingying mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT chenjing mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT zhengjunyuan mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT huguoyong mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT wangjingjing mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT huangchunlan mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT loulihong mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT wangxingpeng mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas AT zengyue mucosaladherentbacterialdysbiosisinpatientswithcolorectaladenomas |