Fusobacterium is associated with colorectal adenomas.

The human gut microbiota is increasingly recognized as a player in colorectal cancer (CRC). While particular imbalances in the gut microbiota have been linked to colorectal adenomas and cancer, no specific bacterium has been identified as a risk factor. Recent studies have reported a high abundance...

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Main Authors: Amber N McCoy, Félix Araújo-Pérez, Andrea Azcárate-Peril, Jen Jen Yeh, Robert S Sandler, Temitope O Keku
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3546075?pdf=render
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spelling doaj-f73e636a59a541d0ac23a99d2e6707c62020-11-25T01:00:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5365310.1371/journal.pone.0053653Fusobacterium is associated with colorectal adenomas.Amber N McCoyFélix Araújo-PérezAndrea Azcárate-PerilJen Jen YehRobert S SandlerTemitope O KekuThe human gut microbiota is increasingly recognized as a player in colorectal cancer (CRC). While particular imbalances in the gut microbiota have been linked to colorectal adenomas and cancer, no specific bacterium has been identified as a risk factor. Recent studies have reported a high abundance of Fusobacterium in CRC subjects compared to normal subjects, but this observation has not been reported for adenomas, CRC precursors. We assessed the abundance of Fusobacterium species in the normal rectal mucosa of subjects with (n = 48) and without adenomas (n = 67). We also confirmed previous reports on Fusobacterium and CRC in 10 CRC tumor tissues and 9 matching normal tissues by pyrosequencing. We extracted DNA from rectal mucosal biopsies and measured bacterial levels by quantitative PCR of the 16S ribosomal RNA gene. Local cytokine gene expression was also determined in mucosal biopsies from adenoma cases and controls by quantitative PCR. The mean log abundance of Fusobacterium or cytokine gene expression between cases and controls was compared by t-test. Logistic regression was used to compare tertiles of Fusobacterium abundance. Adenoma subjects had a significantly higher abundance of Fusobacterium species compared to controls (p = 0.01). Compared to the lowest tertile, subjects with high abundance of Fusobacterium were significantly more likely to have adenomas (OR 3.66, 95% CI 1.37-9.74, p-trend 0.005). Cases but not controls had a significant positive correlation between local cytokine gene expression and Fusobacterium abundance. Among cases, the correlation for local TNF-α and Fusobacterium was r = 0.33, p = 0.06 while it was 0.44, p = 0.01 for Fusobacterium and IL-10. These results support a link between the abundance of Fusobacterium in colonic mucosa and adenomas and suggest a possible role for mucosal inflammation in this process.http://europepmc.org/articles/PMC3546075?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Amber N McCoy
Félix Araújo-Pérez
Andrea Azcárate-Peril
Jen Jen Yeh
Robert S Sandler
Temitope O Keku
spellingShingle Amber N McCoy
Félix Araújo-Pérez
Andrea Azcárate-Peril
Jen Jen Yeh
Robert S Sandler
Temitope O Keku
Fusobacterium is associated with colorectal adenomas.
PLoS ONE
author_facet Amber N McCoy
Félix Araújo-Pérez
Andrea Azcárate-Peril
Jen Jen Yeh
Robert S Sandler
Temitope O Keku
author_sort Amber N McCoy
title Fusobacterium is associated with colorectal adenomas.
title_short Fusobacterium is associated with colorectal adenomas.
title_full Fusobacterium is associated with colorectal adenomas.
title_fullStr Fusobacterium is associated with colorectal adenomas.
title_full_unstemmed Fusobacterium is associated with colorectal adenomas.
title_sort fusobacterium is associated with colorectal adenomas.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description The human gut microbiota is increasingly recognized as a player in colorectal cancer (CRC). While particular imbalances in the gut microbiota have been linked to colorectal adenomas and cancer, no specific bacterium has been identified as a risk factor. Recent studies have reported a high abundance of Fusobacterium in CRC subjects compared to normal subjects, but this observation has not been reported for adenomas, CRC precursors. We assessed the abundance of Fusobacterium species in the normal rectal mucosa of subjects with (n = 48) and without adenomas (n = 67). We also confirmed previous reports on Fusobacterium and CRC in 10 CRC tumor tissues and 9 matching normal tissues by pyrosequencing. We extracted DNA from rectal mucosal biopsies and measured bacterial levels by quantitative PCR of the 16S ribosomal RNA gene. Local cytokine gene expression was also determined in mucosal biopsies from adenoma cases and controls by quantitative PCR. The mean log abundance of Fusobacterium or cytokine gene expression between cases and controls was compared by t-test. Logistic regression was used to compare tertiles of Fusobacterium abundance. Adenoma subjects had a significantly higher abundance of Fusobacterium species compared to controls (p = 0.01). Compared to the lowest tertile, subjects with high abundance of Fusobacterium were significantly more likely to have adenomas (OR 3.66, 95% CI 1.37-9.74, p-trend 0.005). Cases but not controls had a significant positive correlation between local cytokine gene expression and Fusobacterium abundance. Among cases, the correlation for local TNF-α and Fusobacterium was r = 0.33, p = 0.06 while it was 0.44, p = 0.01 for Fusobacterium and IL-10. These results support a link between the abundance of Fusobacterium in colonic mucosa and adenomas and suggest a possible role for mucosal inflammation in this process.
url http://europepmc.org/articles/PMC3546075?pdf=render
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