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Molecular characterization of mucosal adherent bacteria and associations with colorectal adenomas.

Publication ,  Journal Article
Shen, XJ; Rawls, JF; Randall, T; Burcal, L; Mpande, CN; Jenkins, N; Jovov, B; Abdo, Z; Sandler, RS; Keku, TO
Published in: Gut Microbes
2010

The human large bowel is colonized by complex and diverse bacterial communities. However, the relationship between commensal bowel bacteria and adenomas (colorectal cancer precursors) is unclear. This study aimed to characterize adherent bacteria in normal colon and evaluate differences in community composition associated with colorectal adenomas. We evaluated adherent bacteria in normal colonic mucosa of 21 adenoma and 23 non-adenoma subjects enrolled in a cross sectional study. Terminal restriction fragment length polymorphism, clone sequencing and fluorescent in-situ hybridization analysis of the 16S rRNA genes were used to characterize adherent bacteria. A total of 335 clones were sequenced and processed for phylogenetic and taxonomic analysis. Differences in bacterial composition between cases and controls were evaluated by UniFrac and analysis of similarity matrix. Overall, Firmicutes (62%), Bacteroidetes (26%) and Proteobacteria (11%) were the most dominant phyla. The bacterial composition differed significantly between cases and controls (UniFrac p < 0.001). We observed significantly higher abundance of Proteobacteria (p < 0.05) and lower abundance of Bacteroidetes (p < 0.05) in cases compared to controls. At the genus level, case subjects showed increased abundance of Dorea spp. (p < 0.005), Faecalibacterium spp. (p < 0.05) and lower proportions of Bacteroides spp. (p < 0.03) and Coprococcus spp. (p < 0.05) than controls. Cases had higher bacterial diversity and richness than controls. These findings reveal that alterations in bacterial community composition associated with adenomas may contribute to the etiology of colorectal cancer. Extension of these findings could lead to strategies to manipulate the microbiota to prevent colorectal adenomas and cancer as well as to identify individuals at high risk.

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Published In

Gut Microbes

DOI

EISSN

1949-0984

Publication Date

2010

Volume

1

Issue

3

Start / End Page

138 / 147

Location

United States

Related Subject Headings

  • RNA, Ribosomal, 16S
  • Phylogeny
  • Molecular Sequence Data
  • Middle Aged
  • Male
  • Intestinal Mucosa
  • Humans
  • DNA, Bacterial
  • Cross-Sectional Studies
  • Colorectal Neoplasms
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Shen, X. J., Rawls, J. F., Randall, T., Burcal, L., Mpande, C. N., Jenkins, N., … Keku, T. O. (2010). Molecular characterization of mucosal adherent bacteria and associations with colorectal adenomas. Gut Microbes, 1(3), 138–147. https://doi.org/10.4161/gmic.1.3.12360
Shen, Xiang Jun, John F. Rawls, Thomas Randall, Lauren Burcal, Caroline N. Mpande, Natascha Jenkins, Biljana Jovov, Zaid Abdo, Robert S. Sandler, and Temitope O. Keku. “Molecular characterization of mucosal adherent bacteria and associations with colorectal adenomas.Gut Microbes 1, no. 3 (2010): 138–47. https://doi.org/10.4161/gmic.1.3.12360.
Shen XJ, Rawls JF, Randall T, Burcal L, Mpande CN, Jenkins N, et al. Molecular characterization of mucosal adherent bacteria and associations with colorectal adenomas. Gut Microbes. 2010;1(3):138–47.
Shen, Xiang Jun, et al. “Molecular characterization of mucosal adherent bacteria and associations with colorectal adenomas.Gut Microbes, vol. 1, no. 3, 2010, pp. 138–47. Pubmed, doi:10.4161/gmic.1.3.12360.
Shen XJ, Rawls JF, Randall T, Burcal L, Mpande CN, Jenkins N, Jovov B, Abdo Z, Sandler RS, Keku TO. Molecular characterization of mucosal adherent bacteria and associations with colorectal adenomas. Gut Microbes. 2010;1(3):138–147.

Published In

Gut Microbes

DOI

EISSN

1949-0984

Publication Date

2010

Volume

1

Issue

3

Start / End Page

138 / 147

Location

United States

Related Subject Headings

  • RNA, Ribosomal, 16S
  • Phylogeny
  • Molecular Sequence Data
  • Middle Aged
  • Male
  • Intestinal Mucosa
  • Humans
  • DNA, Bacterial
  • Cross-Sectional Studies
  • Colorectal Neoplasms