Mucosa-Associated Microbiota in Barrett's Esophagus, Dysplasia, and Esophageal Adenocarcinoma Differ Similarly Compared With Healthy Controls. Issue 8 (3rd August 2020)
- Record Type:
- Journal Article
- Title:
- Mucosa-Associated Microbiota in Barrett's Esophagus, Dysplasia, and Esophageal Adenocarcinoma Differ Similarly Compared With Healthy Controls. Issue 8 (3rd August 2020)
- Main Title:
- Mucosa-Associated Microbiota in Barrett's Esophagus, Dysplasia, and Esophageal Adenocarcinoma Differ Similarly Compared With Healthy Controls
- Authors:
- Peter, Shajan
Pendergraft, Amanda
VanDerPol, William
Wilcox, C. Mel
Kyanam Kabir Baig, Kondal R.
Morrow, Casey
Izard, Jacques
Mannon, Peter J. - Abstract:
- Abstract : INTRODUCTION: Alterations in the composition of the human gut microbiome and its metabolites have been linked to gut epithelial neoplasia. We hypothesized that differences in mucosa-adherent Barrett's microbiota could link to risk factors, providing risk of progression to neoplasia. Methods: Paired biopsies from both diseased and nonaffected esophagus (as well as gastric cardia and gastric juice for comparison) from patients with intestinal metaplasia (n = 10), low grade dysplasia (n = 10), high grade dysplasia (n = 10), esophageal adenocarcinoma (n = 12), and controls (n = 10) were processed for mucosa-associated bacteria and analyzed by 16S ribosomal ribonucleic acid V4 gene DNA sequencing. Taxa composition was tested using a generalized linear model based on the negative binomial distribution and the log link functions of the R Bioconductor package edgeR. Results: The microbe composition of paired samples (disease vs nondisease) comparing normal esophagus with intestinal metaplasia, low grade dysplasia, high grade dysplasia, and adenocarcinoma showed significant decreases in the phylum Planctomycetes and the archaean phylum Crenarchaeota ( P < 0.05, false discovery rate corrected) in diseased tissue compared with healthy controls and intrasample controls (gastric juice and unaffected mucosa). Genera Siphonobacter, Balneola, Nitrosopumilus, and Planctomyces were significantly decreased ( P < 0.05, false discovery rate corrected), representing <10% of the entireAbstract : INTRODUCTION: Alterations in the composition of the human gut microbiome and its metabolites have been linked to gut epithelial neoplasia. We hypothesized that differences in mucosa-adherent Barrett's microbiota could link to risk factors, providing risk of progression to neoplasia. Methods: Paired biopsies from both diseased and nonaffected esophagus (as well as gastric cardia and gastric juice for comparison) from patients with intestinal metaplasia (n = 10), low grade dysplasia (n = 10), high grade dysplasia (n = 10), esophageal adenocarcinoma (n = 12), and controls (n = 10) were processed for mucosa-associated bacteria and analyzed by 16S ribosomal ribonucleic acid V4 gene DNA sequencing. Taxa composition was tested using a generalized linear model based on the negative binomial distribution and the log link functions of the R Bioconductor package edgeR. Results: The microbe composition of paired samples (disease vs nondisease) comparing normal esophagus with intestinal metaplasia, low grade dysplasia, high grade dysplasia, and adenocarcinoma showed significant decreases in the phylum Planctomycetes and the archaean phylum Crenarchaeota ( P < 0.05, false discovery rate corrected) in diseased tissue compared with healthy controls and intrasample controls (gastric juice and unaffected mucosa). Genera Siphonobacter, Balneola, Nitrosopumilus, and Planctomyces were significantly decreased ( P < 0.05, false discovery rate corrected), representing <10% of the entire genus community. These changes were unaffected by age, tobacco use, or sex for Crenarcha. DISCUSSSION: There are similar significant changes in bacterial genera in Barrett's esophageal mucosa, dysplasia, and adenocarcinoma compared with controls and intrapatient unaffected esophagus. Further work will establish the biologic plausibility of these specific microbes' contributions to protection from or induction of esophageal epithelial dysplasia. … (more)
- Is Part Of:
- Clinical and translational gastroenterology. Volume 11:Issue 8(2020)
- Journal:
- Clinical and translational gastroenterology
- Issue:
- Volume 11:Issue 8(2020)
- Issue Display:
- Volume 11, Issue 8 (2020)
- Year:
- 2020
- Volume:
- 11
- Issue:
- 8
- Issue Sort Value:
- 2020-0011-0008-0000
- Page Start:
- e00199
- Page End:
- Publication Date:
- 2020-08-03
- Subjects:
- Stomach -- Diseases -- Periodicals
Intestines -- Diseases -- Periodicals
Gastroenterology
Gastrointestinal Diseases
Liver Diseases
Intestines -- Diseases
Stomach -- Diseases
Periodical
Periodicals
Fulltext
Internet Resources
Periodicals
Electronic journals
616.33 - Journal URLs:
- http://bibpurl.oclc.org/web/52768 ↗
http://www.nature.com/ctg ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1564/ ↗
https://journals.lww.com/ctg/pages/default.aspx ↗
http://www.nature.com/ ↗ - DOI:
- 10.14309/ctg.0000000000000199 ↗
- Languages:
- English
- ISSNs:
- 2155-384X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24065.xml