TY - JOUR
T1 - Spatial variation of the native colon microbiota in healthy adults
AU - Flynn, Kaitlin J.
AU - Ruffin, Mack T.
AU - Kim Turgeon, D.
AU - Schloss, Patrick D.
N1 - Funding Information:
P.D. Schloss reports receiving a commercial research grant from Janssen Pharmaceuticals and has received and expert testimony from Blood Hurst & O'Reardon, LLP. No potential conflicts of interest were disclosed by the other authors.
Funding Information:
We thank all the individuals who volunteered for the study. This work was supported by the Rose and Lawrence C. Page Foundation (D. K. Turgeon). We would also like to thank Brian Kleiner, Chelsea Crofoot, and Kirk Herman for their roles in study coordination, subject recruitment, sample collection, and sample processing. Thanks also to GI Fellows Drs. Amy Hosmer, Alexander Larson, and Anna Tavakkoli, who assisted Dr. Turgeon with the colonoscopies.
Publisher Copyright:
© 2018 American Association for Cancer Research.
PY - 2018/7
Y1 - 2018/7
N2 - The microbiome has been implicated in the development of colorectal cancer and inflammatory bowel diseases. The specific traits of these diseases vary along the axis of the digestive tract. Further, variation in the structure of the gut microbiota has been associated with both diseases. We profiled the microbiota of the healthy proximal and distal mucosa and lumen to better understand how bacterial populations vary along the colon. We used a twocolonoscope approach to sample proximal and distal mucosal and luminal contents from the colons of 20 healthy subjects that had not undergone any bowel preparation procedure. The biopsies and home-collected stool were subjected to 16S rRNA gene sequencing, and random forest classification models were built using taxa abundance and location to identify microbiota specific to each site. The right mucosa and lumen had the most similar community structures of the five sites we considered from each subject. The distal mucosa had higher relative abundance of Finegoldia, Murdochiella, Peptoniphilus, Porphyromonas, and Anaerococcus. The proximal mucosa had more of the genera Enterobacteriaceae, Bacteroides, and Pseudomonas. The classification model performed well when classifying mucosal samples into proximal or distal sides (AUC = 0.808). Separating proximal and distal luminal samples proved more challenging (AUC = 0.599), and specific microbiota that differentiated the two were hard to identify. By sampling the unprepped colon, we identified distinct bacterial populations native to the proximal and distal sides. Further investigation of these bacteria may elucidate if and how these groups contribute to different disease processes on their respective sides of the colon.
AB - The microbiome has been implicated in the development of colorectal cancer and inflammatory bowel diseases. The specific traits of these diseases vary along the axis of the digestive tract. Further, variation in the structure of the gut microbiota has been associated with both diseases. We profiled the microbiota of the healthy proximal and distal mucosa and lumen to better understand how bacterial populations vary along the colon. We used a twocolonoscope approach to sample proximal and distal mucosal and luminal contents from the colons of 20 healthy subjects that had not undergone any bowel preparation procedure. The biopsies and home-collected stool were subjected to 16S rRNA gene sequencing, and random forest classification models were built using taxa abundance and location to identify microbiota specific to each site. The right mucosa and lumen had the most similar community structures of the five sites we considered from each subject. The distal mucosa had higher relative abundance of Finegoldia, Murdochiella, Peptoniphilus, Porphyromonas, and Anaerococcus. The proximal mucosa had more of the genera Enterobacteriaceae, Bacteroides, and Pseudomonas. The classification model performed well when classifying mucosal samples into proximal or distal sides (AUC = 0.808). Separating proximal and distal luminal samples proved more challenging (AUC = 0.599), and specific microbiota that differentiated the two were hard to identify. By sampling the unprepped colon, we identified distinct bacterial populations native to the proximal and distal sides. Further investigation of these bacteria may elucidate if and how these groups contribute to different disease processes on their respective sides of the colon.
UR - http://www.scopus.com/inward/record.url?scp=85048295870&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85048295870&partnerID=8YFLogxK
U2 - 10.1158/1940-6207.CAPR-17-0370
DO - 10.1158/1940-6207.CAPR-17-0370
M3 - Article
C2 - 29636352
AN - SCOPUS:85048295870
SN - 1940-6207
VL - 11
SP - 393
EP - 401
JO - Cancer Prevention Research
JF - Cancer Prevention Research
IS - 7
ER -