TY - JOUR
T1 - High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia
AU - Drewes, Julia L.
AU - White, James R.
AU - Dejea, Christine M.
AU - Fathi, Payam
AU - Iyadorai, Thevambiga
AU - Vadivelu, Jamuna
AU - Roslani, April C.
AU - Wick, Elizabeth C.
AU - Mongodin, Emmanuel F.
AU - Loke, Mun Fai
AU - Thulasi, Kumar
AU - Gan, Han Ming
AU - Goh, Khean Lee
AU - Chong, Hoong Yin
AU - Kumar, Sandip
AU - Wanyiri, Jane W.
AU - Sears, Cynthia L.
N1 - Funding Information:
This work was supported by the National Institutes of Health through Grants R01 CA151393 (to CLS), P30 DK089502 (GI Core), P30 CA006973 (Sidney Kimmel Comprehensive Cancer Center core), P50 CA062924 (SPORE in Gastrointestinal Cancers), JHU Institute for Cancer Immunotherapy, JHU SOM Department of Medicine, JHU SOM Department of Surgery, the Cancer Research Institute/Fight Colorectal Cancer, Swami Institute for International Medical Education (SIIME) Award (to CLS and ECW), University of Malaya Research Grant RP016A-13HTM (to JV), and an NIH Shared Instrumentation Grant S10OD016374 for the Zeiss 780 LSM confocal in the JHU Microscope Facility.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Colorectal cancer (CRC) remains the third most common cancer worldwide, with a growing incidence among young adults. Multiple studies have presented associations between the gut microbiome and CRC, suggesting a link with cancer risk. Although CRC microbiome studies continue to profile larger patient cohorts with increasingly economical and rapid DNA sequencing platforms, few common associations with CRC have been identified, in part due to limitations in taxonomic resolution and differences in analysis methodologies. Complementing these taxonomic studies is the newly recognized phenomenon that bacterial organization into biofilm structures in the mucus layer of the gut is a consistent feature of right-sided (proximal), but not left-sided (distal) colorectal cancer. In the present study, we performed 16S rRNA gene amplicon sequencing and biofilm quantification in a new cohort of patients from Malaysia, followed by a meta-analysis of eleven additional publicly available data sets on stool and tissue-based CRC microbiota using Resphera Insight, a high-resolution analytical tool for species-level characterization. Results from the Malaysian cohort and the expanded meta-analysis confirm that CRC tissues are enriched for invasive biofilms (particularly on right-sided tumors), a symbiont with capacity for tumorigenesis (Bacteroides fragilis), and oral pathogens including Fusobacterium nucleatum, Parvimonas micra, and Peptostreptococcus stomatis. Considered in aggregate, species from the Human Oral Microbiome Database are highly enriched in CRC. Although no detected microbial feature was universally present, their substantial overlap and combined prevalence supports a role for the gut microbiota in a significant percentage (>80%) of CRC cases.
AB - Colorectal cancer (CRC) remains the third most common cancer worldwide, with a growing incidence among young adults. Multiple studies have presented associations between the gut microbiome and CRC, suggesting a link with cancer risk. Although CRC microbiome studies continue to profile larger patient cohorts with increasingly economical and rapid DNA sequencing platforms, few common associations with CRC have been identified, in part due to limitations in taxonomic resolution and differences in analysis methodologies. Complementing these taxonomic studies is the newly recognized phenomenon that bacterial organization into biofilm structures in the mucus layer of the gut is a consistent feature of right-sided (proximal), but not left-sided (distal) colorectal cancer. In the present study, we performed 16S rRNA gene amplicon sequencing and biofilm quantification in a new cohort of patients from Malaysia, followed by a meta-analysis of eleven additional publicly available data sets on stool and tissue-based CRC microbiota using Resphera Insight, a high-resolution analytical tool for species-level characterization. Results from the Malaysian cohort and the expanded meta-analysis confirm that CRC tissues are enriched for invasive biofilms (particularly on right-sided tumors), a symbiont with capacity for tumorigenesis (Bacteroides fragilis), and oral pathogens including Fusobacterium nucleatum, Parvimonas micra, and Peptostreptococcus stomatis. Considered in aggregate, species from the Human Oral Microbiome Database are highly enriched in CRC. Although no detected microbial feature was universally present, their substantial overlap and combined prevalence supports a role for the gut microbiota in a significant percentage (>80%) of CRC cases.
UR - http://www.scopus.com/inward/record.url?scp=85042190738&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85042190738&partnerID=8YFLogxK
U2 - 10.1038/s41522-017-0040-3
DO - 10.1038/s41522-017-0040-3
M3 - Article
C2 - 29214046
AN - SCOPUS:85042190738
SN - 2055-5008
VL - 3
JO - npj Biofilms and Microbiomes
JF - npj Biofilms and Microbiomes
IS - 1
M1 - 34
ER -