TY - JOUR
T1 - Two distinct metacommunities characterize the gut microbiota in Crohn's disease patients
AU - He, Qing
AU - Gao, Yuan
AU - Jie, Zhuye
AU - Yu, Xinlei
AU - Laursen, Janne Marie
AU - Xiao, Liang
AU - Li, Ying
AU - Li, Lingling
AU - Zhang, Faming
AU - Feng, Qiang
AU - Li, Xiaoping
AU - Yu, Jinghong
AU - Liu, Chuan
AU - Lan, Ping
AU - Yan, Ting
AU - Liu, Xin
AU - Xu, Xun
AU - Yang, Huanming
AU - Wang, Jian
AU - Madsen, Lise
AU - Pedersen, Susanne Brix
AU - Wang, Jianping
AU - Kristiansen, Karsten
AU - Jia, Huijue
PY - 2017
Y1 - 2017
N2 - The inflammatory intestinal disorder Crohn's disease (CD) has become a health challenge worldwide. The gut microbiota closely interacts with the host immune system, but its functional impact in CD is unclear. Except for studies on a small number of CD patients, analyses of the gut microbiota in CD have used 16S rDNA amplicon sequencing. Here we employed metagenomic shotgun sequencing to provide a detailed characterization of the compositional and functional features of the CD microbiota, comprising also unannotated bacteria, and investigated its modulation by exclusive enteral nutrition (EEN). Based on signature taxa, CD microbiotas clustered into two distinct metacommunities indicating individual variability in CD microbiome structure. Metacommunity-specific functional shifts in CD showed enrichment in producers of the pro-inflammatory hexa-acylated lipopolysaccharide variant and a reduction in the potential to synthesize short chain fatty acids. Disruption of ecological networks was evident in CD, coupled with reduction in growth rates of many bacterial species. Short-term EEN elicited limited impact on the overall composition of the CD microbiota, although functional changes occurred following treatment. The microbiotas in CD patients can be stratified into two distinct metacommunities with the most severely perturbed metacommunity exhibiting functional potentials that deviate markedly from that of the healthy individuals with possible implication in relation to CD pathogenesis.
AB - The inflammatory intestinal disorder Crohn's disease (CD) has become a health challenge worldwide. The gut microbiota closely interacts with the host immune system, but its functional impact in CD is unclear. Except for studies on a small number of CD patients, analyses of the gut microbiota in CD have used 16S rDNA amplicon sequencing. Here we employed metagenomic shotgun sequencing to provide a detailed characterization of the compositional and functional features of the CD microbiota, comprising also unannotated bacteria, and investigated its modulation by exclusive enteral nutrition (EEN). Based on signature taxa, CD microbiotas clustered into two distinct metacommunities indicating individual variability in CD microbiome structure. Metacommunity-specific functional shifts in CD showed enrichment in producers of the pro-inflammatory hexa-acylated lipopolysaccharide variant and a reduction in the potential to synthesize short chain fatty acids. Disruption of ecological networks was evident in CD, coupled with reduction in growth rates of many bacterial species. Short-term EEN elicited limited impact on the overall composition of the CD microbiota, although functional changes occurred following treatment. The microbiotas in CD patients can be stratified into two distinct metacommunities with the most severely perturbed metacommunity exhibiting functional potentials that deviate markedly from that of the healthy individuals with possible implication in relation to CD pathogenesis.
KW - Crohn's disease
KW - Exclusive enteral nutrition
KW - Gut microbe
KW - Metagenomics
U2 - 10.1093/gigascience/gix050
DO - 10.1093/gigascience/gix050
M3 - Journal article
C2 - 28655159
SN - 2047-217X
VL - 6
JO - GigaScience
JF - GigaScience
IS - 7
ER -