Enterotype-based Analysis of Gut Microbiota along the Conventional Adenoma-Carcinoma Colorectal Cancer Pathway.
Tzu-Wei YangWei-Hsiang LeeSiang-Jyun TuWei-Chih HuangHui-Mei ChenTing-Hsuan SunMing-Chang TsaiChi-Chih WangHsuan-Yi ChenChi-Chou HuangBei-Hao ShiuTzu-Ling YangHsin-Tzu HuangYu-Pao ChouChih-Hung ChouYa-Rong HuangYi-Run SunChao LiangFeng-Mao LinShinn-Ying HoWen-Liang ChenChiao-Wen LinKwo-Chang UengHsien-Da HuangChien-Ning HuangYuh-Jyh JongChun-Che LinPublished in: Scientific reports (2019)
The dysbiosis of human gut microbiota is strongly associated with the development of colorectal cancer (CRC). The dysbiotic features of the transition from advanced polyp to early-stage CRC are largely unknown. We performed a 16S rRNA gene sequencing and enterotype-based gut microbiota analysis study. In addition to Bacteroides- and Prevotella-dominated enterotypes, we identified an Escherichia-dominated enterotype. We found that the dysbiotic features of CRC were dissimilar in overall samples and especially Escherichia-dominated enterotype. Besides a higher abundance of Fusobacterium, Enterococcus, and Aeromonas in all CRC faecal microbiota, we found that the most notable characteristic of CRC faecal microbiota was a decreased abundance of potential beneficial butyrate-producing bacteria. Notably, Oscillospira was depleted in the transition from advanced adenoma to stage 0 CRC, whereas Haemophilus was depleted in the transition from stage 0 to early-stage CRC. We further identified 7 different CAGs by analysing bacterial clusters. The abundance of microbiota in cluster 3 significantly increased in the CRC group, whereas that of cluster 5 decreased. The abundance of both cluster 5 and cluster 7 decreased in the Escherichia-dominated enterotype of the CRC group. We present the first enterotype-based faecal microbiota analysis. The gut microbiota of colorectal neoplasms can be influenced by its enterotype.