Metagenomics analysis of cultured mucosal bacteria from colorectal cancer and adjacent normal mucosal tissues. Issue 4 (25th April 2022)

• Record Type: Journal Article
• Authors: Zhu, Yubing; Ma, Ling; Wei, Wenting; Li, Xiang; Chang, Yuxiao; Pan, Zhiyuan; Gao, Hong; Yang, Ruifu; Bi, Yujing; Ding, Lei
• Is Part Of: Journal of medical microbiology. Volume 71:Issue 4(2022)
• Publication Date: 2022-04-25
• Subjects: metagenomics -- culture -- colorectal cancer -- mucosa tissue -- gut microbiota; Medical microbiology -- Periodicals; 616.9041
• DOI: 10.1099/jmm.0.001523
• Languages: English
• ISSNs: 0022-2615

Abstract

Abstract : Introduction. Colorectal cancer (CRC) is one of the most common cancers worldwide. Multiple risk factors are involved in CRC development, including age, genetics, lifestyle, diet and environment. Of these, the role of the gut microbiota in cancer biology is increasingly recognized. Hypothesis/Gap Statement. Micro-organisms have been widely detected in stool samples, but few mucosal samples have been detected and sequenced in depth. Aim. Analysis of cultured mucosal bacteria from colorectal cancer and adjacent normal mucosal tissues with metagenomics sequencing. Methodology. Twenty-eight paired tumour and non-tumour tissues from 14 patients undergoing surgery for CRC were analysed. We removed the influence of eukaryotic cells via culture. The composition of mucosal microbiota in intestinal mucosa were detected and analysed with metagenomic sequencing. Results. Compared with non-cultured mucosal sample, 80 % bacteria species could be detected after culture. Moreover, after culture, additional 30 % bacteria could be detected, compared with non-cultured samples. Since after culture it was difficult to estimate the original abundance of microbiome, we focused on the identification of the CRC tissue-specific species. There were 298 bacterial species, which could only be cultured and detected in CRC tissues. Myroides odoratimimus and Cellulophaga baltica could be isolated from all the tumour samples of 14 CRC patients, suggesting that these species may be related to tumour occurrence and development. Further functional analysis indicated that bacteria from CRC tissues showed more active functions, including basic metabolism, signal transduction and survival activities. Conclusion. We used a new method based on culture to implement information on prokaryotic taxa, and related functions, which samples were from colorectal tissues. This method is suitable for removing eukaryotic contamination and detecting micro-organisms from other tissues.