Preliminary Comparison of Oral and Intestinal Human Microbiota in Patients with Colorectal Cancer: A Pilot Study

• Published in: Frontiers in microbiology Vol. 8; p. 2699
• Main Authors: Russo, Edda, Bacci, Giovanni, Chiellini, Carolina, Fagorzi, Camilla, Niccolai, Elena, Taddei, Antonio, Ricci, Federica, Ringressi, Maria N, Borrelli, Rossella, Melli, Filippo, Miloeva, Manouela, Bechi, Paolo, Mengoni, Alessio, Fani, Renato, Amedei, Amedeo
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 12-01-2018
• Subjects: colorectal cancer; Fusobacterium nucleatum; gut microbiota; Microbiology; oral microbiota; quantitative polymerase chain reaction; taxonomic analysis; quantitative polymerase chain reaction; colorectal cancer; Fusobacterium nucleatum; oral microbiota; taxonomic analysis; gut microbiota
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2017.02699

In this study Next-Generation Sequencing (NGS) was used to analyze and compare human microbiota from three different compartments, i.e., saliva, feces, and cancer tissue (CT), of a selected cohort of 10 Italian patients with colorectal cancer (CRC) vs. 10 healthy controls (saliva and feces). Furthermore, the
abundance in the same body site was investigated through real-time quantitative polymerase chain reaction (qPCR) to assess the association with CRC. Differences in bacterial composition,
abundance in healthy controls vs. CRC patients, and the association of
with clinical parameters were observed. Taxonomic analysis based on 16S rRNA gene, revealed the presence of three main bacterial phyla, which includes about 80% of reads:
(39.18%),
(30.36%), and
(10.65%). The results highlighted the presence of different bacterial compositions; in particular, the fecal samples of CRC patients seemed to be enriched with
, whereas in the fecal samples of healthy controls
were one of the major phyla detected though these differences were not statistically significant. The CT samples showed the highest alpha diversity values. These results emphasize a different taxonomic composition of feces from CRC compared to healthy controls. Despite the low number of samples included in the study, these results suggest the importance of microbiota in the CRC progression and could pave the way to the development of therapeutic interventions and novel microbial-related diagnostic tools in CRC patients.