4.6 Article

Fusobacterium nucleatum and Bacteroides fragilis detection in colorectal tumours: Optimal target site and correlation with total bacterial load

Journal

PLOS ONE
Volume 17, Issue 1, Pages -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0262416

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Infiltration of certain bacterial species in the mucosa may contribute to the development of colorectal cancer (CRC). This study aimed to determine the optimal site for bacterial detection in CRC tumors. The presence of Fusobacterium nucleatum and Bacteroides fragilis was detected in tumors from 43% and 24% of patients, respectively. The optimal detection site was found to be the tumor luminal surface. F. nucleatum detection was associated with more advanced disease. The study suggests a role for F. nucleatum in CRC development and highlights the significance of tumor luminal surface for bacterial detection.
BackgroundMucosal infiltration by certain bacterial species may contribute to the development and progression of colorectal cancer (CRC). There is considerable variation in reported detection rates in human CRC samples and the extent to which bacterial infiltration varies across regions of the primary tumour is unknown. This study aimed to determine if there is an optimal site for bacterial detection within CRC tumours. MethodsPresence of target bacterial species was assessed by quantitative real-time PCR (qPCR) in 42 human CRC tumours. Abundance in primary tumour regions, normal epithelium and at metastatic sites was investigated in an expanded cohort of 51 patients. Species presence/absence was confirmed by diversity profiling in five patients. Correlation with total bacterial load and clinicopathological features was assessed. ResultsFusobacterium nucleatum and Bacteroides fragilis were detected in tumours from 43% and 24% of patients, respectively (17% positive for both species). The optimal detection site was the tumour luminal surface (TLS). Patients testing positive at the TLS frequently tested negative at other sites, including central tumour and invasive margin. F. nucleatum was detected at a higher frequency in tumour versus normal epithelium (p < 0.01) and was associated with more advanced disease (p = 0.01). Detection of both species correlated with total bacterial load. However, corroboration of qPCR results via diversity profiling suggests detection of these species may indicate a specific microbial signature. ConclusionsThis study supports a role for F. nucleatum in CRC development. Presence of F. nucleatum and B. fragilis varies across primary tumour regions, with the TLS representing the optimal site for bacterial detection.

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