posted on 2014-04-08, 14:15authored byAonghus Lavelle, Grainne Lennon, Neil G. Docherty, Áine Balfe, Hugh E Mulcahy, Glen Doherty, Diarmuid O'Donoghue, John M Hyland, Fergus Shanahan, Kieran Sheahan, Calvin J. Coffey, Desmond C. Winter, Ronan P. O'Connell
Objective: The aims of this study were to develop techniques for spatial microbial assessment in humans and to establish
colonic luminal and mucosal spatial ecology, encompassing longitudinal and cross-sectional axes.
Design: A microbiological protected specimen brush was used in conjunction with a biopsy forceps to sample the colon in
nine healthy volunteers undergoing colonoscopy. Terminal Restriction Fragment Length Polymorphism analysis was used to
determine the major variables in the spatial organization of the colonic microbiota.
Results: Protected Specimen Brush sampling retrieved region-specific, uncontaminated samples that were enriched for
bacterial DNA and depleted in human DNA when compared to biopsy samples. Terminal Restriction Fragment Length
Polymorphism analysis revealed a segmentation of bacterial communities between the luminal brush and biopsy-associated
ecological niches with little variability across the longitudinal axis of the colon and reduced diversity in brush samples.
Conclusion: These results support the concept of a microbiota with little longitudinal variability but with some degree of
segregation between luminal and mucosal communities.