Depth-dependent differences in community structure of the human colonic microbiota in health.

<h4>Objective</h4>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.<h4>Design</h4>A microbiological protected specimen...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Aonghus Lavelle, Grainne Lennon, Neil Docherty, Aine Balfe, Hugh E Mulcahy, Glen Doherty, Diarmuid O Donoghue, John M Hyland, Fergus Shanahan, Kieran Sheahan, J Calvin Coffey, Desmond C Winter, P Ronan O Connell
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/b681a9f9e0c048bb9efebfac0a437464
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
Descripción
Sumario:<h4>Objective</h4>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.<h4>Design</h4>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.<h4>Results</h4>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.<h4>Conclusion</h4>These results support the concept of a microbiota with little longitudinal variability but with some degree of segregation between luminal and mucosal communities.