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Evaluating gut microbiota profiles from archived fecal samples
Authors:Trine B Rounge  Roger Meisal  Jan Inge Nordby  Ole Herman Ambur  Thomas de Lange  Geir Hoff
Institution:1.Department of Research,Cancer Registry of Norway,Oslo,Norway;2.Department of Microbiology and Infection Control,Akershus University Hospital,L?renskog,Norway;3.Department of Medical Biochemistry,Oslo University Hospital,Oslo,Norway;4.Department of Life Sciences and Health,OsloMet – Oslo Metropolitan University,Oslo,Norway;5.Section for Bowel Cancer Screening, Cancer Registry of Norway,Oslo,Norway;6.Department of Research and Development,Telemark Hospital,Skien,Norway;7.Institute of Clinical Medicine, University of Oslo,Oslo,Norway
Abstract:

Background

Associations between colorectal cancer and microbiota have been identified. Archived fecal samples might be valuable sample sources for investigating causality in carcinogenesis and biomarkers discovery due to the potential of performing longitudinal studies. However, the quality, quantity and stability of the gut microbiota in these fecal samples must be assessed prior to such studies. We evaluated i) cross-contamination during analysis for fecal blood and ii) evaporation in stored perforated fecal immunochemical tests (iFOBT) samples, iii) temperature stability as well as iv) comparison of the gut microbiota diversity and composition in archived, iFOBT and fresh fecal samples in order to assess feasibility of large scale microbiota studies.

Methods

The microbiota profiles were obtained by sequencing the V3-V4 region of 16S rDNA gene.

Results

The iFOBT does not introduce any cross-sample contamination detectable by qPCR. Neither could we detect evaporation during freeze-thaw cycle of perforated iFOBT samples. Our results confirm room temperature stability of the gut microbiome. Diverse microbial profiles were achieved in 100% of fresh, 81% of long-term archived and 96% of iFOBT samples. Microbial diversity and composition were comparable between fresh and iFOBT samples, however, diversity differed significantly between long-term archived, fresh and iFOBT samples.

Conclusion

Our data showed that it is feasible to exploit archived fecal sample sets originally collected for testing of fecal blood. The advantages of using these sample sets for microbial biomarker discovery and longitudinal observational studies are the availability of high-quality diagnostic and follow-up data. However, care must be taken when microbiota are profiled in long-term archived fecal samples.
Keywords:
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