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DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model

BACKGROUND: There is a significant demand for colorectal cancer (CRC) screening methods that are noninvasive, inexpensive, and capable of accurately detecting early stage tumors. It has been shown that models based on the gut microbiota can complement the fecal occult blood test and fecal immunochem...

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Autores principales: Baxter, Nielson T., Koumpouras, Charles C., Rogers, Mary A. M., Ruffin, Mack T., Schloss, Patrick D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109736/
https://www.ncbi.nlm.nih.gov/pubmed/27842559
http://dx.doi.org/10.1186/s40168-016-0205-y
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author Baxter, Nielson T.
Koumpouras, Charles C.
Rogers, Mary A. M.
Ruffin, Mack T.
Schloss, Patrick D.
author_facet Baxter, Nielson T.
Koumpouras, Charles C.
Rogers, Mary A. M.
Ruffin, Mack T.
Schloss, Patrick D.
author_sort Baxter, Nielson T.
collection PubMed
description BACKGROUND: There is a significant demand for colorectal cancer (CRC) screening methods that are noninvasive, inexpensive, and capable of accurately detecting early stage tumors. It has been shown that models based on the gut microbiota can complement the fecal occult blood test and fecal immunochemical test (FIT). However, a barrier to microbiota-based screening is the need to collect and store a patient’s stool sample. RESULTS: Using stool samples collected from 404 patients, we tested whether the residual buffer containing resuspended feces in FIT cartridges could be used in place of intact stool samples. We found that the bacterial DNA isolated from FIT cartridges largely recapitulated the community structure and membership of patients’ stool microbiota and that the abundance of bacteria associated with CRC were conserved. We also found that models for detecting CRC that were generated using bacterial abundances from FIT cartridges were equally predictive as models generated using bacterial abundances from stool. CONCLUSIONS: These findings demonstrate the potential for using residual buffer from FIT cartridges in place of stool for microbiota-based screening for CRC. This may reduce the need to collect and process separate stool samples and may facilitate combining FIT and microbiota-based biomarkers into a single test. Additionally, FIT cartridges could constitute a novel data source for studying the role of the microbiome in cancer and other diseases.
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spelling pubmed-51097362016-11-28 DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model Baxter, Nielson T. Koumpouras, Charles C. Rogers, Mary A. M. Ruffin, Mack T. Schloss, Patrick D. Microbiome Research BACKGROUND: There is a significant demand for colorectal cancer (CRC) screening methods that are noninvasive, inexpensive, and capable of accurately detecting early stage tumors. It has been shown that models based on the gut microbiota can complement the fecal occult blood test and fecal immunochemical test (FIT). However, a barrier to microbiota-based screening is the need to collect and store a patient’s stool sample. RESULTS: Using stool samples collected from 404 patients, we tested whether the residual buffer containing resuspended feces in FIT cartridges could be used in place of intact stool samples. We found that the bacterial DNA isolated from FIT cartridges largely recapitulated the community structure and membership of patients’ stool microbiota and that the abundance of bacteria associated with CRC were conserved. We also found that models for detecting CRC that were generated using bacterial abundances from FIT cartridges were equally predictive as models generated using bacterial abundances from stool. CONCLUSIONS: These findings demonstrate the potential for using residual buffer from FIT cartridges in place of stool for microbiota-based screening for CRC. This may reduce the need to collect and process separate stool samples and may facilitate combining FIT and microbiota-based biomarkers into a single test. Additionally, FIT cartridges could constitute a novel data source for studying the role of the microbiome in cancer and other diseases. BioMed Central 2016-11-14 /pmc/articles/PMC5109736/ /pubmed/27842559 http://dx.doi.org/10.1186/s40168-016-0205-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Baxter, Nielson T.
Koumpouras, Charles C.
Rogers, Mary A. M.
Ruffin, Mack T.
Schloss, Patrick D.
DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
title DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
title_full DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
title_fullStr DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
title_full_unstemmed DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
title_short DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
title_sort dna from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109736/
https://www.ncbi.nlm.nih.gov/pubmed/27842559
http://dx.doi.org/10.1186/s40168-016-0205-y
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