On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples

Abstract The gut microbiota plays an important role in human health and disease. Stool, rectal swab and rectal mucosal tissue samples have been used in individual studies to survey the microbial community but the consequences of using these different sample types are not completely understood. In th...

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Autores principales: Shan Sun, Xiangzhu Zhu, Xiang Huang, Harvey J. Murff, Reid M. Ness, Douglas L. Seidner, Alicia A. Sorgen, Ivory C. Blakley, Chang Yu, Qi Dai, M. Andrea Azcarate-Peril, Martha J. Shrubsole, Anthony A. Fodor
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:13d61f92d21f4c489d52b87400cedf982021-12-02T17:03:50ZOn the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples10.1038/s41598-021-94205-52045-2322https://doaj.org/article/13d61f92d21f4c489d52b87400cedf982021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-94205-5https://doaj.org/toc/2045-2322Abstract The gut microbiota plays an important role in human health and disease. Stool, rectal swab and rectal mucosal tissue samples have been used in individual studies to survey the microbial community but the consequences of using these different sample types are not completely understood. In this study, we report differences in stool, rectal swab and rectal mucosal tissue microbial communities with shotgun metagenome sequencing of 1397 stool, swab and mucosal tissue samples from 240 participants. The taxonomic composition of stool and swab samples was distinct, but less different to each other than mucosal tissue samples. Functional profile differences between stool and swab samples are smaller, but mucosal tissue samples remained distinct from the other two types. When the taxonomic and functional profiles were used for inference in association with host phenotypes of age, sex, body mass index (BMI), antibiotics or non-steroidal anti-inflammatory drugs (NSAIDs) use, hypothesis testing using either stool or rectal swab gave broadly significantly correlated results, but inference performed on mucosal tissue samples gave results that were generally less consistent with either stool or swab. Our study represents an important resource for determination of how inference can change for taxa and pathways depending on the choice of where to sample within the human gut.Shan SunXiangzhu ZhuXiang HuangHarvey J. MurffReid M. NessDouglas L. SeidnerAlicia A. SorgenIvory C. BlakleyChang YuQi DaiM. Andrea Azcarate-PerilMartha J. ShrubsoleAnthony A. FodorNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Shan Sun
Xiangzhu Zhu
Xiang Huang
Harvey J. Murff
Reid M. Ness
Douglas L. Seidner
Alicia A. Sorgen
Ivory C. Blakley
Chang Yu
Qi Dai
M. Andrea Azcarate-Peril
Martha J. Shrubsole
Anthony A. Fodor
On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
description Abstract The gut microbiota plays an important role in human health and disease. Stool, rectal swab and rectal mucosal tissue samples have been used in individual studies to survey the microbial community but the consequences of using these different sample types are not completely understood. In this study, we report differences in stool, rectal swab and rectal mucosal tissue microbial communities with shotgun metagenome sequencing of 1397 stool, swab and mucosal tissue samples from 240 participants. The taxonomic composition of stool and swab samples was distinct, but less different to each other than mucosal tissue samples. Functional profile differences between stool and swab samples are smaller, but mucosal tissue samples remained distinct from the other two types. When the taxonomic and functional profiles were used for inference in association with host phenotypes of age, sex, body mass index (BMI), antibiotics or non-steroidal anti-inflammatory drugs (NSAIDs) use, hypothesis testing using either stool or rectal swab gave broadly significantly correlated results, but inference performed on mucosal tissue samples gave results that were generally less consistent with either stool or swab. Our study represents an important resource for determination of how inference can change for taxa and pathways depending on the choice of where to sample within the human gut.
format article
author Shan Sun
Xiangzhu Zhu
Xiang Huang
Harvey J. Murff
Reid M. Ness
Douglas L. Seidner
Alicia A. Sorgen
Ivory C. Blakley
Chang Yu
Qi Dai
M. Andrea Azcarate-Peril
Martha J. Shrubsole
Anthony A. Fodor
author_facet Shan Sun
Xiangzhu Zhu
Xiang Huang
Harvey J. Murff
Reid M. Ness
Douglas L. Seidner
Alicia A. Sorgen
Ivory C. Blakley
Chang Yu
Qi Dai
M. Andrea Azcarate-Peril
Martha J. Shrubsole
Anthony A. Fodor
author_sort Shan Sun
title On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
title_short On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
title_full On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
title_fullStr On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
title_full_unstemmed On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
title_sort on the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/13d61f92d21f4c489d52b87400cedf98
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