Evidence map›Paper›PMID 34523982›Full record

ArticlemSphere2021

Comparison of Fecal Collection Methods on Variation in Gut Metagenomics and Untargeted Metabolomics.

Huihui Guan, Yanni Pu, Chenglin Liu, Tao Lou, Shishang Tan, Mengmeng Kong, Zhonghan Sun, Zhendong Mei, Qibin Qi, Zhexue Quan and 2 more

Abstract readComparative Study
In one paragraph

Article in mSphere, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  17. Omnigene-GutAMB Express · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Huihui Guan *Human Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Yanni Pu *Human Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Chenglin Liu *Human Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Tao LouHuman Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Shishang TanHuman Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Mengmeng KongHuman Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Zhonghan SunHuman Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Zhendong MeiHuman Phenome Institute, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.
Qibin QiDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, USA.
Zhexue QuanMinistry of Education Key Laboratory for Biodiversity Science and Ecological Engineering, Institute of Biodiversity Science, School of Life Sciences, Fudan Universitygrid.8547.e, Shanghai, China.ORCID 0000-0002-7561-8572
Guoping ZhaoInstitute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciencesgrid.419092.7, Chinese Academy of Sciences, Shanghai, China.
Yan ZhengState Key Laboratory of Genetic Engineering School of Life Sciences, Human Phenome Institute, Fudan Universitygrid.8547.e, Shanghai, China.ORCID 0000-0003-1129-3147

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrative analysis of high-quality metagenomics and metabolomics data from fecal samples provides novel clues for the mechanism underpinning gut microbe-human interactions. However, data regarding the influence of fecal collection methods on both metagenomics and metabolomics are sparse. Six fecal collection methods (the gold standard [GS] [i.e., immediate freezing at -80°C with no solution], 95% ethanol, RNAlater, OMNIgene Gut, fecal occult blood test [FOBT] cards, and Microlution) were used to collect 88 fecal samples from eight healthy volunteers for whole-genome shotgun sequencing (WGSS) and untargeted metabolomic profiling. Metrics assessed included the abundances of predominant phyla and α- and β-diversity at the species, gene, and pathway levels. Intraclass correlation coefficients (ICCs) were calculated for microbes and metabolites to estimate (i) stability (day 4 versus day 0 within each method), (ii) concordance (day 0 for each method versus the GS), and (iii) reliability (day 4 for each method versus the GS). For the top 4 phyla and microbial diversity metrics at the species, gene, and pathway levels, generally high stability and reliability were observed for most methods except for 95% ethanol; similar concordances were seen for different methods. For metabolomics data, 95% ethanol showed the highest stability, concordance, and reliability (median ICCs = 0.71, 0.71, and 0.65, respectively). Taken together, OMNIgene Gut, FOBT cards, RNAlater, and Microlution, but not 95% ethanol, were reliable collection methods for gut metagenomic studies. However, 95% ethanol was the best for preserving fecal metabolite profiles. We recommend using separate collecting methods for gut metagenomic sequencing and fecal metabolomic profiling in large population studies.

Indexed as

AdultDNA, BacterialEthanolFecesFemaleFreezingGastrointestinal MicrobiomeHealthy VolunteersHumansMaleMetabolomicsMetagenomeMetagenomicsReproducibility of ResultsRNA, Ribosomal, 16SSpecimen HandlingDNA, BacterialEthanolRNA, Ribosomal, 16Scollection methodfecesmetabolomicsmetagenomicsreliabilitywhole-genome shotgun sequencing

Identifiers

PMID34523982
PMCPMC8550109

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.