Evidence map›Paper›PMID 30901843›Full record

ArticleInternational journal of molecular sciences2019

Metaproteomic and 16S rRNA Gene Sequencing Analysis of the Infant Fecal Microbiome.

Laetitia Cortes, Harm Wopereis, Aude Tartiere, Julie Piquenot, Joost W Gouw, Sebastian Tims, Jan Knol, Daniel Chelsky

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Microbiota, Food, and Health.International journal of molecular sciences · 2019
    Article
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

8 authors.

Laetitia CortesCaprion Biosciences, 201 President Kennedy, Suite PK-3900, Montreal, QC H2X3Y7, Canada. lcortes@caprion.com.
Harm WopereisDanone Nutricia Research, Gut Biology and Microbiology, Uppsalalaan 12, 3584 CT Utrecht, The Netherlands. harm.wopereis@wur.nl.
Aude TartiereCaprion Biosciences, 201 President Kennedy, Suite PK-3900, Montreal, QC H2X3Y7, Canada. aude.tartiere@gmail.com.
Julie PiquenotCaprion Biosciences, 201 President Kennedy, Suite PK-3900, Montreal, QC H2X3Y7, Canada. juliepiq@gmail.com.
Joost W GouwDanone Nutricia Research, Gut Biology and Microbiology, Uppsalalaan 12, 3584 CT Utrecht, The Netherlands. joost.gouw@danone.com.ORCID 0000-0002-3514-2987
Sebastian TimsDanone Nutricia Research, Gut Biology and Microbiology, Uppsalalaan 12, 3584 CT Utrecht, The Netherlands. sebastian.tims@danone.com.
Jan KnolDanone Nutricia Research, Gut Biology and Microbiology, Uppsalalaan 12, 3584 CT Utrecht, The Netherlands. jan.knol@wur.nl.
Daniel ChelskyCaprion Biosciences, 201 President Kennedy, Suite PK-3900, Montreal, QC H2X3Y7, Canada. dchelsky@caprion.com.ORCID 0000-0002-8126-2525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A metaproteomic analysis was conducted on the fecal microbiome of eight infants to characterize global protein and pathway expression. Although mass spectrometry-based proteomics is now a routine tool, analysis of the microbiome presents specific technical challenges, including the complexity and dynamic range of member taxa, the need for well-annotated metagenomic databases, and high inter-protein sequence redundancy and similarity. In this study, an approach was developed for assessment of biological phenotype and metabolic status, as a functional complement to DNA sequence analysis. Fecal samples were prepared and analysed by tandem mass spectrometry and a homology-based meta-clustering strategy was used to combine peptides from multiple species into representative proteins. In total, 15,250 unique peptides were sequenced and assigned to 2154 metaclusters, which were then assigned to pathways and functional groups. Differences were noted in several pathways, consistent with the dominant genera observed in different subjects. Although this study was not powered to draw conclusions from the comparisons, the results obtained demonstrate the applicability of this approach and provide the methods needed for performing semi-quantitative comparisons of human fecal microbiome composition, physiology and metabolism, as well as a more detailed assessment of microbial composition in comparison to 16S rRNA gene sequencing.

Indexed as

Gastrointestinal MicrobiomeMetagenomicsProteomicsRNA, Ribosomal, 16SAnti-Bacterial AgentsFecesFemaleHumansInfantInformaticsMaleMetagenomeProteomeAnti-Bacterial AgentsProteomeRNA, Ribosomal, 16Sfecalinfantsintestinalmass spectrometrymetabolismmetaclustermicrobiome

Identifiers

PMID30901843
PMCPMC6471839

What OpenQuestion holds

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LicenceCC BY
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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.