Evidence map›Paper›PMID 26077811›Full record

ArticleProteomics2015

Metaproteomics reveals functional shifts in microbial and human proteins during a preterm infant gut colonization case.

Jacque C Young, Chongle Pan, Rachel M Adams, Brandon Brooks, Jillian F Banfield, Michael J Morowitz, Robert L Hettich

Open access · greenAbstract read
In one paragraph

Article in Proteomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
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

29 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  6. Considerations for constructing a protein sequence database for metaproteomics.Computational and structural biotechnology journal · 2022
    Review
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  8. Article
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  11. Article
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  19. The Preterm Gut Microbiota: An Inconspicuous Challenge in Nutritional Neonatal Care.Frontiers in cellular and infection microbiology · 2019
    Review
  20. 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

7 authors at 5 institutions in 1 country.

Jacque C YoungGenome Sciences and Technology Graduate School, University of Tennessee, Knoxville, TN, USA.
Chongle PanChemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
Rachel M AdamsGenome Sciences and Technology Graduate School, University of Tennessee, Knoxville, TN, USA.
Brandon BrooksDepartment of Earth and Planetary Sciences, University of California, Berkeley, CA, USA.
Jillian F BanfieldDepartment of Earth and Planetary Sciences, University of California, Berkeley, CA, USA.
Michael J MorowitzDivision of Pediatric General & Thoracic Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Robert L HettichChemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
Oak Ridge National Laboratory · USPlanetary Science Institute · USUniversity of Pennsylvania · USUniversity of Pittsburgh · USUniversity of Tennessee at Knoxville · US

Funding

Proteogenomic analysis of inflammation and dysbiosis in the infant gutR01GM103600 · NIGMS · UT-BATTELLE, LLC-OAK RIDGE NATIONAL LAB · PI BANFIELD, JILLIAN, HETTICH, ROBERT L. · 2014 to 2017
$1.5M
NIGMS NIH HHS 1R01-GM-103600NIGMS NIH HHS R01 GM103600
6 · The paper itself

Abstract

Microbial colonization of the human gastrointestinal tract plays an important role in establishing health and homeostasis. However, the time-dependent functional signatures of microbial and human proteins during early colonization of the gut have yet to be determined. To this end, we employed shotgun proteomics to simultaneously monitor microbial and human proteins in fecal samples from a preterm infant during the first month of life. Microbial community complexity increased over time, with compositional changes that were consistent with previous metagenomic and rRNA gene data. More specifically, the function of the microbial community initially involved biomass growth, protein production, and lipid metabolism, and then switched to more complex metabolic functions, such as carbohydrate metabolism, once the community stabilized and matured. Human proteins detected included those responsible for epithelial barrier function and antimicrobial activity. Some neutrophil-derived proteins increased in abundance early in the study period, suggesting activation of the innate immune system. Likewise, abundances of cytoskeletal and mucin proteins increased later in the time course, suggestive of subsequent adjustment to the increased microbial load. This study provides the first snapshot of coordinated human and microbial protein expression in a preterm infant's gut during early development.

Indexed as

MetagenomicsProteomicsFecesGastrointestinal TractHumansInfantInfant, NewbornInfant, PrematureMicrobiotaInfant gutMetaproteomicsMicrobial colonizationMicrobiomeSystems biology

Identifiers

PMID26077811
PMCPMC4607655
OpenAlexW2159243770

What OpenQuestion holds

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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.