Evidence map›Paper›PMID 36707764›Full record

ArticleBMC microbiology2023

In vitro gut microbiome response to carbohydrate supplementation is acutely affected by a sudden change in diet.

Ida Gisela Pantoja-Feliciano, J Philip Karl, Matthew Perisin, Laurel A Doherty, Holly L McClung, Nicholes J Armstrong, Rebecca Renberg, Kenneth Racicot, Tobyn Branck, Steve Arcidiacono and 1 more

Abstract read
In one paragraph

Article in BMC microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Phytosynbiotic Containing Double-Layer MicroencapsulatedAnimals : an open access journal from MDPI · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
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

11 authors.

Ida Gisela Pantoja-FelicianoSoldier Effectiveness Directorate (SED), U.S. Army DEVCOM Soldier Center, Natick, MA, USA.
J Philip KarlMilitary Nutrition Division, U.S. Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
Matthew PerisinU.S. Army DEVCOM Army Research Laboratory, Adelphi, MD, USA.
Laurel A DohertySoldier Effectiveness Directorate (SED), U.S. Army DEVCOM Soldier Center, Natick, MA, USA.
Holly L McClungMilitary Nutrition Division, U.S. Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
Nicholes J ArmstrongMilitary Nutrition Division, U.S. Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
Rebecca RenbergGeneral Technical Services, U.S. Army DEVCOM Army Research Laboratory, Adelphi, MD, USA.
Kenneth RacicotSoldier Effectiveness Directorate (SED), U.S. Army DEVCOM Soldier Center, Natick, MA, USA.
Tobyn BranckSoldier Effectiveness Directorate (SED), U.S. Army DEVCOM Soldier Center, Natick, MA, USA.
Steve ArcidiaconoSoldier Effectiveness Directorate (SED), U.S. Army DEVCOM Soldier Center, Natick, MA, USA.
Jason W SoaresSoldier Effectiveness Directorate (SED), U.S. Army DEVCOM Soldier Center, Natick, MA, USA. jason.w.soares.civ@mail.mil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInteractions between diet, stress and the gut microbiome are of interest as a means to modulate health and performance. Here, in vitro fermentation was used to explore the effects of a sudden change in diet, 21 days sole sustenance on the Meal, Ready-to-Eat (MRE) U.S. military combat ration, on inter-species competition and functional potential of the human gut microbiota. Human fecal samples collected before and after MRE intervention or consuming a habitual diet (HAB) were introduced to nutrient-rich media supplemented with starch for in vitro fermentation under ascending colon conditions. 16S rRNA amplicon and Whole-metagenome sequencing (WMS) were used to measure community composition and functional potential. Specific statistical analyses were implemented to detect changes in relative abundance from taxa, genes and pathways.

resultsDifferential changes in relative abundance of 11 taxa, Dorea, Lachnospira, Bacteroides fragilis, Akkermansia muciniphila, Bifidobacterium adolescentis, Betaproteobacteria, Enterobacteriaceae, Bacteroides egerthii, Ruminococcus bromii, Prevotella, and Slackia, and nine Carbohydrate-Active Enzymes, specifically GH13_14, over the 24 h fermentation were observed as a function of the diet intervention and correlated to specific taxa of interest.

conclusionsThese findings suggest that consuming MRE for 21 days acutely effects changes in gut microbiota structure in response to carbohydrate but may induce alterations in metabolic capacity. Additionally, these findings demonstrate the potential of starch as a candidate supplemental strategy to functionally modulate specific gut commensals during stress-induced states.

Indexed as

Gastrointestinal MicrobiomeCarbohydratesDietDietary SupplementsFecesHumansRNA, Ribosomal, 16SStarchCarbohydratesRNA, Ribosomal, 16SStarchCarbohydrate-active enzymesCarbohydrate metabolismGut microbiomeGut microbiotaIn vitro fermentationMeal Ready-to-Eat (MRE)Metabolic competitionMicrobial ecologyMicrobial functional potentialNext generation sequencing

Identifiers

PMID36707764
PMCPMC9883884

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.