Evidence map›Paper›PMID 35481924›Full record

ArticleFood & function2022

Identifying single-strain growth patterns of human gut microbes in response to preterm human milk and formula.

Melinda A Engevik, Leah K Stripe, John E Baatz, Carol L Wagner, Katherine E Chetta

Open access · greenAbstract read
In one paragraph

Article in Food & function, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  9. Profiling Antibiotic Resistance inAntibiotics (Basel, Switzerland) · 2022
    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

5 authors at 1 institution in 1 country.

Melinda A EngevikDepartment of Regenerative Medicine & Cell Biology, Medical University of South Carolina, USA.ORCID http://orcid.org/0000-0002-9742-9932
Leah K StripeDepartment of Regenerative Medicine & Cell Biology, Medical University of South Carolina, USA.
John E BaatzDepartment of Pediatrics, C.P. Darby Children's Research Institute, Medical University of South Carolina, USA. chetta@musc.edu.ORCID http://orcid.org/0000-0001-5870-1000
Carol L WagnerDepartment of Pediatrics, C.P. Darby Children's Research Institute, Medical University of South Carolina, USA. chetta@musc.edu.
Katherine E ChettaDepartment of Pediatrics, C.P. Darby Children's Research Institute, Medical University of South Carolina, USA. chetta@musc.edu.ORCID http://orcid.org/0000-0002-4669-6723
Medical University of South Carolina · US

Funding

Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DON C. ROCKEY · 2020 to 2026
$8.8M
South Carolina Clinical & Translational Research Institute (SCTR)KL2TR001452 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MCRAE-CLARK, AIMEE L · 2015 to 2024
$5.9M
Identifying the role of serotonin receptor 4 and trefoil factor 3 in intestinal wound repairK01DK123195 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ENGEVIK, MELINDA ANNE · 2020 to 2024
$612k
NCATS NIH HHS KL2 TR001452NIDDK NIH HHS K01 DK123195NIDDK NIH HHS P30 DK123704
6 · The paper itself

Abstract

The intestinal microbiota of the preterm neonate has become a major research focus, with evidence emerging that the microbiota influences both short and long-term health outcomes, in the neonatal intensive care unit and beyond. Similar to the term microbiome, the preterm gut microbiome is highly influenced by diet, specifically formula and human milk use. This study aims to analyze next-generation products including preterm formula, human milk-oligosaccharide term formula, and preterm breastmilk. We used a culture-based model to differentially compare the growth patterns of individual bacterial strains found in the human intestine. This model probed 24 strains of commensal bacteria and 8 pathobiont species which have previously been found to cause sepsis in preterm neonates. Remarkable differences between strain growth and culture pH were noted after comparing models of formulas and between human milk and formula. Both formula and human milk supported the growth of commensal bacteria; however, the formula products, but not human milk, supported the growth of several specific pathogenic strains. Computational analysis revealed potential connections between long-chain fatty acid and iron uptake from formula in pathobiont organisms. These findings indicate that there is a unique profile of growth in response to human milk and formula and shed light into how the infant gut microbiota could be influenced.

Indexed as

Gastrointestinal MicrobiomeMilk, HumanBacteriaHumansInfantInfant FormulaInfant, NewbornInfant Nutritional Physiological PhenomenaInfant, Premature

Identifiers

PMID35481924
PMCPMC9713831
OpenAlexW4225102681

What OpenQuestion holds

Textmetadata
LicenceTDM
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.