Evidence map›Paper›PMID 33452029›Full record

ArticleApplied and environmental microbiology2021

Fecal Microbiota Nutrient Utilization Potential Suggests Mucins as Drivers for Initial Gut Colonization of Mother-Child-Shared Bacteria.

Morten Nilsen, Asima Lokmic, Inga Leena Angell, Karin C Lødrup Carlsen, Kai-Håkon Carlsen, Guttorm Haugen, Gunilla Hedlin, Christine Monceyron Jonassen, Benjamin J Marsland, Björn Nordlund and 8 more

Open access · greenAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

18 authors at 5 institutions in 3 countries.

Morten NilsenFaculty of Chemistry, Biotechnology, and Food Science, Norwegian University of Life Sciences, Ås, Norway.ORCID 0000-0002-9498-1262
Asima LokmicFaculty of Chemistry, Biotechnology, and Food Science, Norwegian University of Life Sciences, Ås, Norway.
Inga Leena AngellFaculty of Chemistry, Biotechnology, and Food Science, Norwegian University of Life Sciences, Ås, Norway.
Karin C Lødrup CarlsenDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Kai-Håkon CarlsenDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Guttorm HaugenUniversity of Oslo, Faculty of Medicine, Institute of Clinical Medicine, Oslo, Norway.
Gunilla HedlinAstrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Christine Monceyron JonassenFaculty of Chemistry, Biotechnology, and Food Science, Norwegian University of Life Sciences, Ås, Norway.
Benjamin J MarslandDepartment of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
Björn NordlundAstrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Eva Maria RehbinderDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Carina Madelen SaundersDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Håvard O SkjervenDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Lars SnipenFaculty of Chemistry, Biotechnology, and Food Science, Norwegian University of Life Sciences, Ås, Norway.
Anne Cathrine StaffUniversity of Oslo, Faculty of Medicine, Institute of Clinical Medicine, Oslo, Norway.
Cilla SöderhällAstrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Riyas VettukattilDivision of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Knut RudiFaculty of Chemistry, Biotechnology, and Food Science, Norwegian University of Life Sciences, Ås, Norway knut.rudi@nmbu.no.ORCID 0000-0002-7809-3943
Oslo University Hospital · NONorwegian University of Life Sciences · NOKarolinska University Hospital · SEMonash University · AUØstfold Hospital Trust · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nutritional drivers for mother-child sharing of bacteria and the corresponding longitudinal trajectory of the infant gut microbiota development are not yet completely settled. We therefore aimed to characterize the mother-child sharing and the inferred nutritional utilization potential for the gut microbiota from a large unselected cohort. We analyzed in depth gut microbiota in 100 mother-child pairs enrolled antenatally from the general population-based Preventing Atopic Dermatitis and Allergies in Children (PreventADALL) cohort. Fecal samples collected at gestational week 18 for mothers and at birth (meconium), 3, 6, and 12 months for infants were analyzed by reduced metagenome sequencing to determine metagenome size and taxonomic composition. The nutrient utilization potential was determined based on the Virtual Metabolic Human (VMH, www.vmh.life) database. The estimated median metagenome size was ∼150 million base pairs (bp) for mothers and ∼20 million bp at birth for the children. Longitudinal analyses revealed mother-child sharing (

Indexed as

Gastrointestinal MicrobiomeMother-Child RelationsMucinsBacteriaDelivery, ObstetricFecesFemaleHumansInfantInfant, NewbornMetagenomeMothersNutrientsMucinsNutrientsinfant gut microbiota

Identifiers

PMID33452029
PMCPMC8105027
OpenAlexW3125135424

What OpenQuestion holds

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Registered trials

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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.