Evidence map›Paper›PMID 30504906›Full record

ArticleNature communications2018

Birth mode is associated with earliest strain-conferred gut microbiome functions and immunostimulatory potential.

Linda Wampach, Anna Heintz-Buschart, Joëlle V Fritz, Javier Ramiro-Garcia, Janine Habier, Malte Herold, Shaman Narayanasamy, Anne Kaysen, Angela H Hogan, Lutz Bindl and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed, 5 pooled it
13.3field-weighted citation impact, top 1% 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

183 citing papers in PubMed, 5 syntheses or guidelines pooled it, 287 citations in OpenAlex.

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123 more citing papers are in PubMed but not listed here.

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

17 authors at 6 institutions in 4 countries.

Linda WampachLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Anna Heintz-BuschartLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.ORCID http://orcid.org/0000-0002-9780-1933
Joëlle V FritzLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Javier Ramiro-GarciaLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Janine HabierLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Malte HeroldLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Shaman NarayanasamyLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Anne KaysenLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.
Angela H HoganIntegrated BioBank of Luxembourg, rue Louis Rech 1, 3555, Dudelange, Luxembourg.
Lutz BindlCentre Hospitalier de Luxembourg, rue Nicolas Ernest Barblé 4, 1210, Luxembourg, Luxembourg.ORCID http://orcid.org/0000-0003-1764-434X
Jean BottuCentre Hospitalier de Luxembourg, rue Nicolas Ernest Barblé 4, 1210, Luxembourg, Luxembourg.
Rashi HalderLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.ORCID http://orcid.org/0000-0002-1402-1254
Conny SjöqvistKTH Royal Institute of Technology, Science for Life Laboratory, School of Biotechnology, Division of Gene Technology, Tomtebodavägen 23a, 17165, Solna, Sweden.
Patrick MayLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg.ORCID http://orcid.org/0000-0001-8698-3770
Anders F AnderssonKTH Royal Institute of Technology, Science for Life Laboratory, School of Biotechnology, Division of Gene Technology, Tomtebodavägen 23a, 17165, Solna, Sweden.ORCID http://orcid.org/0000-0002-3627-6899
Carine de BeaufortCentre Hospitalier de Luxembourg, rue Nicolas Ernest Barblé 4, 1210, Luxembourg, Luxembourg.
Paul WilmesLuxembourg Centre for Systems Biomedicine, University of Luxembourg, avenue des Hauts-Fourneaux 7, 4362, Esch-sur-Alzette, Luxembourg. paul.wilmes@uni.lu.
University of Luxembourg · LUCentre Hospitalier de Luxembourg · LUÅbo Akademi University · FICentral Bank of Luxembourg · LUHelmholtz Centre for Environmental Research · DEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rate of caesarean section delivery (CSD) is increasing worldwide. It remains unclear whether disruption of mother-to-neonate transmission of microbiota through CSD occurs and whether it affects human physiology. Here we perform metagenomic analysis of earliest gut microbial community structures and functions. We identify differences in encoded functions between microbiomes of vaginally delivered (VD) and CSD neonates. Several functional pathways are over-represented in VD neonates, including lipopolysaccharide (LPS) biosynthesis. We link these enriched functions to individual-specific strains, which are transmitted from mothers to neonates in case of VD. The stimulation of primary human immune cells with LPS isolated from early stool samples of VD neonates results in higher levels of tumour necrosis factor (TNF-α) and interleukin 18 (IL-18). Accordingly, the observed levels of TNF-α and IL-18 in neonatal blood plasma are higher after VD. Taken together, our results support that CSD disrupts mother-to-neonate transmission of specific microbial strains, linked functional repertoires and immune-stimulatory potential during a critical window for neonatal immune system priming.

Indexed as

Cesarean SectionDelivery, ObstetricFemaleGastrointestinal MicrobiomeHumansInfant, NewbornInfectious Disease Transmission, VerticalInterleukin-18In Vitro TechniquesLipopolysaccharidesMetagenomicsPregnancyTumor Necrosis Factor-alphaIL18 protein, humanInterleukin-18LipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID30504906
PMCPMC6269548
OpenAlexW2902904448

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.