Evidence map›Paper›PMID 28706260›Full record

ArticleScientific reports2017

Early intervention with Bifidobacterium lactis NCC2818 modulates the host-microbe interface independent of the sustained changes induced by the neonatal environment.

Marie C Lewis, Claire A Merrifield, Bernard Berger, Olivier Cloarec, Swantje Duncker, Annick Mercenier, Jeremy K Nicholson, Elaine Holmes, Mick Bailey

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 15 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

9 authors at 4 institutions in 2 countries.

Marie C LewisFood and Nutritional Sciences, School of Chemistry, Food and Pharmacy, University of Reading, Reading, RG6 6AP, UK. marie.lewis@reading.ac.uk.
Claire A MerrifieldBiomolecular Medicine, Department of Surgery and Cancer, Imperial College London, SW7 2AZ, London, UK.
Bernard BergerNestlé Research Centre, Vers-chez-les-Blanc, 1000, Lausanne 26, Switzerland.
Olivier CloarecKorrigan Sciences Ltd., Maidenhead, SL6 2GN, UK.
Swantje DunckerNestlé Research Centre, Vers-chez-les-Blanc, 1000, Lausanne 26, Switzerland.
Annick MercenierNestlé Research Centre, Vers-chez-les-Blanc, 1000, Lausanne 26, Switzerland.
Jeremy K NicholsonBiomolecular Medicine, Department of Surgery and Cancer, Imperial College London, SW7 2AZ, London, UK.
Elaine HolmesBiomolecular Medicine, Department of Surgery and Cancer, Imperial College London, SW7 2AZ, London, UK.
Mick BaileyInfection and Immunity, Department of Clinical Veterinary Science, University of Bristol, Langford House, Langford, North Somerset, BS40 5DU, UK.
Imperial College London · GBNestlé (Switzerland) · CHUniversity of Bristol · GBUniversity of Reading · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory and metabolic diseases can originate during early-life and have been correlated with shifts in intestinal microbial ecology. Here we demonstrate that minor environmental fluctuations during the early neonatal period had sustained effects on the developing porcine microbiota and host-microbe interface. These inter-replicate effects appear to originate during the first day of life, and are likely to reflect very early microbiota acquisition from the environment. We statistically link early systemic inflammation with later local increases in inflammatory cytokine (IL-17) production, which could have important enteric health implications. Immunity, intestinal barrier function, host metabolism and host-microbiota co-metabolism were further modified by Bifidobacterium lactis NCC2818 supplementation, although composition of the in situ microbiota remained unchanged. Finally, our robust model identified novel, strong correlations between urinary metabolites (eg malonate, phenylacetylglycine, alanine) and mucosal immunoglobulin (IgM) and cytokine (IL-10, IL-4) production, thus providing the possibility of the development of urinary 'dipstick' tests to assess non-accessible mucosal immune development and identify early precursors (biomarkers) of disease. These results have important implications for infants exposed to neonatal factors including caesarean delivery, antibiotic therapy and delayed discharge from hospital environments, which may predispose to the development of inflammatory and metabolic diseases in later life.

Indexed as

Environmental ExposureGastrointestinal MicrobiomeAnimalsAnimals, NewbornBifidobacterium animalisEarly Intervention, EducationalImmunity, MucosalMetabolic DiseasesProbioticsSwineSwine DiseasesSystemic Inflammatory Response Syndrome

Identifiers

PMID28706260
PMCPMC5509696
OpenAlexW2732702761

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.