Evidence map›Paper›PMID 41350579›Full record

ArticleNPJ biofilms and microbiomes2025

Compiling an early life human gut microbiome atlas and identification of key microbial drivers.

Chiara Tarracchini, Giulia Longhi, Emma Gennaioli, Aryanna Muscò, Sonia Mirjam Rizzo, Alice Viappiani, Salvatore Giovanni Vitale, Leonardo Mancabelli, Gabriele Andrea Lugli, Stefano Angioni and 4 more

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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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

14 authors.

Chiara TarracchiniLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Giulia LonghiLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Emma GennaioliLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Aryanna MuscòLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Sonia Mirjam RizzoLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Alice ViappianiGenProbio srl, Parma, Italy.
Salvatore Giovanni VitaleDivision of Gynecology and Obstetrics, Department of Surgical Sciences, University of Cagliari, Cagliari, Italy.
Leonardo MancabelliDept. Medicine and Surgery, University of Parma, Parma, Italy.
Gabriele Andrea LugliLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Stefano AngioniDivision of Gynecology and Obstetrics, Department of Surgical Sciences, University of Cagliari, Cagliari, Italy.
Francesca TurroniLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Douwe van SinderenAPC Microbiome Institute and School of Microbiology, Bioscience Institute, National University of Ireland, Cork, Ireland.
Christian MilaniLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Marco VenturaLaboratory of Probiogenomics, Dept. Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy. marco.ventura@unipr.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the first year after birth, the infant gut microbiome undergoes a rapid and profound compositional and functional transformation, impelled by an intricate network of intrinsic and extrinsic factors. This process results in increased taxonomic and functional diversification, alongside greater interindividual variability. To better understand this early-life ecosystem, this study assessed the interindividual variability of the infant gut microbiome using a comprehensive infant gut microbiome database of 5288 fecal metagenomic data from healthy, full-term infants across various geographical locations. Our study identified six reference microbial communities, termed Early-Life Community State Types (ELi-CSTs), which not only capture specific compositional profiles and heterogeneity of the infant gut microbiome, but also record the extensive transformation experienced by this developing microbial community during the first year of human life. Indicative Species analysis and Random Forest modeling assisted the precise identification of unique, key taxonomic signatures that are critical to the structure of each ELi-CST, highlighting microbial taxa with pivotal roles in shaping the infant gut microbiota. To complement these findings, we established a bacterial biobank through dedicated cultivation efforts of the infant microbiota, comprising 182 genome-sequenced isolates corresponding to key taxa involved in early life gut microbiota assembly. This biobank provided the basis for co-cultivation experiments combined with transcriptome analyses, thereby enabling in vitro investigations into microbial cross-talk among key modulators, and yielding novel insights into the molecular interactions and cooperative dynamics behind early microbiome development.

Indexed as

BacteriaGastrointestinal MicrobiomeFecesHumansInfantInfant, NewbornMetagenomeMetagenomicsPhylogenyRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID41350579
PMCPMC12769767

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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.