Evidence map›Paper›PMID 42836017›Full record

ArticleFrontiers in pediatrics2026

Altered gut microbial functional landscape in children with pediatric inflammatory multisystem syndrome following SARS-CoV-2 infection: an exploratory metagenomic study.

J Agrimbau Vázquez, C Boggio Marzet, R Peralta, R Taussig, P Lopez, D Viale, C Alonso, T Curtti, M L Perez Gagni, M L Cassará and 2 more

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

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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

12 authors.

J Agrimbau Vázquez *Hospital de Pediatría "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.
C Boggio Marzet *Facultad de Medicina, Universidad de Buenos Aires Buenos Aires, Argentina.
R Peralta *Facultad de Ingeniería, Universidad Austral, Laboratorio de Investigación, Desarrollo y Transferencia de la Universidad Austral (LIDTUA-CIC), Pilar, Argentina.
R TaussigFacultad de Ingeniería, Universidad Austral, Laboratorio de Investigación, Desarrollo y Transferencia de la Universidad Austral (LIDTUA-CIC), Pilar, Argentina.
P LopezFacultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario (UNR) Rosario, Argentina.
D VialeHospital de Pediatría "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.
C AlonsoHospital de Pediatría "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.
T CurttiHospital de Pediatría "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.
M L Perez GagniHospital de Pediatría "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.
M L CassaráFundación Pablo Cassará, Buenos Aires, Argentina.
L UrrutiaHospital de Pediatría "Prof. Dr. J. P. Garrahan", Buenos Aires, Argentina.
J P BustamanteFacultad de Ingeniería, Universidad Austral, Laboratorio de Investigación, Desarrollo y Transferencia de la Universidad Austral (LIDTUA-CIC), Pilar, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pediatric Inflammatory Multisystem Syndrome (PIMS), also known as MIS-C (Multisystem inflammatory syndrome in children), is a severe post-infectious inflammatory condition associated with SARS-CoV-2 in children. While coronavirus disease 2019 (COVID-19), caused by SARS-CoV-2, primarily affects the respiratory system, growing evidence highlights gastrointestinal involvement and the relevance of the gut-lung axis in systemic inflammation. However, the taxonomic and, particularly, the functional landscape of the gut microbiome in children with PIMS remains insufficiently characterized. Methods: This exploratory study analyzed fecal samples from pediatric patients diagnosed with PIMS and age-matched clinically healthy controls using shotgun metagenomic sequencing. Taxonomic profiling was performed with MetaPhlAn4, and functional and metabolic pathway analyses were conducted using HUMAnN3. Alpha and beta diversity metrics were assessed, and differential abundance analyses were applied to identify microbial taxa and putative functional pathways associated with PIMS. Results: 12 pediatric patients diagnosed with PIMS and 11 age-matched clinically healthy controls were included. Alpha diversity indices did not differ significantly between groups, although consistently lower mean values were observed in children with PIMS. In contrast, beta diversity analysis demonstrated a significant separation in microbial community composition between patients with PIMS and controls (PERMANOVA, Conclusion: These findings suggest an association between gut microbiota unbalance, potential microbial functional alterations, and PIMS, supporting the need for further investigation of the gut microbiome in post-COVID-19 systemic inflammation in pediatric populations. Given the exploratory nature of this study, these observations require validation in larger, longitudinal cohorts before microbial biomarkers or therapeutic implications can be established.

Indexed as

COVID-19gut–lung axisgut microbiotametagenomicsMIS-Cpediatric inflammatory multisystem syndromePIMSSARS-CoV-2

Identifiers

PMID42836017
PMCPMC13636897

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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.