Evidence mapPaperPMID 41514270Full record

ArticleJournal of translational medicine2026

Unveiling balanced prenatal microbial colonization in amniotic fluid through an integrated culture and sequencing approach.

M González-Rovira, J A Sainz-Bueno, L García-Díaz, C Martínez-Pancorbo, J Sánchez, G Gutiérrez, K Magoutas, A Mesías-Pérez, E Mellado, M Payne and 2 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

M González-RoviraDepartment of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain.
J A Sainz-BuenoDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Seville, Seville, Spain.
L García-DíazDepartment of Materno-Fetal Medicine, Genetics, and Reproduction, Institute of Biomedicine of Seville (IBIS), Hospital Universitario Virgen del Rocio, CSIC/University of Seville, Seville, Spain.
C Martínez-PancorboObstetrics and Gynecology Department, Sagrado Corazón Hospital, Seville, Spain.
J SánchezDepartment of Materno-Fetal Medicine, Genetics, and Reproduction, Institute of Biomedicine of Seville (IBIS), Hospital Universitario Virgen del Rocio, CSIC/University of Seville, Seville, Spain.
G GutiérrezDepartment of Genetics, Faculty of Biology, University of Seville, Seville, Spain.
K MagoutasDivision of Obstetrics and Gynaecology, Medical School, University of Western Australia, Perth, WA, Australia.
A Mesías-PérezDepartment of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain.
E MelladoDepartment of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain.
M PayneDivision of Obstetrics and Gynaecology, Medical School, University of Western Australia, Perth, WA, Australia.
C SousaDepartment of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain.
M L MorenoDepartment of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain. lmoreno@us.es.ORCID http://orcid.org/0000-0002-7490-2037

Funding

Federación de Asociaciones de Celíacos de España (FACE) SUBN/2019/005FEDER ANDALUCIA US-15332/I+D+IMinisterio de Ciencia, Innovación y Universidades PID2024-157768OB-I00
6 · The paper itself

Abstract

backgroundThe evidence of a low-biomass microbial community in the amniotic fluid (AF) is challenging the traditional concept of a sterile womb. To clarify microbial presence and host responses, a comprehensive, multi-methodological approach is required.

methodsWe designed an optimized culturing strategy that maximized microorganism recovery by implementing differential centrifugation and concentration of AF samples, followed by plating onto four distinct selective media types and incubation under both stringent aerobic (up to two weeks) and prolonged anaerobic (up to four weeks) conditions, including an initial pre-enrichment step in Brain Heart Infusion (BHI) broth for low-abundance organisms. These results were combined with PacBio 16S rRNA gene sequencing, Illumina shotgun metagenomics, and antimicrobial peptides (AMP) detection. Using this approach, we characterized microbial presence in 154 AF samples across gestational stages. Data normality was assessed with the Shapiro-Wilk test, guiding the selection of both parametric and non-parametric tests, and a p-value of < 0.05 was considered statistically significant.

resultsWe detected culturable microorganisms in 33.1% of samples, with a higher proportion in elective caesarean Sect. (55.0%) compared to amniocentesis (29.5%), suggesting increased microbial load toward term. We applied stringent contamination controls, and repeatedly recovered viable microorganisms Bacillus, Cutibacterium, Micrococcus, and Staphylococcus, with Cutibacterium acnes and Staphylococcus epidermidis common. Both sequencing methods revealed a low-biomass, low-diversity microbial community with high inter-individual variability. Notably, striking microbial discordance in diamniotic twin pregnancies, challenged intrauterine homogeneity. Higher Human Beta Defensin (HBD) -1 levels correlated with absence of culturable bacteria or microbial DNA, while levels of HBD-1, HBD-3, and LL-37 were reduced in Staphylococcus-positive samples, suggesting a dynamic interplay between specific bacteria and host defences.

conclusionsOur findings indicate that viable bacteria and/or DNA can transiently access the prenatal environment microbial balance. We propose a novel perspective of a potential regulatory axis between microorganisms and AMP.

Indexed as

Amniotic FluidBacteriaSequence Analysis, DNAAntimicrobial PeptidesFemaleHumansMicrobiotaPregnancyRNA, Ribosomal, 16SAntimicrobial PeptidesRNA, Ribosomal, 16SAmniotic fluidBacterial cultureIllumina shotgun sequencingIntrauterine colonizationPacBio 16S rRNA gene sequencingPrenatal exposome

Identifiers

PMID41514270
PMCPMC12918369

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.