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

**Authors:** 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, C. Sousa, M. L. Moreno

PMC · DOI: 10.1186/s12967-025-07601-0 · Journal of Translational Medicine · 2026-01-09

## TL;DR

This study shows that amniotic fluid contains a small but detectable microbial community, challenging the idea of a completely sterile womb during pregnancy.

## Contribution

The study introduces an integrated culture and sequencing approach to reveal transient microbial colonization and its interaction with host defenses in amniotic fluid.

## Key findings

- Culturable microorganisms were detected in 33.1% of amniotic fluid samples, with higher prevalence in caesarean samples.
- Sequencing revealed low-biomass, low-diversity microbial communities with high variability between individuals.
- Microbial presence correlated with reduced levels of certain antimicrobial peptides, suggesting a dynamic host-microbe interaction.

## Abstract

The 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.

We 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.

We 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.

Our 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.

The online version contains supplementary material available at 10.1186/s12967-025-07601-0.

## Linked entities

- **Proteins:** DEFB1 (defensin beta 1), DEFB103B (defensin beta 103B), CAMP (cathelicidin antimicrobial peptide)
- **Species:** Bacillus (taxon 1386), Cutibacterium (taxon 1912216), Micrococcus (taxon 1269), Staphylococcus (taxon 1279), Cutibacterium acnes (taxon 1747), Staphylococcus epidermidis (taxon 1282)

## Full-text entities

- **Genes:** DEFB1 (defensin beta 1) [NCBI Gene 1672] {aka BD1, DEFB-1, DEFB101, HBD1}, CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}, DEFB4A (defensin beta 4A) [NCBI Gene 1673] {aka BD-2, DEFB-2, DEFB102, DEFB2, DEFB4, HBD-2}, PRF1 (perforin 1) [NCBI Gene 5551] {aka HPLH2, P1, PFP}, DEFB103B (defensin beta 103B) [NCBI Gene 55894] {aka BD-3, DEFB-3, DEFB103, DEFB3, HBD-3, HBD3}, KRT16 (keratin 16) [NCBI Gene 3868] {aka CK16, FNEPPK, K16, K1CP, KRT16A, NEPPK}
- **Diseases:** Brain Heart Infusion (MESH:D000075662), organ dysfunction (MESH:D009102), autoimmune diseases (MESH:D001327), malformation (MESH:C564254), chronic (MESH:D002908), foetal anomalies (MESH:D000013), immunodeficiency (MESH:D007153), AF (MESH:D004619), infection (MESH:D007239), cardiovascular conditions (MESH:D002318), sterility (MESH:D007246), endocrine/metabolic disorders (MESH:D004700), placentitis (MESH:D010922)
- **Chemicals:** water (MESH:D014867), polystyrene (MESH:D011137), CO2 (MESH:D002245), agarose (MESH:D012685), BHI broth (-), L-proline (MESH:D011392), phosphate (MESH:D010710), AMP (MESH:D000089882), O2 (MESH:D010100), sulfate (MESH:D013431), amino acids (MESH:D000596), thiamin (MESH:D013831), agar (MESH:D000362), L-phenylalanine (MESH:D010649), L-serine (MESH:D012694), carbon (MESH:D002244)
- **Species:** Rothia mucilaginosa (species) [taxon 43675], Micrococcus luteus (species) [taxon 1270], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bacillus licheniformis (species) [taxon 1402], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Equus caballus (domestic horse, species) [taxon 9796], Cellulosimicrobium funkei (species) [taxon 264251], Fusobacterium periodonticum (species) [taxon 860], Prevotella melaninogenica (species) [taxon 28132], Exiguobacterium profundum (species) [taxon 307643], Actinomycetota (actinobacteria, phylum) [taxon 201174], Bacillus (genus) [taxon 55087], Bacteroidia (class) [taxon 200643], Haemophilus haemolyticus (species) [taxon 726], Phyllobacterium zundukense (species) [taxon 1867719], Staphylococcus lugdunensis (species) [taxon 28035], Solibacillus isronensis (species) [taxon 412383], Cutibacterium acnes (species) [taxon 1747], Fusobacteriia (class) [taxon 203490], Bacillus subtilis (species) [taxon 1423], Phyllobacterium sp. (species) [taxon 1871046], Kocuria rhizophila (species) [taxon 72000], Escherichia coli (E. coli, species) [taxon 562], Amycolatopsis pretoriensis (species) [taxon 218821], Bacillus altitudinis (species) [taxon 293387], Lactobacillus mulieris (species) [taxon 2508708], Cutibacterium (genus) [taxon 1912216], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Chryseobacterium indologenes (species) [taxon 253], Homo sapiens (human, species) [taxon 9606], Acinetobacter ursingii (species) [taxon 108980], Staphylococcus epidermidis (species) [taxon 1282]

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Source: https://tomesphere.com/paper/PMC12918369