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Follicular fluid bacterial DNA linked to IVF fertilization failure in exploratory cohort

Follicular fluid bacterial DNA linked to IVF fertilization failure in exploratory cohort
Photo by National Institute of Allergy and Infectious Diseases / Unsplash
Key Takeaway
Consider follicular fluid bacterial DNA as a potential marker for IVF fertilization failure, but interpret cautiously due to exploratory data.

This exploratory cohort study included 24 women undergoing IVF/ICSI treatment, analyzing follicular fluid microbial signatures. The intervention involved assessing bacterial DNA and total bacterial load in follicular fluid samples, comparing those associated with successful fertilization versus fertilization failure. The primary outcome was fertilization success or failure, with secondary outcomes including total bacterial load positivity, bacterial DNA presence above detection threshold, and detection of specific bacterial taxa.

Main results showed that bacterial DNA was present above the detection threshold in 39.6% of all follicular fluid samples. Total bacterial load positivity was higher in samples associated with fertilization failure (70.8%) compared to successful fertilization (8.3%). Specific bacterial taxa, such as Fannyhessea vaginae, Ureaplasma spp., and Lactobacillus spp., were more frequently detected in follicular fluid samples linked to failed fertilization, but no individual taxon showed a consistent association across all samples. Additionally, follicles from the same patient often differed in bacterial DNA presence, and absence of detectable bacterial DNA was associated with fertilization outcome.

Safety and tolerability data were not reported. Key limitations include the exploratory paired design, small sample size of 24 women, lack of consistent association of individual taxa across all samples, and the need for larger prospective studies to validate observations. Practice relevance highlights follicle-level heterogeneity in microbial DNA detection and underscores the importance of follicle-specific analyses in reproductive microbiome research, but findings are preliminary and biological mechanisms remain unclear.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundEmerging evidence suggests that the upper female reproductive tract is not sterile and that microbial signals within follicular fluid (FF) may influence oocyte competence. However, previous studies have largely relied on pooled FF samples or dominant follicles, limiting insight into follicle-specific associations with fertilization outcomes.MethodsIn this exploratory paired study, follicular fluid samples were collected from 24 women undergoing IVF/ICSI treatment. For each patient, two FF samples were analyzed individually: one associated with a fertilized oocyte, and one associated with an oocyte that failed fertilization. Bacterial DNA and total bacterial load (TBL) were assessed using quantitative real-time PCR targeting predefined microbial taxa.ResultsBacterial DNA above the predefined detection threshold was identified in 39.6% of all FF samples. Notably, within this exploratory cohort, FF samples associated with fertilization failure were more frequently TBL-positive compared with FF samples linked to successful fertilization (70.8% vs. 8.3%). Follicles from the same patient often differed in bacterial DNA presence, indicating substantial intra-individual variability. Several bacterial taxa, including Fannyhessea vaginae, Ureaplasma spp., and Lactobacillus spp., were more frequently detected in FF samples associated with failed fertilization; however, no individual taxon showed a consistent association with outcome across all samples.ConclusionIn this paired follicle-level analysis, the absence of detectable bacterial DNA in follicular fluid was associated with fertilization outcome. These findings highlight follicle-level heterogeneity in microbial DNA detection and underscore the importance of follicle-specific analyses in reproductive microbiome research. Larger prospective studies are required to validate these observations and to clarify the biological mechanisms underlying follicular microbial signals.
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