ArticleBMC microbiology2025
Inferred bi-directional interactions between vaginal microbiota, metabolome and persistent HPV infection accompanied by high-grade cervical intraepithelial neoplasia.
Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Exploring Cervical Cancer-Associated Vaginal and Cervical Microbiota via 16S rRNA Sequencing.MicrobiologyOpen · 2026Article
- Vaginal Microbiota Composition and HPV Genotype-Specific CIN2+ Risk: A Cross-Sectional Study.Diagnostics (Basel, Switzerland) · 2026Article
- Microbiome-Metabolome Crosstalk in HPV Pathogenesis: From Ecosystem Dynamics to Translational Biomarkers.Computational and structural biotechnology journal · 2026Review
- The implications and mechanisms of vaginal microbiota metabolites on cervical cancer progression.Frontiers in cellular and infection microbiology · 2026Review
- HPV vaccination associates withFrontiers in microbiology · 2026Article
- Vaginal Microecological Imbalance, Human Papillomavirus Infection, and Cervical Carcinogenesis: Mechanisms and Clinical Implications.International journal of general medicine · 2026Review
- Lactobacillus-Dominated Cervical Microbiota Revealed by Long-Read 16S rRNA Sequencing: A Greek Pilot Study.Genes · 2025Article
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Authors and funding
7 authors.
Funding
Abstract
backgroundVaginal microbiota (VM) links to the risk of persistent HPV infection and the progression of cervical intraepithelial neoplasia (CIN). However, a comprehensive understanding of concurrent alterations in VM and metabolome associated with that risk remains elusive in population-based studies, particularly among Chinese women.
methodsThis study conducted an extensive analysis of VM and metabolome profiles in a cohort of 56 Chinese women, classified into HPV_C (natural clearance of HPV, n = 18) and HPV_PH(persistent HPV infection accompanied by high-grade CIN, n = 38), based on the result of 3-6 months follow-up visits.
resultsOur analysis revealed a higher prevalence of Lactobacillus-dominated samples in the HPV_C cohort. Notably, the vaginal metabolome exhibited a significant interaction with VM, with Lactobacillus emerging as a pivotal influencer. We identified 386 metabolites that significantly differentiated between HPV_C and HPV_PH groups, of which 364 were associated with VM components such as Lactobacillus, Hoylesella, Fannyhessea and Megasphaera. Further examination showed that 66 of these 364 metabolites positively correlated with Lactobacillus, including citric acid, DL-beta-Leucine, Xanoic acid and Norcholic acid. Conversely, 19 metabolites, including HPV_PH enriched maltotriose and N-Acetyl-L-aspartic acid, negatively correlated with Lactobacillus. Further analysis suggested potential bi-directional modulation between VM and persistent HPV infection accompanied by high-grade, being partially mediated by vaginal metabolites.
conclusionsThis study provides additional insights into the correlations between concurrent alterations in VM and metabolome associated with persistent HPV infection accompanied by high-grade CIN.
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