Evidence map›Paper›PMID 42743328›Full record

ArticlePLoS computational biology2026

Predicting bacterial vaginosis incidence using artificial neural networks.

Jacob H Elnaggar, John W Lammons, Caleb M Ardizzone, Kristal J Aaron, Clayton Jacobs, Keonte J Graves, Sheridan D George, Megan Amerson-Brown, Meng Luo, Ashutosh Tamhane and 6 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Jacob H ElnaggarDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.
John W LammonsDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.ORCID https://orcid.org/0009-0002-8892-4576
Caleb M ArdizzoneDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.
Kristal J AaronDivision of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Clayton JacobsDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.
Keonte J GravesDivision of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Sheridan D GeorgeDivision of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID https://orcid.org/0009-0000-7420-9753
Megan Amerson-BrownDivision of Laboratory Science, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID https://orcid.org/0000-0002-1545-7826
Meng LuoDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.
Ashutosh TamhaneDivision of Nephrology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Paweł ŁaniewskiDepartment of Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona, United States of America.
Alison J QuayleDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.
Melissa M Herbst-KralovetzDepartment of Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona, United States of America.
Nuno CercaCentre of Biological Engineering, Laboratory of Research in Biofilms Rosário Oliveira, Minho University, Braga, Portugal.
Christina A MuznyDivision of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Christopher M TaylorDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.ORCID https://orcid.org/0000-0002-7983-5275

Funding

National Dissemination of I-Corps@NCATS: Accelerating Translation through CommercializationUL1TR003096 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GUTIERREZ, ORLANDO M, KIMBERLY, ROBERT P. · 2019 to 2023
$43.6M
Uranium as an Environmental Risk Factor for Cancer Among the NavajoU54CA143924 · NCI · UNIVERSITY OF ARIZONA · PI Melissa Marie Herbst-Kralovetz, JUANITA L. MERCHANT · 2009 to 2026
$26.7M
Immunology and Infectious Diseases Training ProgramT32AI060519 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI MARK H KAPLAN · 2004 to 2026
$6.0M
Microbial Interactions between Gardnerella, Prevotella, and Atopobium Prior to Incident Bacterial VaginosisR01AI146065 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MUZNY, CHRISTINA A · 2020 to 2024
$3.2M
Pathogenesis of Bacterial Vaginosis in Women Who Have Sex with WomenK23AI106957 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MUZNY, CHRISTINA A · 2014 to 2018
$873k
NCATS NIH HHS UL1 TR003096NCI NIH HHS U54 CA143924NIAID NIH HHS K23 AI106957NIAID NIH HHS R01 AI146065NIAID NIH HHS T32 AI060519
6 · The paper itself

Abstract

backgroundBacterial vaginosis (BV) is a vaginal dysbiosis associated with adverse reproductive and infectious outcomes. Current diagnostics identify BV after symptom onset. We evaluated whether artificial neural network (ANN) models of the vaginal microbiome could predict incident BV (iBV) up to 14 days before clinical diagnosis.

methodsANNs were trained using 16S rRNA gene sequencing data from 1,201 longitudinal vaginal specimens collected from 58 women across two prospective cohorts. Models classified individual specimens as pre-iBV or healthy using the relative abundance of vaginal bacterial taxa. Model performance was assessed using a held-out participant-level test set, participant-level cross-validation, and external validation. SHAP analysis was used to identify taxa associated with model predictions.

resultsOn the held-out participant-level test set, the ANN achieved 93% accuracy (AUC = 0.97, sensitivity = 95%, specificity = 92%). Models using only five taxa (Lactobacillus crispatus, Gardnerella spp., L. iners, L. mulieris, and Megamonas spp.) maintained >91% accuracy, sensitivity, and specificity. SHAP analysis identified Lactobacillus spp. and Gardnerella spp. as the taxa most strongly associated with model predictions. Participant-level cross-validation produced lower and more variable performance (AUC = 0.826 ± 0.076; accuracy = 71.5% ± 8.2%), while external validation achieved approximately 80% balanced accuracy.

interpretationVaginal microbiome composition contains predictive information that can identify women at risk of iBV before clinical onset. Lower performance during participant-level cross-validation and external validation indicates that additional validation in larger, more diverse cohorts is required before clinical implementation.

Indexed as

Neural Networks, ComputerVaginosis, BacterialComputational BiologyFemaleHumansIncidenceLactobacillusMicrobiotaPrediction AlgorithmsRNA, Ribosomal, 16SVaginaRNA, Ribosomal, 16S

Identifiers

PMID42743328
PMCPMC13592708

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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.