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Molecular characterization of vaginal microbiota using a new 22-species qRT-PCR test to achieve a relative-abundance and species-based diagnosis of bacterial vaginosis.
Oyenihi, Ayodeji B; Haines, Ronald; Trama, Jason; Faro, Sebastian; Mordechai, Eli; Adelson, Martin E; Osei Sekyere, John.
Affiliation
  • Oyenihi AB; Institute for Biomarker Research, Medical Diagnostic Laboratories, Genesis Biotechnology Group, Hamilton, NJ, United States.
  • Haines R; Institute for Biomarker Research, Medical Diagnostic Laboratories, Genesis Biotechnology Group, Hamilton, NJ, United States.
  • Trama J; Institute for Biomarker Research, Medical Diagnostic Laboratories, Genesis Biotechnology Group, Hamilton, NJ, United States.
  • Faro S; Institute for Biomarker Research, Medical Diagnostic Laboratories, Genesis Biotechnology Group, Hamilton, NJ, United States.
  • Mordechai E; Memorial Women's Care, Houston, TX, United States.
  • Adelson ME; Institute for Biomarker Research, Medical Diagnostic Laboratories, Genesis Biotechnology Group, Hamilton, NJ, United States.
  • Osei Sekyere J; Institute for Biomarker Research, Medical Diagnostic Laboratories, Genesis Biotechnology Group, Hamilton, NJ, United States.
Front Cell Infect Microbiol ; 14: 1409774, 2024.
Article in En | MEDLINE | ID: mdl-39006741
ABSTRACT

Background:

Numerous bacteria are involved in the etiology of bacterial vaginosis (BV). Yet, current tests only focus on a select few. We therefore designed a new test targeting 22 BV-relevant species.

Methods:

Using 946 stored vaginal samples, a new qPCR test that quantitatively identifies 22 bacterial species was designed. The distribution and relative abundance of each species, α- and ß-diversities, correlation, and species co-existence were determined per sample. A diagnostic index was modeled from the data, trained, and tested to classify samples into BV-positive, BV-negative, or transitional BV.

Results:

The qPCR test identified all 22 targeted species with 95 - 100% sensitivity and specificity within 8 hours (from sample reception). Across most samples, Lactobacillus iners, Lactobacillus crispatus, Lactobacillus jensenii, Gardnerella vaginalis, Fannyhessea (Atopobium) vaginae, Prevotella bivia, and Megasphaera sp. type 1 were relatively abundant. BVAB-1 was more abundant and distributed than BVAB-2 and BVAB-3. No Mycoplasma genitalium was found. The inter-sample similarity was very low, and correlations existed between key species, which were used to model, train, and test a diagnostic index MDL-BV index. The MDL-BV index, using both species and relative abundance markers, classified samples into three vaginal microbiome states. Testing this index on our samples, 491 were BV-positive, 318 were BV-negative, and 137 were transitional BV. Although important differences in BV status were observed between different age groups, races, and pregnancy status, they were statistically insignificant.

Conclusion:

Using a diverse and large number of vaginal samples from different races and age groups, including pregnant women, the new qRT-PCR test and MDL-BV index efficiently diagnosed BV within 8 hours (from sample reception), using 22 BV-associated species.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Vagina / Gardnerella vaginalis / Vaginosis, Bacterial / Real-Time Polymerase Chain Reaction / Microbiota / Lactobacillus Limits: Adolescent / Adult / Female / Humans / Middle aged / Pregnancy Language: En Journal: Front Cell Infect Microbiol Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Vagina / Gardnerella vaginalis / Vaginosis, Bacterial / Real-Time Polymerase Chain Reaction / Microbiota / Lactobacillus Limits: Adolescent / Adult / Female / Humans / Middle aged / Pregnancy Language: En Journal: Front Cell Infect Microbiol Year: 2024 Type: Article Affiliation country: United States