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Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria
Vaginal dysbiosis in women reduces the abundance of Lactobacillus species and increases that of anaerobic fastidious bacteria. This dysbiotic condition in the vagina, called bacterial vaginosis (BV), can be symptomatic with odorous vaginal discharges or asymptomatic and affects a third of women of r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434177/ https://www.ncbi.nlm.nih.gov/pubmed/37347202 http://dx.doi.org/10.1128/spectrum.04676-22 |
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author | Osei Sekyere, John Oyenihi, Ayodeji B. Trama, Jason Adelson, Martin E. |
author_facet | Osei Sekyere, John Oyenihi, Ayodeji B. Trama, Jason Adelson, Martin E. |
author_sort | Osei Sekyere, John |
collection | PubMed |
description | Vaginal dysbiosis in women reduces the abundance of Lactobacillus species and increases that of anaerobic fastidious bacteria. This dysbiotic condition in the vagina, called bacterial vaginosis (BV), can be symptomatic with odorous vaginal discharges or asymptomatic and affects a third of women of reproductive age. Three unclassified bacterial species designated BV-associated bacteria 1, 2, and 3 (BVAB-1, -2, and -3) in 2005 were found to be highly preponderant in the vagina of females with BV. Here, we used sequence homology and phylogenetics analyses to identify the actual species of BVAB-1, -2, and -3 and found BVAB-1 to be Clostridiales genomosp. BVAB-1, BVAB-2 to be Oscillospiraceae bacterium strain CHIC02, and BVAB-3 to be Mageeibacillus indolicus, respectively. These are anaerobic and uncultured species that can be identified only through metagenomics. Long-read sequencing of BV specimens can also enable a genomic reassembly of these species’ genomes from metagenomes. Species-specific identification of these pathogens and the availability of their genomes from assembled metagenomes will advance our understanding of their biology, facilitate the design of sensitive diagnostics and drugs, and enhance the treatment of BV. IMPORTANCE For many years since 2005, BVAB, an important pathogen of the female vaginal tract that is associated with BV, has been identified using PCR without knowing its actual species. Without a full genome of these pathogens, a better understanding of their pathogenicity, treatment, resistance, and diagnostics cannot be reached. In this analysis, we use the DNA of BVAB-1, -2, and -3 to determine their actual species to enhance further research into their pathogenicity, resistance, diagnosis, and treatment. |
format | Online Article Text |
id | pubmed-10434177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-104341772023-08-18 Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria Osei Sekyere, John Oyenihi, Ayodeji B. Trama, Jason Adelson, Martin E. Microbiol Spectr Observation Vaginal dysbiosis in women reduces the abundance of Lactobacillus species and increases that of anaerobic fastidious bacteria. This dysbiotic condition in the vagina, called bacterial vaginosis (BV), can be symptomatic with odorous vaginal discharges or asymptomatic and affects a third of women of reproductive age. Three unclassified bacterial species designated BV-associated bacteria 1, 2, and 3 (BVAB-1, -2, and -3) in 2005 were found to be highly preponderant in the vagina of females with BV. Here, we used sequence homology and phylogenetics analyses to identify the actual species of BVAB-1, -2, and -3 and found BVAB-1 to be Clostridiales genomosp. BVAB-1, BVAB-2 to be Oscillospiraceae bacterium strain CHIC02, and BVAB-3 to be Mageeibacillus indolicus, respectively. These are anaerobic and uncultured species that can be identified only through metagenomics. Long-read sequencing of BV specimens can also enable a genomic reassembly of these species’ genomes from metagenomes. Species-specific identification of these pathogens and the availability of their genomes from assembled metagenomes will advance our understanding of their biology, facilitate the design of sensitive diagnostics and drugs, and enhance the treatment of BV. IMPORTANCE For many years since 2005, BVAB, an important pathogen of the female vaginal tract that is associated with BV, has been identified using PCR without knowing its actual species. Without a full genome of these pathogens, a better understanding of their pathogenicity, treatment, resistance, and diagnostics cannot be reached. In this analysis, we use the DNA of BVAB-1, -2, and -3 to determine their actual species to enhance further research into their pathogenicity, resistance, diagnosis, and treatment. American Society for Microbiology 2023-06-22 /pmc/articles/PMC10434177/ /pubmed/37347202 http://dx.doi.org/10.1128/spectrum.04676-22 Text en Copyright © 2023 Osei Sekyere et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Observation Osei Sekyere, John Oyenihi, Ayodeji B. Trama, Jason Adelson, Martin E. Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria |
title | Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria |
title_full | Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria |
title_fullStr | Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria |
title_full_unstemmed | Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria |
title_short | Species-Specific Analysis of Bacterial Vaginosis-Associated Bacteria |
title_sort | species-specific analysis of bacterial vaginosis-associated bacteria |
topic | Observation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434177/ https://www.ncbi.nlm.nih.gov/pubmed/37347202 http://dx.doi.org/10.1128/spectrum.04676-22 |
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