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263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance

BACKGROUND: Bacterial vaginosis (BV) is the most common vaginal infection among reproductive-aged women worldwide. It is associated with multiple adverse obstetric and gynecologic outcomes, yet its etiology remains unknown. BV is characterized by a decrease in protective lactobacilli (e.g., Lactobac...

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Autores principales: Elnaggar, Jacob H, Taylor, Christopher M, Ardizzone, Caleb M, Aaron, Kristal J, Eastlund, Isaac C, Graves, Keonte J, Luo, Meng, Quayle, Alison J, Cerca, Nuno, Muzny, Christina A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677015/
http://dx.doi.org/10.1093/ofid/ofad500.335
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author Elnaggar, Jacob H
Taylor, Christopher M
Ardizzone, Caleb M
Aaron, Kristal J
Eastlund, Isaac C
Graves, Keonte J
Luo, Meng
Quayle, Alison J
Cerca, Nuno
Muzny, Christina A
author_facet Elnaggar, Jacob H
Taylor, Christopher M
Ardizzone, Caleb M
Aaron, Kristal J
Eastlund, Isaac C
Graves, Keonte J
Luo, Meng
Quayle, Alison J
Cerca, Nuno
Muzny, Christina A
author_sort Elnaggar, Jacob H
collection PubMed
description BACKGROUND: Bacterial vaginosis (BV) is the most common vaginal infection among reproductive-aged women worldwide. It is associated with multiple adverse obstetric and gynecologic outcomes, yet its etiology remains unknown. BV is characterized by a decrease in protective lactobacilli (e.g., Lactobacillus crispatus), and a substantial increase in BV-associated bacteria (BVAB), particularly Gardnerella vaginalis. We investigated the vaginal microbiota to identify changes prior to, during, and immediately after incident BV (iBV). METHODS: Non-pregnant sexually active women who have sex with men ages 18-45 with normal baseline vaginal microbiota (no Amsel criteria, Nugent score 0-3) were enrolled and followed for iBV using twice-daily self-collected vaginal specimens. 16S rRNA gene sequencing was performed on specimens collected during the 14 days prior to BV (pre-BV), during BV (Nugent score 7-10), and days post-BV among cases. A similar number of specimens from age, race, and menstrual cycle day matched controls maintaining normal vaginal microbiota were also sequenced. qPCR was also performed on all specimens to determine total bacterial burden and inferred absolute abundance (IAA) of key vaginal bacteria, particularly G. vaginalis, L. crispatus, and L. iners. RESULTS: Vaginal specimens from 5 BV cases (n=169) and 5 matched controls (n=169; pre-BV [n=121], during BV [n=32], and post-BV [n=15]) were analyzed. Overall, a significantly higher bacterial burden was observed in specimens from BV cases compared to matched controls (Fig 1A). In BV cases, specimens collected on the day of BV had a significantly lower bacterial burden than specimens collected pre- and post-BV (Fig 1B). When comparing changes in the IAA of our vaginal bacteria of interest, we observed significantly higher amounts of G. vaginalis during BV (Fig 1C). There was a significant decrease in the IAA of L. crispatus during BV (Fig 1D), whereas L. iners IAA increased in post-BV (Fig 1E). Comparing qPCR and inferred absolute abundance (IAA) between vaginal specimens collected from women with incident BV (cases) and healthy controls maintaining normal vaginal microbiota. [Figure: see text] A, B. qPCR derived total bacterial burden between vaginal specimens from incident BV cases and healthy controls. C- E. inferred absolute abundance (IAA) of G. vaginalis, L. crispatus, and L. iners between vaginal specimens from incident BV cases and healthy controls. A, C. Mann Whitney test; B, D, E. Kruskal-Wallis test *p≤ 0.05, **p≤ 0.01, ***p≤ 0.001, ****p≤ 0.0001. CONCLUSION: These preliminary results support the hypothesis that a sequence of changes in the abundance of key vaginal bacteria occur prior to BV. During BV, we observed an increase in G. vaginalis while protective L. crispatus decreased, and L iners increased after BV. We anticipate expanding this analysis to include additional key BVAB. DISCLOSURES: Christina A. Muzny, MD, MSPH, Abbott Molecular: Grant/Research Support|Abbott Molecular: Honoraria|BioNTech: Advisor/Consultant|Cepheid: Advisor/Consultant|Cepheid: Honoraria|Elsevier: Honoraria|Gilead: Grant/Research Support|Lupin Pharmaceuticals: Grant/Research Support|Roche: Honoraria|Scynexis: Advisor/Consultant|Scynexis: Honoraria|Visby Medical: Honoraria
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spelling pubmed-106770152023-11-27 263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance Elnaggar, Jacob H Taylor, Christopher M Ardizzone, Caleb M Aaron, Kristal J Eastlund, Isaac C Graves, Keonte J Luo, Meng Quayle, Alison J Cerca, Nuno Muzny, Christina A Open Forum Infect Dis Abstract BACKGROUND: Bacterial vaginosis (BV) is the most common vaginal infection among reproductive-aged women worldwide. It is associated with multiple adverse obstetric and gynecologic outcomes, yet its etiology remains unknown. BV is characterized by a decrease in protective lactobacilli (e.g., Lactobacillus crispatus), and a substantial increase in BV-associated bacteria (BVAB), particularly Gardnerella vaginalis. We investigated the vaginal microbiota to identify changes prior to, during, and immediately after incident BV (iBV). METHODS: Non-pregnant sexually active women who have sex with men ages 18-45 with normal baseline vaginal microbiota (no Amsel criteria, Nugent score 0-3) were enrolled and followed for iBV using twice-daily self-collected vaginal specimens. 16S rRNA gene sequencing was performed on specimens collected during the 14 days prior to BV (pre-BV), during BV (Nugent score 7-10), and days post-BV among cases. A similar number of specimens from age, race, and menstrual cycle day matched controls maintaining normal vaginal microbiota were also sequenced. qPCR was also performed on all specimens to determine total bacterial burden and inferred absolute abundance (IAA) of key vaginal bacteria, particularly G. vaginalis, L. crispatus, and L. iners. RESULTS: Vaginal specimens from 5 BV cases (n=169) and 5 matched controls (n=169; pre-BV [n=121], during BV [n=32], and post-BV [n=15]) were analyzed. Overall, a significantly higher bacterial burden was observed in specimens from BV cases compared to matched controls (Fig 1A). In BV cases, specimens collected on the day of BV had a significantly lower bacterial burden than specimens collected pre- and post-BV (Fig 1B). When comparing changes in the IAA of our vaginal bacteria of interest, we observed significantly higher amounts of G. vaginalis during BV (Fig 1C). There was a significant decrease in the IAA of L. crispatus during BV (Fig 1D), whereas L. iners IAA increased in post-BV (Fig 1E). Comparing qPCR and inferred absolute abundance (IAA) between vaginal specimens collected from women with incident BV (cases) and healthy controls maintaining normal vaginal microbiota. [Figure: see text] A, B. qPCR derived total bacterial burden between vaginal specimens from incident BV cases and healthy controls. C- E. inferred absolute abundance (IAA) of G. vaginalis, L. crispatus, and L. iners between vaginal specimens from incident BV cases and healthy controls. A, C. Mann Whitney test; B, D, E. Kruskal-Wallis test *p≤ 0.05, **p≤ 0.01, ***p≤ 0.001, ****p≤ 0.0001. CONCLUSION: These preliminary results support the hypothesis that a sequence of changes in the abundance of key vaginal bacteria occur prior to BV. During BV, we observed an increase in G. vaginalis while protective L. crispatus decreased, and L iners increased after BV. We anticipate expanding this analysis to include additional key BVAB. DISCLOSURES: Christina A. Muzny, MD, MSPH, Abbott Molecular: Grant/Research Support|Abbott Molecular: Honoraria|BioNTech: Advisor/Consultant|Cepheid: Advisor/Consultant|Cepheid: Honoraria|Elsevier: Honoraria|Gilead: Grant/Research Support|Lupin Pharmaceuticals: Grant/Research Support|Roche: Honoraria|Scynexis: Advisor/Consultant|Scynexis: Honoraria|Visby Medical: Honoraria Oxford University Press 2023-11-27 /pmc/articles/PMC10677015/ http://dx.doi.org/10.1093/ofid/ofad500.335 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Elnaggar, Jacob H
Taylor, Christopher M
Ardizzone, Caleb M
Aaron, Kristal J
Eastlund, Isaac C
Graves, Keonte J
Luo, Meng
Quayle, Alison J
Cerca, Nuno
Muzny, Christina A
263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance
title 263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance
title_full 263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance
title_fullStr 263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance
title_full_unstemmed 263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance
title_short 263. A preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qPCR and inferred absolute abundance
title_sort 263. a preliminary analysis of vaginal microbial changes prior to incident bacterial vaginosis as determined by qpcr and inferred absolute abundance
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677015/
http://dx.doi.org/10.1093/ofid/ofad500.335
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