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Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model
Bacterial vaginosis (BV) is a gynecologic disorder characterized by a shift in cervicovaginal microbiota from Lactobacillus spp. dominance to a polymicrobial biofilm composed of diverse anaerobes. We utilized a well-characterized human three-dimensional cervical epithelial cell model in conjunction...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8260719/ https://www.ncbi.nlm.nih.gov/pubmed/34230496 http://dx.doi.org/10.1038/s41522-021-00229-0 |
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author | Salliss, Mary E. Maarsingh, Jason D. Garza, Camryn Łaniewski, Paweł Herbst-Kralovetz, Melissa M. |
author_facet | Salliss, Mary E. Maarsingh, Jason D. Garza, Camryn Łaniewski, Paweł Herbst-Kralovetz, Melissa M. |
author_sort | Salliss, Mary E. |
collection | PubMed |
description | Bacterial vaginosis (BV) is a gynecologic disorder characterized by a shift in cervicovaginal microbiota from Lactobacillus spp. dominance to a polymicrobial biofilm composed of diverse anaerobes. We utilized a well-characterized human three-dimensional cervical epithelial cell model in conjunction with untargeted metabolomics and immunoproteomics analyses to determine the immunometabolic contribution of three members of the Veillonellaceae family: Veillonella atypica, Veillonella montpellierensis and Megasphaera micronuciformis at this site. We found that Veillonella spp. infections induced significant elevation of polyamines. M. micronuciformis infections significantly increased soluble inflammatory mediators, induced moderate levels of cell cytotoxicity, and accumulation of cell membrane lipids relative to Veillonella spp. Notably, both V. atypica and V. montpellierensis infections resulted in consumption of lactate, a key metabolite linked to gynecologic and reproductive health. Collectively our approach and data provide unique insights into the specific contributions of Veillonellaceae members to the pathogenesis of BV and women’s health. |
format | Online Article Text |
id | pubmed-8260719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82607192021-07-23 Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model Salliss, Mary E. Maarsingh, Jason D. Garza, Camryn Łaniewski, Paweł Herbst-Kralovetz, Melissa M. NPJ Biofilms Microbiomes Article Bacterial vaginosis (BV) is a gynecologic disorder characterized by a shift in cervicovaginal microbiota from Lactobacillus spp. dominance to a polymicrobial biofilm composed of diverse anaerobes. We utilized a well-characterized human three-dimensional cervical epithelial cell model in conjunction with untargeted metabolomics and immunoproteomics analyses to determine the immunometabolic contribution of three members of the Veillonellaceae family: Veillonella atypica, Veillonella montpellierensis and Megasphaera micronuciformis at this site. We found that Veillonella spp. infections induced significant elevation of polyamines. M. micronuciformis infections significantly increased soluble inflammatory mediators, induced moderate levels of cell cytotoxicity, and accumulation of cell membrane lipids relative to Veillonella spp. Notably, both V. atypica and V. montpellierensis infections resulted in consumption of lactate, a key metabolite linked to gynecologic and reproductive health. Collectively our approach and data provide unique insights into the specific contributions of Veillonellaceae members to the pathogenesis of BV and women’s health. Nature Publishing Group UK 2021-07-06 /pmc/articles/PMC8260719/ /pubmed/34230496 http://dx.doi.org/10.1038/s41522-021-00229-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Salliss, Mary E. Maarsingh, Jason D. Garza, Camryn Łaniewski, Paweł Herbst-Kralovetz, Melissa M. Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
title | Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
title_full | Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
title_fullStr | Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
title_full_unstemmed | Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
title_short | Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
title_sort | veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8260719/ https://www.ncbi.nlm.nih.gov/pubmed/34230496 http://dx.doi.org/10.1038/s41522-021-00229-0 |
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