Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model

Abstract 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 con...

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Autores principales: Mary E. Salliss, Jason D. Maarsingh, Camryn Garza, Paweł Łaniewski, Melissa M. Herbst-Kralovetz
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/e4a05f8b51b64bc1a9965de6c1f4b3d7
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spelling oai:doaj.org-article:e4a05f8b51b64bc1a9965de6c1f4b3d72021-12-02T16:15:07ZVeillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model10.1038/s41522-021-00229-02055-5008https://doaj.org/article/e4a05f8b51b64bc1a9965de6c1f4b3d72021-07-01T00:00:00Zhttps://doi.org/10.1038/s41522-021-00229-0https://doaj.org/toc/2055-5008Abstract 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.Mary E. SallissJason D. MaarsinghCamryn GarzaPaweł ŁaniewskiMelissa M. Herbst-KralovetzNature PortfolioarticleMicrobial ecologyQR100-130ENnpj Biofilms and Microbiomes, Vol 7, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Microbial ecology
QR100-130
spellingShingle Microbial ecology
QR100-130
Mary E. Salliss
Jason D. Maarsingh
Camryn Garza
Paweł Łaniewski
Melissa M. Herbst-Kralovetz
Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model
description Abstract 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 article
author Mary E. Salliss
Jason D. Maarsingh
Camryn Garza
Paweł Łaniewski
Melissa M. Herbst-Kralovetz
author_facet Mary E. Salliss
Jason D. Maarsingh
Camryn Garza
Paweł Łaniewski
Melissa M. Herbst-Kralovetz
author_sort Mary E. Salliss
title 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_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_sort veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/e4a05f8b51b64bc1a9965de6c1f4b3d7
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