Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model
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Department of Obstetrics and Gynecology, College of Medicine-Phoenix, University of ArizonaDepartment of Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona
Department of Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona
Issue Date
2021
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Nature ResearchCitation
Salliss, M. E., Maarsingh, J. D., Garza, C., Łaniewski, P., & Herbst-Kralovetz, M. M. (2021). Veillonellaceae family members uniquely alter the cervical metabolic microenvironment in a human three-dimensional epithelial model. Npj Biofilms and Microbiomes, 7(1).Journal
npj Biofilms and MicrobiomesRights
Copyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.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. © 2021, The Author(s).Note
Open access journalISSN
2055-5008Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1038/s41522-021-00229-0
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Except where otherwise noted, this item's license is described as Copyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.