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Extracellular vesicles from vaginal Gardnerella vaginalis and Mobiluncus mulieris contain distinct proteomic cargo and induce inflammatory pathways.
Joseph, Andrea; Anton, Lauren; Guan, Yuxia; Ferguson, Briana; Mirro, Isabella; Meng, Nova; France, Michael; Ravel, Jacques; Elovitz, Michal A.
  • Joseph A; Women's Biomedical Research Institute, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA. andrea.joseph@mssm.edu.
  • Anton L; Department of Obstetrics, Gynecology and Reproductive Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA. andrea.joseph@mssm.edu.
  • Guan Y; Center for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, 19104, USA.
  • Ferguson B; Center for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, 19104, USA.
  • Mirro I; Center for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, 19104, USA.
  • Meng N; Center for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, 19104, USA.
  • France M; Center for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, PA, 19104, USA.
  • Ravel J; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
  • Elovitz MA; Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
NPJ Biofilms Microbiomes ; 10(1): 28, 2024 Mar 21.
Article en En | MEDLINE | ID: mdl-38514622
ABSTRACT
Colonization of the vaginal space with bacteria such as Gardnerella vaginalis and Mobiluncus mulieris is associated with increased risk for STIs, bacterial vaginosis, and preterm birth, while Lactobacillus crispatus is associated with optimal reproductive health. Although host-microbe interactions are hypothesized to contribute to reproductive health and disease, the bacterial mediators that are critical to this response remain unclear. Bacterial extracellular vesicles (bEVs) are proposed to participate in host-microbe communication by providing protection of bacterial cargo, delivery to intracellular targets, and ultimately induction of immune responses from the host. We evaluated the proteome of bEVs produced in vitro from G. vaginalis, M. mulieris, and L. crispatus, identifying specific proteins of immunologic interest. We found that bEVs from each bacterial species internalize within cervical and vaginal epithelial cells, and that epithelial and immune cells express a multi-cytokine response when exposed to bEVs from G. vaginalis and M. mulieris but not L. crispatus. Further, we demonstrate that the inflammatory response induced by G. vaginalis and M. mulieris bEVs is TLR2-specific. Our results provide evidence that vaginal bacteria communicate with host cells through secreted bEVs, revealing a mechanism by which bacteria lead to adverse reproductive outcomes associated with inflammation. Elucidating host-microbe interactions in the cervicovaginal space will provide further insight into the mechanisms contributing to microbiome-mediated adverse outcomes and may reveal new therapeutic targets.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nacimiento Prematuro / Vesículas Extracelulares Límite: Female / Humans / Newborn Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nacimiento Prematuro / Vesículas Extracelulares Límite: Female / Humans / Newborn Idioma: En Año: 2024 Tipo del documento: Article