Extracellular vesicles from vaginal Gardnerella vaginalis and Mobiluncus mulieris contain distinct proteomic cargo and induce inflammatory pathways.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-03-21 DOI:10.1038/s41522-024-00502-y
Andrea Joseph, Lauren Anton, Yuxia Guan, Briana Ferguson, Isabella Mirro, Nova Meng, Michael France, Jacques Ravel, Michal A Elovitz
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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.

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阴道加德纳菌和莫比伦菌的胞外囊泡含有不同的蛋白质组,并能诱导炎症途径。
阴道加德纳菌和阴道毛杆菌等细菌在阴道内的定植与性传播感染、细菌性阴道病和早产风险的增加有关,而脆片乳杆菌则与最佳生殖健康有关。虽然宿主与微生物之间的相互作用被认为有助于生殖健康和疾病,但对这种反应至关重要的细菌介质仍不清楚。细菌胞外囊泡(bEVs)被认为可通过保护细菌货物、向细胞内靶标输送以及最终诱导宿主的免疫反应来参与宿主与微生物的交流。我们评估了阴道球菌、毛霉菌和栗色球菌体外产生的 bEVs 的蛋白质组,确定了具有免疫学意义的特定蛋白质。我们发现,每种细菌的 bEVs 都能在宫颈和阴道上皮细胞内发生内化,当暴露于 G. vaginalis 和 M. mulieris 的 bEVs 而不是 L. crispatus 的 bEVs 时,上皮细胞和免疫细胞会表达多种细胞因子反应。此外,我们还证明了阴道杆菌和毛霉菌 bEV 诱导的炎症反应是 TLR2 特异性的。我们的研究结果提供了阴道细菌通过分泌的 bEV 与宿主细胞沟通的证据,揭示了细菌导致与炎症相关的不良生殖结果的机制。阐明宫颈阴道空间中宿主与微生物之间的相互作用将有助于进一步了解微生物介导不良后果的机制,并可能揭示新的治疗靶点。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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