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    Vaginal microbiome-host interactions modeled in a human vagina-on-a-chip.

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    Author
    Mahajan, Gautam
    Doherty, Erin
    To, Tania
    Sutherland, Arlene
    Grant, Jennifer
    Junaid, Abidemi
    Gulati, Aakanksha
    LoGrande, Nina
    Izadifar, Zohreh
    Timilsina, Sanjay Sharma
    Horváth, Viktor
    Plebani, Roberto
    France, Michael
    Hood-Pishchany, Indriati
    Rakoff-Nahoum, Seth
    Kwon, Douglas S
    Goyal, Girija
    Prantil-Baun, Rachelle
    Ravel, Jacques
    Ingber, Donald E
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    Date
    2022-11-26
    Journal
    Microbiome
    Type
    Article
    
    Metadata
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    See at
    https://doi.org/10.1186/s40168-022-01400-1
    Abstract
    Background: A dominance of non-iners Lactobacillus species in the vaginal microbiome is optimal and strongly associated with gynecological and obstetric health, while the presence of diverse obligate or facultative anaerobic bacteria and a paucity in Lactobacillus species, similar to communities found in bacterial vaginosis (BV), is considered non-optimal and associated with adverse health outcomes. Various therapeutic strategies are being explored to modulate the composition of the vaginal microbiome; however, there is no human model that faithfully reproduces the vaginal epithelial microenvironment for preclinical validation of potential therapeutics or testing hypotheses about vaginal epithelium-microbiome interactions. Results: Here, we describe an organ-on-a-chip (organ chip) microfluidic culture model of the human vaginal mucosa (vagina chip) that is lined by hormone-sensitive, primary vaginal epithelium interfaced with underlying stromal fibroblasts, which sustains a low physiological oxygen concentration in the epithelial lumen. We show that the Vagina Chip can be used to assess colonization by optimal L. crispatus consortia as well as non-optimal Gardnerella vaginalis-containing consortia, and to measure associated host innate immune responses. Co-culture and growth of the L. crispatus consortia on-chip was accompanied by maintenance of epithelial cell viability, accumulation of D- and L-lactic acid, maintenance of a physiologically relevant low pH, and down regulation of proinflammatory cytokines. In contrast, co-culture of G. vaginalis-containing consortia in the vagina chip resulted in epithelial cell injury, a rise in pH, and upregulation of proinflammatory cytokines. Conclusion: This study demonstrates the potential of applying human organ chip technology to create a preclinical model of the human vaginal mucosa that can be used to better understand interactions between the vaginal microbiome and host tissues, as well as to evaluate the safety and efficacy of live biotherapeutics products.
    Rights/Terms
    © 2022. The Author(s).
    Identifier to cite or link to this item
    http://hdl.handle.net/10713/20268
    ae974a485f413a2113503eed53cd6c53
    10.1186/s40168-022-01400-1
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