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Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis

The role of neutrophils relative to vaginal dysbiosis is unclear. We hypothesize that bacterial vaginosis (BV)-associated bacteria may induce the activation and accumulation of mucosal neutrophils within the female reproductive tract (FRT), resulting in epithelial barrier damage. We collected endoce...

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Autores principales: Cheu, Ryan K., Mohammadi, Avid, Schifanella, Luca, Broedlow, Courtney, Driscoll, Connor B., Miller, Charlene J., Reeves, R. Keith, Yudin, Mark H., Hensley-McBain, Tiffany, Kaul, Rupert, Klatt, Nichole R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580658/
https://www.ncbi.nlm.nih.gov/pubmed/36303633
http://dx.doi.org/10.3389/frph.2022.876729
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author Cheu, Ryan K.
Mohammadi, Avid
Schifanella, Luca
Broedlow, Courtney
Driscoll, Connor B.
Miller, Charlene J.
Reeves, R. Keith
Yudin, Mark H.
Hensley-McBain, Tiffany
Kaul, Rupert
Klatt, Nichole R.
author_facet Cheu, Ryan K.
Mohammadi, Avid
Schifanella, Luca
Broedlow, Courtney
Driscoll, Connor B.
Miller, Charlene J.
Reeves, R. Keith
Yudin, Mark H.
Hensley-McBain, Tiffany
Kaul, Rupert
Klatt, Nichole R.
author_sort Cheu, Ryan K.
collection PubMed
description The role of neutrophils relative to vaginal dysbiosis is unclear. We hypothesize that bacterial vaginosis (BV)-associated bacteria may induce the activation and accumulation of mucosal neutrophils within the female reproductive tract (FRT), resulting in epithelial barrier damage. We collected endocervical cytobrushes from women with and without BV and assessed bacteria community type and frequency/functional phenotypes of neutrophils. We performed in vitro whole blood co-cultures with BV-associated bacteria and healthy vaginal commensals and assessed their impact on epithelial integrity using transepithelial electrical resistance. We demonstrated increased neutrophil frequency (p < 0.0001), activation (p < 0.0001), and prolonged lifespan (p < 0.0001) in the cytobrushes from women with non-Lactobacillus dominant (nLD) communities. Our in vitro co-cultures confirmed these results and identified significant barrier damage in the presence of neutrophils and G. vaginalis. Here, we demonstrate that BV-associated bacteria induce neutrophil activation and increase lifespan, potentially causing accumulation in the FRT and epithelial barrier damage.
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spelling pubmed-95806582022-10-26 Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis Cheu, Ryan K. Mohammadi, Avid Schifanella, Luca Broedlow, Courtney Driscoll, Connor B. Miller, Charlene J. Reeves, R. Keith Yudin, Mark H. Hensley-McBain, Tiffany Kaul, Rupert Klatt, Nichole R. Front Reprod Health Reproductive Health The role of neutrophils relative to vaginal dysbiosis is unclear. We hypothesize that bacterial vaginosis (BV)-associated bacteria may induce the activation and accumulation of mucosal neutrophils within the female reproductive tract (FRT), resulting in epithelial barrier damage. We collected endocervical cytobrushes from women with and without BV and assessed bacteria community type and frequency/functional phenotypes of neutrophils. We performed in vitro whole blood co-cultures with BV-associated bacteria and healthy vaginal commensals and assessed their impact on epithelial integrity using transepithelial electrical resistance. We demonstrated increased neutrophil frequency (p < 0.0001), activation (p < 0.0001), and prolonged lifespan (p < 0.0001) in the cytobrushes from women with non-Lactobacillus dominant (nLD) communities. Our in vitro co-cultures confirmed these results and identified significant barrier damage in the presence of neutrophils and G. vaginalis. Here, we demonstrate that BV-associated bacteria induce neutrophil activation and increase lifespan, potentially causing accumulation in the FRT and epithelial barrier damage. Frontiers Media S.A. 2022-07-13 /pmc/articles/PMC9580658/ /pubmed/36303633 http://dx.doi.org/10.3389/frph.2022.876729 Text en Copyright © 2022 Cheu, Mohammadi, Schifanella, Broedlow, Driscoll, Miller, Reeves, Yudin, Hensley-McBain, Kaul and Klatt. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Reproductive Health
Cheu, Ryan K.
Mohammadi, Avid
Schifanella, Luca
Broedlow, Courtney
Driscoll, Connor B.
Miller, Charlene J.
Reeves, R. Keith
Yudin, Mark H.
Hensley-McBain, Tiffany
Kaul, Rupert
Klatt, Nichole R.
Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis
title Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis
title_full Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis
title_fullStr Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis
title_full_unstemmed Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis
title_short Altered Innate Immunity and Damaged Epithelial Integrity in Vaginal Microbial Dysbiosis
title_sort altered innate immunity and damaged epithelial integrity in vaginal microbial dysbiosis
topic Reproductive Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580658/
https://www.ncbi.nlm.nih.gov/pubmed/36303633
http://dx.doi.org/10.3389/frph.2022.876729
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