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Interaction of Gardnerella vaginalis and Vaginolysin with the Apical versus Basolateral Face of a Three-Dimensional Model of Vaginal Epithelium
Studies have implicated as an important etiological agent in bacterial vaginosis (BV). It produces a cholesterol-dependent cytolysin, vaginolysin (VLY). In this study, we sought to characterize the interaction between vaginal epithelium, , and VLY using EpiVaginal tissues from MatTek. These tissues...
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Published in: | Infection and immunity 2019-04, Vol.87 (4) |
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description | Studies have implicated
as an important etiological agent in bacterial vaginosis (BV). It produces a cholesterol-dependent cytolysin, vaginolysin (VLY). In this study, we sought to characterize the interaction between vaginal epithelium,
, and VLY using EpiVaginal tissues from MatTek. These tissues are three-dimensional and have distinct apical and basolateral sides, enabling comparison of the effects of
and VLY following exposure to either side. We measured cytotoxicity, cytokine production, and bacterial growth, following apical versus basolateral exposure.
exhibited more-rapid growth in coculture with the tissue model when it was exposed to the apical side. VLY permeabilized cells on the basolateral side of the tissues but failed to permeabilize apical epithelial cells. Cytokine secretion in response to VLY and
also depended on the polarity of exposure. VLY did not cause significant changes in cytokine levels when exposed apically. Apical tissue challenge by
appeared to dampen the inflammatory response, as decreases in granulocyte-macrophage colony-stimulating factor (GM-CSF) (6.6-fold), RANTES (14.8-fold), and interferon gamma inducible protein 10 kDa (IP-10) (53-fold) and an increase in interleukin-1 receptor antagonist (IL-1ra) (5-fold) were observed.
,
normally colonizes the apical face of the vaginal epithelium. Results from this study suggest that while
may grow on the apical face of the vaginal epithelium, its VLY toxin does not target these cells in this model. This phenomenon could have important implications regarding colonization of the vagina by
and may suggest an explanation for the lack of an overt immune response to this organism. |
doi_str_mv | 10.1128/IAI.00646-18 |
format | article |
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as an important etiological agent in bacterial vaginosis (BV). It produces a cholesterol-dependent cytolysin, vaginolysin (VLY). In this study, we sought to characterize the interaction between vaginal epithelium,
, and VLY using EpiVaginal tissues from MatTek. These tissues are three-dimensional and have distinct apical and basolateral sides, enabling comparison of the effects of
and VLY following exposure to either side. We measured cytotoxicity, cytokine production, and bacterial growth, following apical versus basolateral exposure.
exhibited more-rapid growth in coculture with the tissue model when it was exposed to the apical side. VLY permeabilized cells on the basolateral side of the tissues but failed to permeabilize apical epithelial cells. Cytokine secretion in response to VLY and
also depended on the polarity of exposure. VLY did not cause significant changes in cytokine levels when exposed apically. Apical tissue challenge by
appeared to dampen the inflammatory response, as decreases in granulocyte-macrophage colony-stimulating factor (GM-CSF) (6.6-fold), RANTES (14.8-fold), and interferon gamma inducible protein 10 kDa (IP-10) (53-fold) and an increase in interleukin-1 receptor antagonist (IL-1ra) (5-fold) were observed.
,
normally colonizes the apical face of the vaginal epithelium. Results from this study suggest that while
may grow on the apical face of the vaginal epithelium, its VLY toxin does not target these cells in this model. This phenomenon could have important implications regarding colonization of the vagina by
and may suggest an explanation for the lack of an overt immune response to this organism.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.00646-18</identifier><identifier>PMID: 30692180</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacterial Proteins - metabolism ; Bacterial Toxins - metabolism ; Cellular Microbiology: Pathogen-Host Cell Molecular Interactions ; Epithelium - microbiology ; Female ; Gardnerella vaginalis - genetics ; Gardnerella vaginalis - growth & development ; Gardnerella vaginalis - metabolism ; Granulocyte-Macrophage Colony-Stimulating Factor - genetics ; Granulocyte-Macrophage Colony-Stimulating Factor - metabolism ; Humans ; Interleukin-18 - genetics ; Interleukin-18 - metabolism ; Vagina - microbiology ; Vagina - pathology ; Vaginosis, Bacterial - genetics ; Vaginosis, Bacterial - metabolism ; Vaginosis, Bacterial - microbiology ; Vaginosis, Bacterial - pathology</subject><ispartof>Infection and immunity, 2019-04, Vol.87 (4)</ispartof><rights>Copyright © 2019 American Society for Microbiology.</rights><rights>Copyright © 2019 American Society for Microbiology. 2019 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-7c6b459dde68b0d9c97783cb82e9a2ae74e9c6ba0271146fb03bc7020e8844593</citedby><cites>FETCH-LOGICAL-c384t-7c6b459dde68b0d9c97783cb82e9a2ae74e9c6ba0271146fb03bc7020e8844593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434120/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434120/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30692180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Young, Vincent B.</contributor><creatorcontrib>Garcia, Erin M</creatorcontrib><creatorcontrib>Kraskauskiene, Vita</creatorcontrib><creatorcontrib>Koblinski, Jennifer E</creatorcontrib><creatorcontrib>Jefferson, Kimberly K</creatorcontrib><title>Interaction of Gardnerella vaginalis and Vaginolysin with the Apical versus Basolateral Face of a Three-Dimensional Model of Vaginal Epithelium</title><title>Infection and immunity</title><addtitle>Infect Immun</addtitle><description>Studies have implicated
as an important etiological agent in bacterial vaginosis (BV). It produces a cholesterol-dependent cytolysin, vaginolysin (VLY). In this study, we sought to characterize the interaction between vaginal epithelium,
, and VLY using EpiVaginal tissues from MatTek. These tissues are three-dimensional and have distinct apical and basolateral sides, enabling comparison of the effects of
and VLY following exposure to either side. We measured cytotoxicity, cytokine production, and bacterial growth, following apical versus basolateral exposure.
exhibited more-rapid growth in coculture with the tissue model when it was exposed to the apical side. VLY permeabilized cells on the basolateral side of the tissues but failed to permeabilize apical epithelial cells. Cytokine secretion in response to VLY and
also depended on the polarity of exposure. VLY did not cause significant changes in cytokine levels when exposed apically. Apical tissue challenge by
appeared to dampen the inflammatory response, as decreases in granulocyte-macrophage colony-stimulating factor (GM-CSF) (6.6-fold), RANTES (14.8-fold), and interferon gamma inducible protein 10 kDa (IP-10) (53-fold) and an increase in interleukin-1 receptor antagonist (IL-1ra) (5-fold) were observed.
,
normally colonizes the apical face of the vaginal epithelium. Results from this study suggest that while
may grow on the apical face of the vaginal epithelium, its VLY toxin does not target these cells in this model. This phenomenon could have important implications regarding colonization of the vagina by
and may suggest an explanation for the lack of an overt immune response to this organism.</description><subject>Bacterial Proteins - metabolism</subject><subject>Bacterial Toxins - metabolism</subject><subject>Cellular Microbiology: Pathogen-Host Cell Molecular Interactions</subject><subject>Epithelium - microbiology</subject><subject>Female</subject><subject>Gardnerella vaginalis - genetics</subject><subject>Gardnerella vaginalis - growth & development</subject><subject>Gardnerella vaginalis - metabolism</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - genetics</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - metabolism</subject><subject>Humans</subject><subject>Interleukin-18 - genetics</subject><subject>Interleukin-18 - metabolism</subject><subject>Vagina - microbiology</subject><subject>Vagina - pathology</subject><subject>Vaginosis, Bacterial - genetics</subject><subject>Vaginosis, Bacterial - metabolism</subject><subject>Vaginosis, Bacterial - microbiology</subject><subject>Vaginosis, Bacterial - pathology</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkcFPHCEUxklTU7fam-eGYw-OAsMycDFZrdpNNF6sV8Iwb10aBlaY2ca_ov9yma6aeiIv38fve3kfQkeUnFDK5OlysTwhRHBRUfkBzShRsprPGfuIZoRQVam5aPbR55x_lZFzLj-h_ZoIxagkM_RnGQZIxg4uBhxX-NqkLkAC7w3emkcXjHcZm9Dhh2mK_jm7gH-7YY2HNeDFxlnj8RZSHjM-Nzl6M_E8vjIWJqDB9-sEUH13PYRcUop2Gzvwk_iwS8CXmwIE78b-EO2tjM_w5eU9QD-vLu8vflQ3d9fLi8VNZWvJh6qxouVz1XUgZEs6ZVXTyNq2koEyzEDDQRWLIayhlItVS-rWNoQRkJKXj_UBOttxN2PbQ2chDGVrvUmuN-lZR-P0eyW4tX6MWy14zSkjBfDtBZDi0wh50L3LdrpbgDhmzWijeK2E5MV6vLPaFHNOsHqLoURPHerSof7Xoaay2L_-v9qb-bW0-i9M_pol</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Garcia, Erin M</creator><creator>Kraskauskiene, Vita</creator><creator>Koblinski, Jennifer E</creator><creator>Jefferson, Kimberly K</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190401</creationdate><title>Interaction of Gardnerella vaginalis and Vaginolysin with the Apical versus Basolateral Face of a Three-Dimensional Model of Vaginal Epithelium</title><author>Garcia, Erin M ; Kraskauskiene, Vita ; Koblinski, Jennifer E ; Jefferson, Kimberly K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-7c6b459dde68b0d9c97783cb82e9a2ae74e9c6ba0271146fb03bc7020e8844593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Bacterial Proteins - metabolism</topic><topic>Bacterial Toxins - metabolism</topic><topic>Cellular Microbiology: Pathogen-Host Cell Molecular Interactions</topic><topic>Epithelium - microbiology</topic><topic>Female</topic><topic>Gardnerella vaginalis - genetics</topic><topic>Gardnerella vaginalis - growth & development</topic><topic>Gardnerella vaginalis - metabolism</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - genetics</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - metabolism</topic><topic>Humans</topic><topic>Interleukin-18 - genetics</topic><topic>Interleukin-18 - metabolism</topic><topic>Vagina - microbiology</topic><topic>Vagina - pathology</topic><topic>Vaginosis, Bacterial - genetics</topic><topic>Vaginosis, Bacterial - metabolism</topic><topic>Vaginosis, Bacterial - microbiology</topic><topic>Vaginosis, Bacterial - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garcia, Erin M</creatorcontrib><creatorcontrib>Kraskauskiene, Vita</creatorcontrib><creatorcontrib>Koblinski, Jennifer E</creatorcontrib><creatorcontrib>Jefferson, Kimberly K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garcia, Erin M</au><au>Kraskauskiene, Vita</au><au>Koblinski, Jennifer E</au><au>Jefferson, Kimberly K</au><au>Young, Vincent B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction of Gardnerella vaginalis and Vaginolysin with the Apical versus Basolateral Face of a Three-Dimensional Model of Vaginal Epithelium</atitle><jtitle>Infection and immunity</jtitle><addtitle>Infect Immun</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>87</volume><issue>4</issue><issn>0019-9567</issn><eissn>1098-5522</eissn><abstract>Studies have implicated
as an important etiological agent in bacterial vaginosis (BV). It produces a cholesterol-dependent cytolysin, vaginolysin (VLY). In this study, we sought to characterize the interaction between vaginal epithelium,
, and VLY using EpiVaginal tissues from MatTek. These tissues are three-dimensional and have distinct apical and basolateral sides, enabling comparison of the effects of
and VLY following exposure to either side. We measured cytotoxicity, cytokine production, and bacterial growth, following apical versus basolateral exposure.
exhibited more-rapid growth in coculture with the tissue model when it was exposed to the apical side. VLY permeabilized cells on the basolateral side of the tissues but failed to permeabilize apical epithelial cells. Cytokine secretion in response to VLY and
also depended on the polarity of exposure. VLY did not cause significant changes in cytokine levels when exposed apically. Apical tissue challenge by
appeared to dampen the inflammatory response, as decreases in granulocyte-macrophage colony-stimulating factor (GM-CSF) (6.6-fold), RANTES (14.8-fold), and interferon gamma inducible protein 10 kDa (IP-10) (53-fold) and an increase in interleukin-1 receptor antagonist (IL-1ra) (5-fold) were observed.
,
normally colonizes the apical face of the vaginal epithelium. Results from this study suggest that while
may grow on the apical face of the vaginal epithelium, its VLY toxin does not target these cells in this model. This phenomenon could have important implications regarding colonization of the vagina by
and may suggest an explanation for the lack of an overt immune response to this organism.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>30692180</pmid><doi>10.1128/IAI.00646-18</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bacterial Proteins - metabolism Bacterial Toxins - metabolism Cellular Microbiology: Pathogen-Host Cell Molecular Interactions Epithelium - microbiology Female Gardnerella vaginalis - genetics Gardnerella vaginalis - growth & development Gardnerella vaginalis - metabolism Granulocyte-Macrophage Colony-Stimulating Factor - genetics Granulocyte-Macrophage Colony-Stimulating Factor - metabolism Humans Interleukin-18 - genetics Interleukin-18 - metabolism Vagina - microbiology Vagina - pathology Vaginosis, Bacterial - genetics Vaginosis, Bacterial - metabolism Vaginosis, Bacterial - microbiology Vaginosis, Bacterial - pathology |
title | Interaction of Gardnerella vaginalis and Vaginolysin with the Apical versus Basolateral Face of a Three-Dimensional Model of Vaginal Epithelium |
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