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The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection
The mechanism(s) by which Lactobacillus-dominated cervicovaginal microbiota provide a barrier to Chlamydia trachomatis infection remain(s) unknown. Here we evaluate the impact of different Lactobacillus spp. identified via culture-independent metataxonomic analysis of C. trachomatis-infected women o...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692509/ https://www.ncbi.nlm.nih.gov/pubmed/31409678 http://dx.doi.org/10.1128/mBio.01548-19 |
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author | Edwards, Vonetta L. Smith, Steven B. McComb, Elias J. Tamarelle, Jeanne Ma, Bing Humphrys, Michael S. Gajer, Pawel Gwilliam, Kathleen Schaefer, Alison M. Lai, Samuel K. Terplan, Mishka Mark, Katrina S. Brotman, Rebecca M. Forney, Larry J. Bavoil, Patrik M. Ravel, Jacques |
author_facet | Edwards, Vonetta L. Smith, Steven B. McComb, Elias J. Tamarelle, Jeanne Ma, Bing Humphrys, Michael S. Gajer, Pawel Gwilliam, Kathleen Schaefer, Alison M. Lai, Samuel K. Terplan, Mishka Mark, Katrina S. Brotman, Rebecca M. Forney, Larry J. Bavoil, Patrik M. Ravel, Jacques |
author_sort | Edwards, Vonetta L. |
collection | PubMed |
description | The mechanism(s) by which Lactobacillus-dominated cervicovaginal microbiota provide a barrier to Chlamydia trachomatis infection remain(s) unknown. Here we evaluate the impact of different Lactobacillus spp. identified via culture-independent metataxonomic analysis of C. trachomatis-infected women on C. trachomatis infection in a three-dimensional (3D) cervical epithelium model. Lactobacillus spp. that specifically produce d(−) lactic acid were associated with long-term protection against C. trachomatis infection, consistent with reduced protection associated with Lactobacillus iners, which does not produce this isoform, and with decreased epithelial cell proliferation, consistent with the observed prolonged protective effect. Transcriptomic analysis revealed that epigenetic modifications involving histone deacetylase-controlled pathways are integral to the cross talk between host and microbiota. These results highlight a fundamental mechanism whereby the cervicovaginal microbiota modulates host functions to protect against C. trachomatis infection. |
format | Online Article Text |
id | pubmed-6692509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-66925092019-08-21 The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection Edwards, Vonetta L. Smith, Steven B. McComb, Elias J. Tamarelle, Jeanne Ma, Bing Humphrys, Michael S. Gajer, Pawel Gwilliam, Kathleen Schaefer, Alison M. Lai, Samuel K. Terplan, Mishka Mark, Katrina S. Brotman, Rebecca M. Forney, Larry J. Bavoil, Patrik M. Ravel, Jacques mBio Research Article The mechanism(s) by which Lactobacillus-dominated cervicovaginal microbiota provide a barrier to Chlamydia trachomatis infection remain(s) unknown. Here we evaluate the impact of different Lactobacillus spp. identified via culture-independent metataxonomic analysis of C. trachomatis-infected women on C. trachomatis infection in a three-dimensional (3D) cervical epithelium model. Lactobacillus spp. that specifically produce d(−) lactic acid were associated with long-term protection against C. trachomatis infection, consistent with reduced protection associated with Lactobacillus iners, which does not produce this isoform, and with decreased epithelial cell proliferation, consistent with the observed prolonged protective effect. Transcriptomic analysis revealed that epigenetic modifications involving histone deacetylase-controlled pathways are integral to the cross talk between host and microbiota. These results highlight a fundamental mechanism whereby the cervicovaginal microbiota modulates host functions to protect against C. trachomatis infection. American Society for Microbiology 2019-08-06 /pmc/articles/PMC6692509/ /pubmed/31409678 http://dx.doi.org/10.1128/mBio.01548-19 Text en Copyright © 2019 Edwards et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Edwards, Vonetta L. Smith, Steven B. McComb, Elias J. Tamarelle, Jeanne Ma, Bing Humphrys, Michael S. Gajer, Pawel Gwilliam, Kathleen Schaefer, Alison M. Lai, Samuel K. Terplan, Mishka Mark, Katrina S. Brotman, Rebecca M. Forney, Larry J. Bavoil, Patrik M. Ravel, Jacques The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection |
title | The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection |
title_full | The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection |
title_fullStr | The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection |
title_full_unstemmed | The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection |
title_short | The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection |
title_sort | cervicovaginal microbiota-host interaction modulates chlamydia trachomatis infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692509/ https://www.ncbi.nlm.nih.gov/pubmed/31409678 http://dx.doi.org/10.1128/mBio.01548-19 |
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