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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
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.
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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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