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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.
Afiliação
  • Edwards VL; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Smith SB; Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • McComb EJ; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Tamarelle J; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Ma B; Biostatistics, Biomathematics, Pharmacoepidemiology and Infectious Diseases, Institut Pasteur, INSERM, Université de Versailles-Saint-Quentin-en-Yvelines, Versailles, France.
  • Humphrys MS; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Gajer P; Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Gwilliam K; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Schaefer AM; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Lai SK; Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Terplan M; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Mark KS; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Brotman RM; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Forney LJ; Department of Obstetrics and Gynecology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Bavoil PM; Department of Obstetrics and Gynecology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Ravel J; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
mBio ; 10(4)2019 08 13.
Article em En | MEDLINE | ID: mdl-31409678
ABSTRACT
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.IMPORTANCE The vaginal microbiota is believed to protect women against Chlamydia trachomatis, the etiologic agent of the most prevalent sexually transmitted infection (STI) in developed countries. The mechanism underlying this protection has remained elusive. Here, we reveal the comprehensive strategy by which the cervicovaginal microbiota modulates host functions to protect against chlamydial infection, thereby providing a novel conceptual mechanistic understanding. Major implications of this work are that (i) the impact of the vaginal microbiota on the epithelium should be considered in future studies of chlamydial infection and other STIs and (ii) a fundamental understanding of the cervicovaginal microbiota's role in protection against STIs may enable the development of novel microbiome-based therapeutic strategies to protect women from infection and improve vaginal and cervical health.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vagina / Infecções por Chlamydia / Chlamydia trachomatis / Interações entre Hospedeiro e Microrganismos Limite: Female / Humans Idioma: En Revista: MBio Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vagina / Infecções por Chlamydia / Chlamydia trachomatis / Interações entre Hospedeiro e Microrganismos Limite: Female / Humans Idioma: En Revista: MBio Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos