The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection

被引:111
作者
Edwards, Vonetta L. [1 ,2 ]
Smith, Steven B. [1 ,9 ]
McComb, Elias J. [1 ]
Tamarelle, Jeanne [3 ]
Ma, Bing [1 ,2 ]
Humphrys, Michael S. [1 ]
Gajer, Pawel [1 ,2 ]
Gwilliam, Kathleen [1 ]
Schaefer, Alison M. [4 ]
Lai, Samuel K. [4 ]
Terplan, Mishka [5 ,10 ]
Mark, Katrina S. [5 ]
Brotman, Rebecca M. [1 ,6 ]
Forney, Larry J. [7 ]
Bavoil, Patrik M. [8 ]
Ravel, Jacques [1 ,2 ]
机构
[1] Univ Maryland, Sch Med, Inst Genome Sci, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
[3] Univ Versailles St Quentin En Yvelines, Biostat Biomath Pharmacoepidemiol & Infect Dis, Inst Pasteur, INSERM, Versailles, France
[4] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27515 USA
[5] Univ Maryland, Sch Med, Dept Obstet & Gynecol, Baltimore, MD 21201 USA
[6] Univ Maryland, Sch Med, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[7] Univ Idaho, Dept Biol Sci, Moscow, ID 83843 USA
[8] Univ Maryland, Sch Dent, Dept Microbial Pathogenesis, Baltimore, MD 21201 USA
[9] PGDx, Baltimore, MD USA
[10] Virginia Commonwealth Univ, Dept Obstet & Gynecol, Richmond, VA USA
来源
MBIO | 2019年 / 10卷 / 04期
基金
美国国家卫生研究院;
关键词
Lactobacillus; epigenetic; lactic acid; microbiome; proliferation; sexually transmitted infection; VAGINAL LACTOBACILLI; BACTERIAL-VAGINOSIS; CELL-PROLIFERATION; NEISSERIA-GONORRHOEAE; HISTONE DEACETYLASES; CANCER-CELLS; CYCLIN D1; EXPRESSION; TRANSMISSION; WOMEN;
D O I
10.1128/mBio.01548-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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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页数:18
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