학술논문

The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection
Document Type
article
Source
mBio. 10(4)
Subject
Biotechnology
Topical Microbicides
Human Genome
Sexually Transmitted Infections
Contraception/Reproduction
Genetics
Infectious Diseases
2.2 Factors relating to the physical environment
2.1 Biological and endogenous factors
Aetiology
Infection
Good Health and Well Being
Cell Movement
Cell Proliferation
Cervix Uteri
Chlamydia Infections
Chlamydia trachomatis
Female
Host Microbial Interactions
Humans
Hydrogen-Ion Concentration
Lactic Acid
Lactobacillus
Microbiota
Stereoisomerism
Transcriptome
Vagina
epigenetic
lactic acid
microbiome
proliferation
sexually transmitted infection
Microbiology
Language
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.