Cargando…

Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract

Chlamydia trachomatis is one of the most common sexually infections that cause infertility, and its genital infection induces tubal adhesion and hydrosalpinx. Intravaginal Chlamydia muridarum infection in mice can induce hydrosalpinx in the upper genital tract and it has been used for studying C. tr...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Qi, Zhang, Tianyuan, Wang, Luying, Ma, Jingyue, Sun, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133527/
https://www.ncbi.nlm.nih.gov/pubmed/37125189
http://dx.doi.org/10.3389/fmicb.2023.1142283
_version_ 1785031587185819648
author Tian, Qi
Zhang, Tianyuan
Wang, Luying
Ma, Jingyue
Sun, Xin
author_facet Tian, Qi
Zhang, Tianyuan
Wang, Luying
Ma, Jingyue
Sun, Xin
author_sort Tian, Qi
collection PubMed
description Chlamydia trachomatis is one of the most common sexually infections that cause infertility, and its genital infection induces tubal adhesion and hydrosalpinx. Intravaginal Chlamydia muridarum infection in mice can induce hydrosalpinx in the upper genital tract and it has been used for studying C. trachomatis pathogenicity. DBA2/J strain mice were known to be resistant to the chlamydial induction of hydrosalpinx. In this study, we took advantage of this feature of DBA2/J mice to evaluate the role of antibiotic induced dysbiosis in chlamydial pathogenicity. Antibiotics (vancomycin and gentamicin) were orally administrated to induce dysbiosis in the gut of DBA2/J mice. The mice with or without antibiotic treatment were evaluated for gut and genital dysbiosis and then intravaginally challenged by C. muridarum. Chlamydial burden was tested and genital pathologies were evaluated. We found that oral antibiotics significantly enhanced chlamydial induction of genital hydrosalpinx. And the antibiotic treatment induced severe dysbiosis in the GI tract, including significantly reduced fecal DNA and increased ratios of firmicutes over bacteroidetes. The oral antibiotic did not alter chlamydial infection or microbiota in the mouse genital tracts. Our study showed that the oral antibiotics-enhanced hydrosalpinx correlated with dysbiosis in gut, providing the evidence for associating gut microbiome with chlamydial genital pathogenicity.
format Online
Article
Text
id pubmed-10133527
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-101335272023-04-28 Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract Tian, Qi Zhang, Tianyuan Wang, Luying Ma, Jingyue Sun, Xin Front Microbiol Microbiology Chlamydia trachomatis is one of the most common sexually infections that cause infertility, and its genital infection induces tubal adhesion and hydrosalpinx. Intravaginal Chlamydia muridarum infection in mice can induce hydrosalpinx in the upper genital tract and it has been used for studying C. trachomatis pathogenicity. DBA2/J strain mice were known to be resistant to the chlamydial induction of hydrosalpinx. In this study, we took advantage of this feature of DBA2/J mice to evaluate the role of antibiotic induced dysbiosis in chlamydial pathogenicity. Antibiotics (vancomycin and gentamicin) were orally administrated to induce dysbiosis in the gut of DBA2/J mice. The mice with or without antibiotic treatment were evaluated for gut and genital dysbiosis and then intravaginally challenged by C. muridarum. Chlamydial burden was tested and genital pathologies were evaluated. We found that oral antibiotics significantly enhanced chlamydial induction of genital hydrosalpinx. And the antibiotic treatment induced severe dysbiosis in the GI tract, including significantly reduced fecal DNA and increased ratios of firmicutes over bacteroidetes. The oral antibiotic did not alter chlamydial infection or microbiota in the mouse genital tracts. Our study showed that the oral antibiotics-enhanced hydrosalpinx correlated with dysbiosis in gut, providing the evidence for associating gut microbiome with chlamydial genital pathogenicity. Frontiers Media S.A. 2023-04-13 /pmc/articles/PMC10133527/ /pubmed/37125189 http://dx.doi.org/10.3389/fmicb.2023.1142283 Text en Copyright © 2023 Tian, Zhang, Wang, Ma and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Tian, Qi
Zhang, Tianyuan
Wang, Luying
Ma, Jingyue
Sun, Xin
Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
title Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
title_full Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
title_fullStr Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
title_full_unstemmed Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
title_short Gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
title_sort gut dysbiosis contributes to chlamydial induction of hydrosalpinx in the upper genital tract
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133527/
https://www.ncbi.nlm.nih.gov/pubmed/37125189
http://dx.doi.org/10.3389/fmicb.2023.1142283
work_keys_str_mv AT tianqi gutdysbiosiscontributestochlamydialinductionofhydrosalpinxintheuppergenitaltract
AT zhangtianyuan gutdysbiosiscontributestochlamydialinductionofhydrosalpinxintheuppergenitaltract
AT wangluying gutdysbiosiscontributestochlamydialinductionofhydrosalpinxintheuppergenitaltract
AT majingyue gutdysbiosiscontributestochlamydialinductionofhydrosalpinxintheuppergenitaltract
AT sunxin gutdysbiosiscontributestochlamydialinductionofhydrosalpinxintheuppergenitaltract