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Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota

In humans, the vaginal microbiota is thought to be the first line of defense again pathogens including Chlamydia trachomatis. The guinea pig has been extensively used as a model to study chlamydial infection because it shares anatomical and physiological similarities with humans, such as a squamous...

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Autores principales: Neuendorf, Elizabeth, Gajer, Pawel, Bowlin, Anne K., Marques, Patricia X., Ma, Bing, Yang, Hongqiu, Fu, Li, Humphrys, Michael S., Forney, Larry J., Myers, Garry S.A., Bavoil, Patrik M., Rank, Roger G., Ravel, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445005/
https://www.ncbi.nlm.nih.gov/pubmed/25761873
http://dx.doi.org/10.1093/femspd/ftv019
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author Neuendorf, Elizabeth
Gajer, Pawel
Bowlin, Anne K.
Marques, Patricia X.
Ma, Bing
Yang, Hongqiu
Fu, Li
Humphrys, Michael S.
Forney, Larry J.
Myers, Garry S.A.
Bavoil, Patrik M.
Rank, Roger G.
Ravel, Jacques
author_facet Neuendorf, Elizabeth
Gajer, Pawel
Bowlin, Anne K.
Marques, Patricia X.
Ma, Bing
Yang, Hongqiu
Fu, Li
Humphrys, Michael S.
Forney, Larry J.
Myers, Garry S.A.
Bavoil, Patrik M.
Rank, Roger G.
Ravel, Jacques
author_sort Neuendorf, Elizabeth
collection PubMed
description In humans, the vaginal microbiota is thought to be the first line of defense again pathogens including Chlamydia trachomatis. The guinea pig has been extensively used as a model to study chlamydial infection because it shares anatomical and physiological similarities with humans, such as a squamous vaginal epithelium as well as some of the long-term outcomes caused by chlamydial infection. In this study, we aimed to evaluate the guinea pig-C. caviae model of genital infection as a surrogate for studying the role of the vaginal microbiota in the early steps of C. trachomatis infection in humans. We used culture-independent molecular methods to characterize the relative and absolute abundance of bacterial phylotypes in the guinea pig vaginal microbiota in animals non-infected, mock-infected or infected by C. caviae. We showed that the guinea pig and human vaginal microbiotas are of different bacterial composition and abundance. Chlamydia caviae infection had a profound effect on the absolute abundance of bacterial phylotypes but not on the composition of the guinea pig vaginal microbiota. Our findings compromise the validity of the guinea pig-C. caviae model to study the role of the vaginal microbiota during the early steps of sexually transmitted infection.
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spelling pubmed-44450052015-06-18 Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota Neuendorf, Elizabeth Gajer, Pawel Bowlin, Anne K. Marques, Patricia X. Ma, Bing Yang, Hongqiu Fu, Li Humphrys, Michael S. Forney, Larry J. Myers, Garry S.A. Bavoil, Patrik M. Rank, Roger G. Ravel, Jacques Pathog Dis Research Article In humans, the vaginal microbiota is thought to be the first line of defense again pathogens including Chlamydia trachomatis. The guinea pig has been extensively used as a model to study chlamydial infection because it shares anatomical and physiological similarities with humans, such as a squamous vaginal epithelium as well as some of the long-term outcomes caused by chlamydial infection. In this study, we aimed to evaluate the guinea pig-C. caviae model of genital infection as a surrogate for studying the role of the vaginal microbiota in the early steps of C. trachomatis infection in humans. We used culture-independent molecular methods to characterize the relative and absolute abundance of bacterial phylotypes in the guinea pig vaginal microbiota in animals non-infected, mock-infected or infected by C. caviae. We showed that the guinea pig and human vaginal microbiotas are of different bacterial composition and abundance. Chlamydia caviae infection had a profound effect on the absolute abundance of bacterial phylotypes but not on the composition of the guinea pig vaginal microbiota. Our findings compromise the validity of the guinea pig-C. caviae model to study the role of the vaginal microbiota during the early steps of sexually transmitted infection. Oxford University Press 2015-03-11 2015-06 /pmc/articles/PMC4445005/ /pubmed/25761873 http://dx.doi.org/10.1093/femspd/ftv019 Text en © FEMS 2015. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Neuendorf, Elizabeth
Gajer, Pawel
Bowlin, Anne K.
Marques, Patricia X.
Ma, Bing
Yang, Hongqiu
Fu, Li
Humphrys, Michael S.
Forney, Larry J.
Myers, Garry S.A.
Bavoil, Patrik M.
Rank, Roger G.
Ravel, Jacques
Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
title Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
title_full Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
title_fullStr Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
title_full_unstemmed Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
title_short Chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
title_sort chlamydia caviae infection alters abundance but not composition of the guinea pig vaginal microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445005/
https://www.ncbi.nlm.nih.gov/pubmed/25761873
http://dx.doi.org/10.1093/femspd/ftv019
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