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Characterization of Treponema pallidum Dissemination in C57BL/6 Mice

The spirochetal pathogen Treponema pallidum causes 5 million new cases of venereal syphilis worldwide each year. One major obstacle to syphilis prevention and treatment is the lack of suitable experimental animal models to study its pathogenesis. Accordingly, in this study, we further evaluated the...

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Autores principales: Lu, Simin, Zheng, Kang, Wang, Jianye, Xu, Man, Xie, Yafeng, Yuan, Shuai, Wang, Chuan, Wu, Yimou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819853/
https://www.ncbi.nlm.nih.gov/pubmed/33488577
http://dx.doi.org/10.3389/fimmu.2020.577129
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author Lu, Simin
Zheng, Kang
Wang, Jianye
Xu, Man
Xie, Yafeng
Yuan, Shuai
Wang, Chuan
Wu, Yimou
author_facet Lu, Simin
Zheng, Kang
Wang, Jianye
Xu, Man
Xie, Yafeng
Yuan, Shuai
Wang, Chuan
Wu, Yimou
author_sort Lu, Simin
collection PubMed
description The spirochetal pathogen Treponema pallidum causes 5 million new cases of venereal syphilis worldwide each year. One major obstacle to syphilis prevention and treatment is the lack of suitable experimental animal models to study its pathogenesis. Accordingly, in this study, we further evaluated the responses of mice to Treponema pallidum. Quantitative polymerase chain reaction showed that Treponema pallidum could colonize the heart, liver, spleen, kidneys, and testicles of C57BL/6 mice, and the organism may be able to rapidly penetrate the blood-brain barrier in mice by 24 h after infection. In subsequent rabbit infectivity tests, we observed evident signs of the microorganism in the mouse lymph node suspension. After infection, bacterial loads were higher in the tissues than in the blood of C57BL/6 mice. Moreover, a significant Th1 immune response was recorded by cytokine assays. Flow cytometric analysis suggested an obvious increase in the proportion of CD3(+) T and CD4(+) T cells in the spleen cells in the infected mice. Thus, improving our understanding of the response of C57BL/6 mice for Treponema pallidum will help to comprehensive elucidate the pathogenic mechanisms of this bacterium and lay the foundation for the development of a new research model of Treponema pallidum.
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spelling pubmed-78198532021-01-23 Characterization of Treponema pallidum Dissemination in C57BL/6 Mice Lu, Simin Zheng, Kang Wang, Jianye Xu, Man Xie, Yafeng Yuan, Shuai Wang, Chuan Wu, Yimou Front Immunol Immunology The spirochetal pathogen Treponema pallidum causes 5 million new cases of venereal syphilis worldwide each year. One major obstacle to syphilis prevention and treatment is the lack of suitable experimental animal models to study its pathogenesis. Accordingly, in this study, we further evaluated the responses of mice to Treponema pallidum. Quantitative polymerase chain reaction showed that Treponema pallidum could colonize the heart, liver, spleen, kidneys, and testicles of C57BL/6 mice, and the organism may be able to rapidly penetrate the blood-brain barrier in mice by 24 h after infection. In subsequent rabbit infectivity tests, we observed evident signs of the microorganism in the mouse lymph node suspension. After infection, bacterial loads were higher in the tissues than in the blood of C57BL/6 mice. Moreover, a significant Th1 immune response was recorded by cytokine assays. Flow cytometric analysis suggested an obvious increase in the proportion of CD3(+) T and CD4(+) T cells in the spleen cells in the infected mice. Thus, improving our understanding of the response of C57BL/6 mice for Treponema pallidum will help to comprehensive elucidate the pathogenic mechanisms of this bacterium and lay the foundation for the development of a new research model of Treponema pallidum. Frontiers Media S.A. 2021-01-08 /pmc/articles/PMC7819853/ /pubmed/33488577 http://dx.doi.org/10.3389/fimmu.2020.577129 Text en Copyright © 2021 Lu, Zheng, Wang, Xu, Xie, Yuan, Wang and Wu http://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 Immunology
Lu, Simin
Zheng, Kang
Wang, Jianye
Xu, Man
Xie, Yafeng
Yuan, Shuai
Wang, Chuan
Wu, Yimou
Characterization of Treponema pallidum Dissemination in C57BL/6 Mice
title Characterization of Treponema pallidum Dissemination in C57BL/6 Mice
title_full Characterization of Treponema pallidum Dissemination in C57BL/6 Mice
title_fullStr Characterization of Treponema pallidum Dissemination in C57BL/6 Mice
title_full_unstemmed Characterization of Treponema pallidum Dissemination in C57BL/6 Mice
title_short Characterization of Treponema pallidum Dissemination in C57BL/6 Mice
title_sort characterization of treponema pallidum dissemination in c57bl/6 mice
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819853/
https://www.ncbi.nlm.nih.gov/pubmed/33488577
http://dx.doi.org/10.3389/fimmu.2020.577129
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