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Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation

Q fever is a worldwide zoonosis caused by Coxiella burnetii. Human Q fever is typically acquired through inhalation of contaminated aerosols, resulting in an initial pulmonary infection. In this study, BALB/c mice were infected with C. burnetii via an intratracheal (IT) route using a non-invasive ae...

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Autores principales: Hu, Xueyuan, Yu, Yonghui, Feng, Junxia, Fu, Mengjiao, Dai, Lupeng, Lu, Zhiyu, Luo, Wenbo, Wang, Jinglin, Zhou, Dongsheng, Xiong, Xiaolu, Wen, Bohai, Zhao, Baohua, Jiao, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894818/
https://www.ncbi.nlm.nih.gov/pubmed/31805090
http://dx.doi.org/10.1371/journal.pone.0225671
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author Hu, Xueyuan
Yu, Yonghui
Feng, Junxia
Fu, Mengjiao
Dai, Lupeng
Lu, Zhiyu
Luo, Wenbo
Wang, Jinglin
Zhou, Dongsheng
Xiong, Xiaolu
Wen, Bohai
Zhao, Baohua
Jiao, Jun
author_facet Hu, Xueyuan
Yu, Yonghui
Feng, Junxia
Fu, Mengjiao
Dai, Lupeng
Lu, Zhiyu
Luo, Wenbo
Wang, Jinglin
Zhou, Dongsheng
Xiong, Xiaolu
Wen, Bohai
Zhao, Baohua
Jiao, Jun
author_sort Hu, Xueyuan
collection PubMed
description Q fever is a worldwide zoonosis caused by Coxiella burnetii. Human Q fever is typically acquired through inhalation of contaminated aerosols, resulting in an initial pulmonary infection. In this study, BALB/c mice were infected with C. burnetii via an intratracheal (IT) route using a non-invasive aerosol pulmonary delivery device to directly place the living C. burnetii organisms into the lungs of the mice. The bacterial loads, pathological lesions, and antibody and cellular responses were analyzed and compared with those of mice infected via an intraperitoneal (IP) route. Compared with mice infected via an IP route, mice infected via an IT route exhibited a higher bacterial load and more severe pathological lesions in the heart and lungs at days 3 and 7 post-infection (pi). The levels of interferon-γ and IL-12p70 in the serum of mice infected via the IT route were significantly higher than those of mice infected via the IP route at day 3 pi. In conclusion, this murine model of acute C. burnetii infection via IT inoculation closely resembles the natural route of C. burnetii infection than that of IP injection. Thus, this newly developed model will be useful for investigating the pathogenesis and immunity of C. burnetii aerosol infection, as well as for the evaluation of therapeutic drugs and preventive vaccines of Q fever.
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spelling pubmed-68948182019-12-14 Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation Hu, Xueyuan Yu, Yonghui Feng, Junxia Fu, Mengjiao Dai, Lupeng Lu, Zhiyu Luo, Wenbo Wang, Jinglin Zhou, Dongsheng Xiong, Xiaolu Wen, Bohai Zhao, Baohua Jiao, Jun PLoS One Research Article Q fever is a worldwide zoonosis caused by Coxiella burnetii. Human Q fever is typically acquired through inhalation of contaminated aerosols, resulting in an initial pulmonary infection. In this study, BALB/c mice were infected with C. burnetii via an intratracheal (IT) route using a non-invasive aerosol pulmonary delivery device to directly place the living C. burnetii organisms into the lungs of the mice. The bacterial loads, pathological lesions, and antibody and cellular responses were analyzed and compared with those of mice infected via an intraperitoneal (IP) route. Compared with mice infected via an IP route, mice infected via an IT route exhibited a higher bacterial load and more severe pathological lesions in the heart and lungs at days 3 and 7 post-infection (pi). The levels of interferon-γ and IL-12p70 in the serum of mice infected via the IT route were significantly higher than those of mice infected via the IP route at day 3 pi. In conclusion, this murine model of acute C. burnetii infection via IT inoculation closely resembles the natural route of C. burnetii infection than that of IP injection. Thus, this newly developed model will be useful for investigating the pathogenesis and immunity of C. burnetii aerosol infection, as well as for the evaluation of therapeutic drugs and preventive vaccines of Q fever. Public Library of Science 2019-12-05 /pmc/articles/PMC6894818/ /pubmed/31805090 http://dx.doi.org/10.1371/journal.pone.0225671 Text en © 2019 Hu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hu, Xueyuan
Yu, Yonghui
Feng, Junxia
Fu, Mengjiao
Dai, Lupeng
Lu, Zhiyu
Luo, Wenbo
Wang, Jinglin
Zhou, Dongsheng
Xiong, Xiaolu
Wen, Bohai
Zhao, Baohua
Jiao, Jun
Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
title Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
title_full Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
title_fullStr Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
title_full_unstemmed Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
title_short Pathologic changes and immune responses against Coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
title_sort pathologic changes and immune responses against coxiella burnetii in mice following infection via non-invasive intratracheal inoculation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894818/
https://www.ncbi.nlm.nih.gov/pubmed/31805090
http://dx.doi.org/10.1371/journal.pone.0225671
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