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Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system
Antibiotic administration, while facilitating clearance of targeted infections, also perturbs commensal microbial communities. Previous studies have all focused on the effects of short term use of antibiotics. Here, we focus on the effects of long term use of antibiotic on gut microbiota and immunit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318879/ https://www.ncbi.nlm.nih.gov/pubmed/28220870 http://dx.doi.org/10.1038/srep43035 |
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author | Guo, Yanjie Yang, Xuefei Qi, Yane Wen, Shu Liu, Yinhui Tang, Shaoying Huang, Rongsheng Tang, Li |
author_facet | Guo, Yanjie Yang, Xuefei Qi, Yane Wen, Shu Liu, Yinhui Tang, Shaoying Huang, Rongsheng Tang, Li |
author_sort | Guo, Yanjie |
collection | PubMed |
description | Antibiotic administration, while facilitating clearance of targeted infections, also perturbs commensal microbial communities. Previous studies have all focused on the effects of short term use of antibiotics. Here, we focus on the effects of long term use of antibiotic on gut microbiota and immunity. BALB/c mice received saline or different doses of ceftriaxone sodium (100, 200 and 400 mg/mL) via daily gavage for 150 days. Alterations of fecal microbiota, small intestine histopathology, body weight, spleen index, serum IgG, mucus SIgA, IFN-γ/IL-4 ratio, CD4/CD8 ratio and CD4(+)CD25(+) cells were evaluated. Long term ceftriaxone sodium administration resulted in gut microbiota dysbiosis, intestine histological lesions, growth inhibition, spleen index reducing. The immune defense ability reduced as serum IgG and mucus SIgA decreased significantly. Not only the immune defense, long term ceftriaxone administration also affected immune regulation. The IFN-γ/IL-4 and CD4/CD8 ratios increased, the CD4(+)CD25(+) cells reduced on days 30 and 60 after ceftriaxone administration. However, after 90 days of ceftriaxone administration, the IFN-γ/IL-4, CD4/CD8 ratios and CD4(+)CD25(+) cells restored, which indicated a new balance of immune regulation had been formed. Overall, these findings contribute to our understanding of long term antibiotic administration influencing gut microbiota and immunity. |
format | Online Article Text |
id | pubmed-5318879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53188792017-02-24 Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system Guo, Yanjie Yang, Xuefei Qi, Yane Wen, Shu Liu, Yinhui Tang, Shaoying Huang, Rongsheng Tang, Li Sci Rep Article Antibiotic administration, while facilitating clearance of targeted infections, also perturbs commensal microbial communities. Previous studies have all focused on the effects of short term use of antibiotics. Here, we focus on the effects of long term use of antibiotic on gut microbiota and immunity. BALB/c mice received saline or different doses of ceftriaxone sodium (100, 200 and 400 mg/mL) via daily gavage for 150 days. Alterations of fecal microbiota, small intestine histopathology, body weight, spleen index, serum IgG, mucus SIgA, IFN-γ/IL-4 ratio, CD4/CD8 ratio and CD4(+)CD25(+) cells were evaluated. Long term ceftriaxone sodium administration resulted in gut microbiota dysbiosis, intestine histological lesions, growth inhibition, spleen index reducing. The immune defense ability reduced as serum IgG and mucus SIgA decreased significantly. Not only the immune defense, long term ceftriaxone administration also affected immune regulation. The IFN-γ/IL-4 and CD4/CD8 ratios increased, the CD4(+)CD25(+) cells reduced on days 30 and 60 after ceftriaxone administration. However, after 90 days of ceftriaxone administration, the IFN-γ/IL-4, CD4/CD8 ratios and CD4(+)CD25(+) cells restored, which indicated a new balance of immune regulation had been formed. Overall, these findings contribute to our understanding of long term antibiotic administration influencing gut microbiota and immunity. Nature Publishing Group 2017-02-21 /pmc/articles/PMC5318879/ /pubmed/28220870 http://dx.doi.org/10.1038/srep43035 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Guo, Yanjie Yang, Xuefei Qi, Yane Wen, Shu Liu, Yinhui Tang, Shaoying Huang, Rongsheng Tang, Li Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
title | Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
title_full | Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
title_fullStr | Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
title_full_unstemmed | Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
title_short | Long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
title_sort | long-term use of ceftriaxone sodium induced changes in gut microbiota and immune system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318879/ https://www.ncbi.nlm.nih.gov/pubmed/28220870 http://dx.doi.org/10.1038/srep43035 |
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