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Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota
Antibiotics can promote growth in livestock (antimicrobial growth promoters, AGPs), however lack of knowledge regarding mechanisms has hampered the development of effective non-antibiotic alternatives. Antibiotics affect eukaryotic cells at therapeutic concentrations, yet effects of AGPs on host phy...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144068/ https://www.ncbi.nlm.nih.gov/pubmed/27929072 http://dx.doi.org/10.1038/srep38377 |
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author | Brown, Kirsty Zaytsoff, Sarah J. M. Uwiera, Richard R. E. Inglis, G. Douglas |
author_facet | Brown, Kirsty Zaytsoff, Sarah J. M. Uwiera, Richard R. E. Inglis, G. Douglas |
author_sort | Brown, Kirsty |
collection | PubMed |
description | Antibiotics can promote growth in livestock (antimicrobial growth promoters, AGPs), however lack of knowledge regarding mechanisms has hampered the development of effective non-antibiotic alternatives. Antibiotics affect eukaryotic cells at therapeutic concentrations, yet effects of AGPs on host physiology are relatively understudied, partially due to the complexity of host-microorganism interactions within the gastrointestinal tract. To determine the direct effects of AGPs on the host, we generated Altered Schaedler Flora (ASF) mice, and administered chlortetracycline (CTC) and tylosin phosphate (TYL) in feed. Mice were challenged with Citrobacter rodentium to determine how AGPs alter host responses to physiological stress. Although CTC and TYL had inconsistent effects on the ASF taxa, AGPs protected mice from weight loss following C. rodentium inoculation. Mice treated with either CTC or TYL had lower expression of βd1 and Il17a in the intestine and had a robust induction of Il17a and Il10. Furthermore, AGP administration resulted in a lower hepatic expression of acute phase proteins (Saa1, Hp, and Cp) in liver tissue, and ameliorated C. rodentium-induced reductions in the expression of genes involved in lipogenesis (Hmgcl and Fabp1). Collectively, this indicates that AGPs directly affect host physiology, and highlights important considerations in the development of non-antibiotic alternatives. |
format | Online Article Text |
id | pubmed-5144068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51440682016-12-16 Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota Brown, Kirsty Zaytsoff, Sarah J. M. Uwiera, Richard R. E. Inglis, G. Douglas Sci Rep Article Antibiotics can promote growth in livestock (antimicrobial growth promoters, AGPs), however lack of knowledge regarding mechanisms has hampered the development of effective non-antibiotic alternatives. Antibiotics affect eukaryotic cells at therapeutic concentrations, yet effects of AGPs on host physiology are relatively understudied, partially due to the complexity of host-microorganism interactions within the gastrointestinal tract. To determine the direct effects of AGPs on the host, we generated Altered Schaedler Flora (ASF) mice, and administered chlortetracycline (CTC) and tylosin phosphate (TYL) in feed. Mice were challenged with Citrobacter rodentium to determine how AGPs alter host responses to physiological stress. Although CTC and TYL had inconsistent effects on the ASF taxa, AGPs protected mice from weight loss following C. rodentium inoculation. Mice treated with either CTC or TYL had lower expression of βd1 and Il17a in the intestine and had a robust induction of Il17a and Il10. Furthermore, AGP administration resulted in a lower hepatic expression of acute phase proteins (Saa1, Hp, and Cp) in liver tissue, and ameliorated C. rodentium-induced reductions in the expression of genes involved in lipogenesis (Hmgcl and Fabp1). Collectively, this indicates that AGPs directly affect host physiology, and highlights important considerations in the development of non-antibiotic alternatives. Nature Publishing Group 2016-12-08 /pmc/articles/PMC5144068/ /pubmed/27929072 http://dx.doi.org/10.1038/srep38377 Text en Copyright © 2016, 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 Brown, Kirsty Zaytsoff, Sarah J. M. Uwiera, Richard R. E. Inglis, G. Douglas Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
title | Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
title_full | Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
title_fullStr | Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
title_full_unstemmed | Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
title_short | Antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
title_sort | antimicrobial growth promoters modulate host responses in mice with a defined intestinal microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144068/ https://www.ncbi.nlm.nih.gov/pubmed/27929072 http://dx.doi.org/10.1038/srep38377 |
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