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Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats
Alteration of gut microbial colonization process may influence susceptibility of the newborn/infant to infectious and chronic disease. Infectious disease risk leads to widespread use of non-prescription antimicrobials in household products such as Triclocarban (TCC), an antimicrobial compound in per...
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/PMC5028839/ https://www.ncbi.nlm.nih.gov/pubmed/27646684 http://dx.doi.org/10.1038/srep33430 |
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author | Kennedy, Rebekah C. Fling, Russell R. Robeson, Michael S. Saxton, Arnold M. Donnell, Robert L. Darcy, John L. Bemis, David A. Liu, Jiang Zhao, Ling Chen, Jiangang |
author_facet | Kennedy, Rebekah C. Fling, Russell R. Robeson, Michael S. Saxton, Arnold M. Donnell, Robert L. Darcy, John L. Bemis, David A. Liu, Jiang Zhao, Ling Chen, Jiangang |
author_sort | Kennedy, Rebekah C. |
collection | PubMed |
description | Alteration of gut microbial colonization process may influence susceptibility of the newborn/infant to infectious and chronic disease. Infectious disease risk leads to widespread use of non-prescription antimicrobials in household products such as Triclocarban (TCC), an antimicrobial compound in personal care products. TCC concentrates in and is transferred through the milk to suckling offspring. TCC exposure during gestation and lactation significantly reduced phylogenetic diversity (PD) among exposed dams and neonates. Among dams using weighted UniFrac distances, TCC induced significant dysbiosis of gut microbiota by gestational day (GD) 18, a trend that continued after delivery. Similarly, an overall restructuring of gut microbiota occurred in neonates. By postnatal day (PND) 12, communities separated based on exposure status and became significantly different at PND 16. The ability of TCC to drive microbial dysbiosis warrants future investigation to evaluate the safety of non-prescription antimicrobial use, including TCC, during critical exposure windows. |
format | Online Article Text |
id | pubmed-5028839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50288392016-09-26 Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats Kennedy, Rebekah C. Fling, Russell R. Robeson, Michael S. Saxton, Arnold M. Donnell, Robert L. Darcy, John L. Bemis, David A. Liu, Jiang Zhao, Ling Chen, Jiangang Sci Rep Article Alteration of gut microbial colonization process may influence susceptibility of the newborn/infant to infectious and chronic disease. Infectious disease risk leads to widespread use of non-prescription antimicrobials in household products such as Triclocarban (TCC), an antimicrobial compound in personal care products. TCC concentrates in and is transferred through the milk to suckling offspring. TCC exposure during gestation and lactation significantly reduced phylogenetic diversity (PD) among exposed dams and neonates. Among dams using weighted UniFrac distances, TCC induced significant dysbiosis of gut microbiota by gestational day (GD) 18, a trend that continued after delivery. Similarly, an overall restructuring of gut microbiota occurred in neonates. By postnatal day (PND) 12, communities separated based on exposure status and became significantly different at PND 16. The ability of TCC to drive microbial dysbiosis warrants future investigation to evaluate the safety of non-prescription antimicrobial use, including TCC, during critical exposure windows. Nature Publishing Group 2016-09-20 /pmc/articles/PMC5028839/ /pubmed/27646684 http://dx.doi.org/10.1038/srep33430 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 Kennedy, Rebekah C. Fling, Russell R. Robeson, Michael S. Saxton, Arnold M. Donnell, Robert L. Darcy, John L. Bemis, David A. Liu, Jiang Zhao, Ling Chen, Jiangang Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats |
title | Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats |
title_full | Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats |
title_fullStr | Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats |
title_full_unstemmed | Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats |
title_short | Temporal Development of Gut Microbiota in Triclocarban Exposed Pregnant and Neonatal Rats |
title_sort | temporal development of gut microbiota in triclocarban exposed pregnant and neonatal rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028839/ https://www.ncbi.nlm.nih.gov/pubmed/27646684 http://dx.doi.org/10.1038/srep33430 |
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