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Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements
The infant gut microbiota has a high abundance of antibiotic resistance genes (ARGs) compared to adults, even in the absence of antibiotic exposure. Here we study potential sources of infant gut ARGs by performing metagenomic sequencing of breast milk, as well as infant and maternal gut microbiomes....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155145/ https://www.ncbi.nlm.nih.gov/pubmed/30250208 http://dx.doi.org/10.1038/s41467-018-06393-w |
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author | Pärnänen, Katariina Karkman, Antti Hultman, Jenni Lyra, Christina Bengtsson-Palme, Johan Larsson, D. G. Joakim Rautava, Samuli Isolauri, Erika Salminen, Seppo Kumar, Himanshu Satokari, Reetta Virta, Marko |
author_facet | Pärnänen, Katariina Karkman, Antti Hultman, Jenni Lyra, Christina Bengtsson-Palme, Johan Larsson, D. G. Joakim Rautava, Samuli Isolauri, Erika Salminen, Seppo Kumar, Himanshu Satokari, Reetta Virta, Marko |
author_sort | Pärnänen, Katariina |
collection | PubMed |
description | The infant gut microbiota has a high abundance of antibiotic resistance genes (ARGs) compared to adults, even in the absence of antibiotic exposure. Here we study potential sources of infant gut ARGs by performing metagenomic sequencing of breast milk, as well as infant and maternal gut microbiomes. We find that fecal ARG and mobile genetic element (MGE) profiles of infants are more similar to those of their own mothers than to those of unrelated mothers. MGEs in mothers’ breast milk are also shared with their own infants. Termination of breastfeeding and intrapartum antibiotic prophylaxis of mothers, which have the potential to affect microbial community composition, are associated with higher abundances of specific ARGs, the composition of which is largely shaped by bacterial phylogeny in the infant gut. Our results suggest that infants inherit the legacy of past antibiotic consumption of their mothers via transmission of genes, but microbiota composition still strongly impacts the overall resistance load. |
format | Online Article Text |
id | pubmed-6155145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61551452018-09-28 Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements Pärnänen, Katariina Karkman, Antti Hultman, Jenni Lyra, Christina Bengtsson-Palme, Johan Larsson, D. G. Joakim Rautava, Samuli Isolauri, Erika Salminen, Seppo Kumar, Himanshu Satokari, Reetta Virta, Marko Nat Commun Article The infant gut microbiota has a high abundance of antibiotic resistance genes (ARGs) compared to adults, even in the absence of antibiotic exposure. Here we study potential sources of infant gut ARGs by performing metagenomic sequencing of breast milk, as well as infant and maternal gut microbiomes. We find that fecal ARG and mobile genetic element (MGE) profiles of infants are more similar to those of their own mothers than to those of unrelated mothers. MGEs in mothers’ breast milk are also shared with their own infants. Termination of breastfeeding and intrapartum antibiotic prophylaxis of mothers, which have the potential to affect microbial community composition, are associated with higher abundances of specific ARGs, the composition of which is largely shaped by bacterial phylogeny in the infant gut. Our results suggest that infants inherit the legacy of past antibiotic consumption of their mothers via transmission of genes, but microbiota composition still strongly impacts the overall resistance load. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155145/ /pubmed/30250208 http://dx.doi.org/10.1038/s41467-018-06393-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Pärnänen, Katariina Karkman, Antti Hultman, Jenni Lyra, Christina Bengtsson-Palme, Johan Larsson, D. G. Joakim Rautava, Samuli Isolauri, Erika Salminen, Seppo Kumar, Himanshu Satokari, Reetta Virta, Marko Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
title | Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
title_full | Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
title_fullStr | Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
title_full_unstemmed | Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
title_short | Maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
title_sort | maternal gut and breast milk microbiota affect infant gut antibiotic resistome and mobile genetic elements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155145/ https://www.ncbi.nlm.nih.gov/pubmed/30250208 http://dx.doi.org/10.1038/s41467-018-06393-w |
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