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Comparative Metagenomics and Population Dynamics of the Gut Microbiota in Mother and Infant
Colonization of the gastrointestinal tract (GIT) of human infants with a suitable microbial community is essential for numerous aspects of health, but the progression of events by which this microbiota becomes established is poorly understood. Here, we investigate two previously unexplored areas of...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839348/ https://www.ncbi.nlm.nih.gov/pubmed/20333224 http://dx.doi.org/10.1093/gbe/evp057 |
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author | Vaishampayan, Parag A. Kuehl, Jennifer V. Froula, Jeffrey L. Morgan, Jenna L. Ochman, Howard Francino, M. Pilar |
author_facet | Vaishampayan, Parag A. Kuehl, Jennifer V. Froula, Jeffrey L. Morgan, Jenna L. Ochman, Howard Francino, M. Pilar |
author_sort | Vaishampayan, Parag A. |
collection | PubMed |
description | Colonization of the gastrointestinal tract (GIT) of human infants with a suitable microbial community is essential for numerous aspects of health, but the progression of events by which this microbiota becomes established is poorly understood. Here, we investigate two previously unexplored areas of microbiota development in infants: the deployment of functional capabilities at the community level and the population genetics of its most abundant genera. To assess the progression of the infant microbiota toward an adult-like state and to evaluate the contribution of maternal GIT bacteria to the infant gut, we compare the infant’s microbiota with that of the mother at 1 and 11 months after delivery. These comparisons reveal that the infant’s microbiota rapidly acquires and maintains the range of gene functions present in the mother, without replicating the phylogenetic composition of her microbiota. Microdiversity analyses for Bacteroides and Bifidobacterium, two of the main microbiota constituents, reveal that by 11 months, the phylotypes detected in the infant are distinct from those in the mother, although the maternal Bacteroides phylotypes were transiently present at 1 month of age. The configuration of genetic variants within these genera reveals populations far from equilibrium and likely to be undergoing rapid growth, consistent with recent population turnovers. Such compositional turnovers and the associated loss of maternal phylotypes should limit the potential for long-term coadaptation between specific bacterial and host genotypes. |
format | Text |
id | pubmed-2839348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28393482010-03-22 Comparative Metagenomics and Population Dynamics of the Gut Microbiota in Mother and Infant Vaishampayan, Parag A. Kuehl, Jennifer V. Froula, Jeffrey L. Morgan, Jenna L. Ochman, Howard Francino, M. Pilar Genome Biol Evol Research Articles Colonization of the gastrointestinal tract (GIT) of human infants with a suitable microbial community is essential for numerous aspects of health, but the progression of events by which this microbiota becomes established is poorly understood. Here, we investigate two previously unexplored areas of microbiota development in infants: the deployment of functional capabilities at the community level and the population genetics of its most abundant genera. To assess the progression of the infant microbiota toward an adult-like state and to evaluate the contribution of maternal GIT bacteria to the infant gut, we compare the infant’s microbiota with that of the mother at 1 and 11 months after delivery. These comparisons reveal that the infant’s microbiota rapidly acquires and maintains the range of gene functions present in the mother, without replicating the phylogenetic composition of her microbiota. Microdiversity analyses for Bacteroides and Bifidobacterium, two of the main microbiota constituents, reveal that by 11 months, the phylotypes detected in the infant are distinct from those in the mother, although the maternal Bacteroides phylotypes were transiently present at 1 month of age. The configuration of genetic variants within these genera reveals populations far from equilibrium and likely to be undergoing rapid growth, consistent with recent population turnovers. Such compositional turnovers and the associated loss of maternal phylotypes should limit the potential for long-term coadaptation between specific bacterial and host genotypes. Oxford University Press 2010 2010-01-06 /pmc/articles/PMC2839348/ /pubmed/20333224 http://dx.doi.org/10.1093/gbe/evp057 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Vaishampayan, Parag A. Kuehl, Jennifer V. Froula, Jeffrey L. Morgan, Jenna L. Ochman, Howard Francino, M. Pilar Comparative Metagenomics and Population Dynamics of the Gut Microbiota in Mother and Infant |
title | Comparative Metagenomics and Population Dynamics of the Gut
Microbiota in Mother and Infant |
title_full | Comparative Metagenomics and Population Dynamics of the Gut
Microbiota in Mother and Infant |
title_fullStr | Comparative Metagenomics and Population Dynamics of the Gut
Microbiota in Mother and Infant |
title_full_unstemmed | Comparative Metagenomics and Population Dynamics of the Gut
Microbiota in Mother and Infant |
title_short | Comparative Metagenomics and Population Dynamics of the Gut
Microbiota in Mother and Infant |
title_sort | comparative metagenomics and population dynamics of the gut
microbiota in mother and infant |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839348/ https://www.ncbi.nlm.nih.gov/pubmed/20333224 http://dx.doi.org/10.1093/gbe/evp057 |
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