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Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants

The purpose of this study was to evaluate the composition and richness of bacterial communities associated with low-birthweight (LBW) infants in relation to host body site, individual, and age. Bacterial 16S rRNA genes from saliva samples, skin swabs, and stool samples collected on postnatal days 8,...

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Autores principales: Costello, Elizabeth K., Carlisle, Erica M., Bik, Elisabeth M., Morowitz, Michael J., Relman, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809564/
https://www.ncbi.nlm.nih.gov/pubmed/24169577
http://dx.doi.org/10.1128/mBio.00782-13
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author Costello, Elizabeth K.
Carlisle, Erica M.
Bik, Elisabeth M.
Morowitz, Michael J.
Relman, David A.
author_facet Costello, Elizabeth K.
Carlisle, Erica M.
Bik, Elisabeth M.
Morowitz, Michael J.
Relman, David A.
author_sort Costello, Elizabeth K.
collection PubMed
description The purpose of this study was to evaluate the composition and richness of bacterial communities associated with low-birthweight (LBW) infants in relation to host body site, individual, and age. Bacterial 16S rRNA genes from saliva samples, skin swabs, and stool samples collected on postnatal days 8, 10, 12, 15, 18, and 21 from six LBW (five premature) infants were amplified, pyrosequenced, and analyzed within a comparative framework that included analogous data from normal-birthweight (NBW) infants and healthy adults. We found that body site was the primary determinant of bacterial community composition in the LBW infants. However, site specificity depended on postnatal age: saliva and stool compositions diverged over time but were not significantly different until the babies were 15 days old. This divergence was primarily driven by progressive temporal turnover in the distal gut, which proceeded at a rate similar to that of age-matched NBW infants. Neonatal skin was the most adult-like in microbiota composition, while saliva and stool remained the least so. Compositional variation among infants was marked and depended on body site and age. Only the smallest, most premature infant received antibiotics during the study period; this heralded a coexpansion of Pseudomonas aeruginosa and a novel Mycoplasma sp. in the oral cavity of this vaginally delivered, intubated patient. We conclude that concurrent molecular surveillance of multiple body sites in LBW neonates reveals a delayed compositional differentiation of the oral cavity and distal gut microbiota and, in the case of one infant, an abundant, uncultivated oral Mycoplasma sp., recently detected in human vaginal samples.
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spelling pubmed-38095642013-10-30 Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants Costello, Elizabeth K. Carlisle, Erica M. Bik, Elisabeth M. Morowitz, Michael J. Relman, David A. mBio Research Article The purpose of this study was to evaluate the composition and richness of bacterial communities associated with low-birthweight (LBW) infants in relation to host body site, individual, and age. Bacterial 16S rRNA genes from saliva samples, skin swabs, and stool samples collected on postnatal days 8, 10, 12, 15, 18, and 21 from six LBW (five premature) infants were amplified, pyrosequenced, and analyzed within a comparative framework that included analogous data from normal-birthweight (NBW) infants and healthy adults. We found that body site was the primary determinant of bacterial community composition in the LBW infants. However, site specificity depended on postnatal age: saliva and stool compositions diverged over time but were not significantly different until the babies were 15 days old. This divergence was primarily driven by progressive temporal turnover in the distal gut, which proceeded at a rate similar to that of age-matched NBW infants. Neonatal skin was the most adult-like in microbiota composition, while saliva and stool remained the least so. Compositional variation among infants was marked and depended on body site and age. Only the smallest, most premature infant received antibiotics during the study period; this heralded a coexpansion of Pseudomonas aeruginosa and a novel Mycoplasma sp. in the oral cavity of this vaginally delivered, intubated patient. We conclude that concurrent molecular surveillance of multiple body sites in LBW neonates reveals a delayed compositional differentiation of the oral cavity and distal gut microbiota and, in the case of one infant, an abundant, uncultivated oral Mycoplasma sp., recently detected in human vaginal samples. American Society of Microbiology 2013-10-29 /pmc/articles/PMC3809564/ /pubmed/24169577 http://dx.doi.org/10.1128/mBio.00782-13 Text en Copyright © 2013 Costello et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Costello, Elizabeth K.
Carlisle, Erica M.
Bik, Elisabeth M.
Morowitz, Michael J.
Relman, David A.
Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants
title Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants
title_full Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants
title_fullStr Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants
title_full_unstemmed Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants
title_short Microbiome Assembly across Multiple Body Sites in Low-Birthweight Infants
title_sort microbiome assembly across multiple body sites in low-birthweight infants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809564/
https://www.ncbi.nlm.nih.gov/pubmed/24169577
http://dx.doi.org/10.1128/mBio.00782-13
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