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Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge

Because hospitalized preterm infants are vulnerable to infection, they receive frequent and often prolonged exposures to antibiotics. It is not known if the short-term effects of antibiotics on the preterm infant gut microbiota and resistome persist after discharge from neonatal intensive care units...

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Autores principales: Gasparrini, Andrew J., Wang, Bin, Sun, Xiaoqing, Kennedy, Elizabeth A., Hernandez-Leyva, Ariel, Ndao, I. Malick, Tarr, Phillip I., Warner, Barbara B., Dantas, Gautam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879825/
https://www.ncbi.nlm.nih.gov/pubmed/31501537
http://dx.doi.org/10.1038/s41564-019-0550-2
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author Gasparrini, Andrew J.
Wang, Bin
Sun, Xiaoqing
Kennedy, Elizabeth A.
Hernandez-Leyva, Ariel
Ndao, I. Malick
Tarr, Phillip I.
Warner, Barbara B.
Dantas, Gautam
author_facet Gasparrini, Andrew J.
Wang, Bin
Sun, Xiaoqing
Kennedy, Elizabeth A.
Hernandez-Leyva, Ariel
Ndao, I. Malick
Tarr, Phillip I.
Warner, Barbara B.
Dantas, Gautam
author_sort Gasparrini, Andrew J.
collection PubMed
description Because hospitalized preterm infants are vulnerable to infection, they receive frequent and often prolonged exposures to antibiotics. It is not known if the short-term effects of antibiotics on the preterm infant gut microbiota and resistome persist after discharge from neonatal intensive care units. Here, we use complementary metagenomic, culture based, and machine learning techniques to interrogate the gut microbiota and resistome of antibiotic-exposed preterm infants, during and after hospitalization, and compare these readouts to antibiotic-naïve healthy infants sampled synchronously. We find a persistently enriched gastrointestinal antibiotic resistome, prolonged carriage of multidrug resistant Enterobacteriaceae, and distinct antibiotic-driven patterns of microbiota and resistome assembly in extremely preterm infants who received early life antibiotics. The collateral damage of early life antibiotic treatment and hospitalization in preterm infants is long-lasting. We urge development of strategies to reduce these consequences in highly vulnerable neonatal populations.
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spelling pubmed-68798252020-03-09 Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge Gasparrini, Andrew J. Wang, Bin Sun, Xiaoqing Kennedy, Elizabeth A. Hernandez-Leyva, Ariel Ndao, I. Malick Tarr, Phillip I. Warner, Barbara B. Dantas, Gautam Nat Microbiol Article Because hospitalized preterm infants are vulnerable to infection, they receive frequent and often prolonged exposures to antibiotics. It is not known if the short-term effects of antibiotics on the preterm infant gut microbiota and resistome persist after discharge from neonatal intensive care units. Here, we use complementary metagenomic, culture based, and machine learning techniques to interrogate the gut microbiota and resistome of antibiotic-exposed preterm infants, during and after hospitalization, and compare these readouts to antibiotic-naïve healthy infants sampled synchronously. We find a persistently enriched gastrointestinal antibiotic resistome, prolonged carriage of multidrug resistant Enterobacteriaceae, and distinct antibiotic-driven patterns of microbiota and resistome assembly in extremely preterm infants who received early life antibiotics. The collateral damage of early life antibiotic treatment and hospitalization in preterm infants is long-lasting. We urge development of strategies to reduce these consequences in highly vulnerable neonatal populations. 2019-09-09 2019-12 /pmc/articles/PMC6879825/ /pubmed/31501537 http://dx.doi.org/10.1038/s41564-019-0550-2 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Gasparrini, Andrew J.
Wang, Bin
Sun, Xiaoqing
Kennedy, Elizabeth A.
Hernandez-Leyva, Ariel
Ndao, I. Malick
Tarr, Phillip I.
Warner, Barbara B.
Dantas, Gautam
Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
title Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
title_full Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
title_fullStr Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
title_full_unstemmed Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
title_short Metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
title_sort metagenomic signatures of early life hospitalization and antibiotic treatment in the infant gut microbiota and resistome persist long after discharge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879825/
https://www.ncbi.nlm.nih.gov/pubmed/31501537
http://dx.doi.org/10.1038/s41564-019-0550-2
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