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The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge

BACKGROUND: Preterm birth is associated with the development of acute and chronic disease, potentially, through the disruption of normal gut microbiome development. Probiotics may correct for microbial imbalances and mitigate disease risk. Here, we used amplicon sequencing to characterise the gut mi...

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Autores principales: Westaway, Jacob A. F., Huerlimann, Roger, Kandasamy, Yoga, Miller, Catherine M., Norton, Robert, Staunton, Kyran M., Watson, David, Rudd, Donna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411061/
https://www.ncbi.nlm.nih.gov/pubmed/34621029
http://dx.doi.org/10.1038/s41390-021-01738-6
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author Westaway, Jacob A. F.
Huerlimann, Roger
Kandasamy, Yoga
Miller, Catherine M.
Norton, Robert
Staunton, Kyran M.
Watson, David
Rudd, Donna
author_facet Westaway, Jacob A. F.
Huerlimann, Roger
Kandasamy, Yoga
Miller, Catherine M.
Norton, Robert
Staunton, Kyran M.
Watson, David
Rudd, Donna
author_sort Westaway, Jacob A. F.
collection PubMed
description BACKGROUND: Preterm birth is associated with the development of acute and chronic disease, potentially, through the disruption of normal gut microbiome development. Probiotics may correct for microbial imbalances and mitigate disease risk. Here, we used amplicon sequencing to characterise the gut microbiome of probiotic-treated premature infants. We aimed to identify and understand variation in bacterial gut flora from admission to discharge and in association with clinical variables. METHODS: Infants born <32 weeks gestation and <1500 g, and who received probiotic treatment, were recruited in North Queensland Australia. Meconium and faecal samples were collected at admission and discharge. All samples underwent 16S rRNA short amplicon sequencing, and subsequently, a combination of univariate and multivariate analyses. RESULTS: 71 admission and 63 discharge samples were collected. Univariate analyses showed significant changes in the gut flora from admission to discharge. Mixed-effects modelling showed significantly lower alpha diversity in infants diagnosed with either sepsis or retinopathy of prematurity (ROP) and those fed formula. In addition, chorioamnionitis, preeclampsia, sepsis, necrotising enterocolitis and ROP were also all associated with the differential abundance of several taxa. CONCLUSIONS: The lower microbial diversity seen in infants with diagnosed disorders or formula-fed, as well as differing abundances of several taxa across multiple variables, highlights the role of the microbiome in the development of health and disease. This study supports the need for promoting healthy microbiome development in preterm neonates. IMPACT: Low diversity and differing taxonomic abundances in preterm gut microbiota demonstrated in formula-fed infants and those identified with postnatal conditions, as well as differences in taxonomy associated with preeclampsia and chorioamnionitis, reinforcing the association of the microbiome composition changes due to maternal and infant disease. The largest study exploring an association between the preterm infant microbiome and ROP. A novel association between the preterm infant gut microbiome and preeclampsia in a unique cohort of very-premature probiotic-supplemented infants.
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spelling pubmed-94110612022-08-27 The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge Westaway, Jacob A. F. Huerlimann, Roger Kandasamy, Yoga Miller, Catherine M. Norton, Robert Staunton, Kyran M. Watson, David Rudd, Donna Pediatr Res Clinical Research Article BACKGROUND: Preterm birth is associated with the development of acute and chronic disease, potentially, through the disruption of normal gut microbiome development. Probiotics may correct for microbial imbalances and mitigate disease risk. Here, we used amplicon sequencing to characterise the gut microbiome of probiotic-treated premature infants. We aimed to identify and understand variation in bacterial gut flora from admission to discharge and in association with clinical variables. METHODS: Infants born <32 weeks gestation and <1500 g, and who received probiotic treatment, were recruited in North Queensland Australia. Meconium and faecal samples were collected at admission and discharge. All samples underwent 16S rRNA short amplicon sequencing, and subsequently, a combination of univariate and multivariate analyses. RESULTS: 71 admission and 63 discharge samples were collected. Univariate analyses showed significant changes in the gut flora from admission to discharge. Mixed-effects modelling showed significantly lower alpha diversity in infants diagnosed with either sepsis or retinopathy of prematurity (ROP) and those fed formula. In addition, chorioamnionitis, preeclampsia, sepsis, necrotising enterocolitis and ROP were also all associated with the differential abundance of several taxa. CONCLUSIONS: The lower microbial diversity seen in infants with diagnosed disorders or formula-fed, as well as differing abundances of several taxa across multiple variables, highlights the role of the microbiome in the development of health and disease. This study supports the need for promoting healthy microbiome development in preterm neonates. IMPACT: Low diversity and differing taxonomic abundances in preterm gut microbiota demonstrated in formula-fed infants and those identified with postnatal conditions, as well as differences in taxonomy associated with preeclampsia and chorioamnionitis, reinforcing the association of the microbiome composition changes due to maternal and infant disease. The largest study exploring an association between the preterm infant microbiome and ROP. A novel association between the preterm infant gut microbiome and preeclampsia in a unique cohort of very-premature probiotic-supplemented infants. Nature Publishing Group US 2021-10-07 2022 /pmc/articles/PMC9411061/ /pubmed/34621029 http://dx.doi.org/10.1038/s41390-021-01738-6 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Research Article
Westaway, Jacob A. F.
Huerlimann, Roger
Kandasamy, Yoga
Miller, Catherine M.
Norton, Robert
Staunton, Kyran M.
Watson, David
Rudd, Donna
The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
title The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
title_full The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
title_fullStr The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
title_full_unstemmed The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
title_short The bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
title_sort bacterial gut microbiome of probiotic-treated very-preterm infants: changes from admission to discharge
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411061/
https://www.ncbi.nlm.nih.gov/pubmed/34621029
http://dx.doi.org/10.1038/s41390-021-01738-6
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