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The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)

Preterm infants are at a greater risk for the development of asthma and atopic disease, which can lead to lifelong negative health consequences. This may be due, in part, to alterations that occur in the gut microbiome and metabolome during their stay in the Neonatal Intensive Care Unit (NICU). To e...

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Autores principales: Bai-Tong, Shiyu S., Thoemmes, Megan S., Weldon, Kelly C., Motazavi, Diba, Kitsen, Jessica, Hansen, Shalisa, Furst, Annalee, Geng, Bob, Song, Se Jin, Gilbert, Jack A., Bode, Lars, Dorrestein, Pieter C., Knight, Rob, Leibel, Sydney A., Leibel, Sandra L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018729/
https://www.ncbi.nlm.nih.gov/pubmed/35440708
http://dx.doi.org/10.1038/s41598-022-10276-y
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author Bai-Tong, Shiyu S.
Thoemmes, Megan S.
Weldon, Kelly C.
Motazavi, Diba
Kitsen, Jessica
Hansen, Shalisa
Furst, Annalee
Geng, Bob
Song, Se Jin
Gilbert, Jack A.
Bode, Lars
Dorrestein, Pieter C.
Knight, Rob
Leibel, Sydney A.
Leibel, Sandra L.
author_facet Bai-Tong, Shiyu S.
Thoemmes, Megan S.
Weldon, Kelly C.
Motazavi, Diba
Kitsen, Jessica
Hansen, Shalisa
Furst, Annalee
Geng, Bob
Song, Se Jin
Gilbert, Jack A.
Bode, Lars
Dorrestein, Pieter C.
Knight, Rob
Leibel, Sydney A.
Leibel, Sandra L.
author_sort Bai-Tong, Shiyu S.
collection PubMed
description Preterm infants are at a greater risk for the development of asthma and atopic disease, which can lead to lifelong negative health consequences. This may be due, in part, to alterations that occur in the gut microbiome and metabolome during their stay in the Neonatal Intensive Care Unit (NICU). To explore the differential roles of family history (i.e., predisposition due to maternal asthma diagnosis) and hospital-related environmental and clinical factors that alter microbial exposures early in life, we considered a unique cohort of preterm infants born ≤ 34 weeks gestational age from two local level III NICUs, as part of the MAP (Microbiome, Atopic disease, and Prematurity) Study. From MAP participants, we chose a sub-cohort of infants whose mothers had a history of asthma and matched gestational age and sex to infants of mothers without a history of asthma diagnosis (control). We performed a prospective, paired metagenomic and metabolomic analysis of stool and milk feed samples collected at birth, 2 weeks, and 6 weeks postnatal age. Although there were clinical factors associated with shifts in the diversity and composition of stool-associated bacterial communities, maternal asthma diagnosis did not play an observable role in shaping the infant gut microbiome during the study period. There were significant differences, however, in the metabolite profile between the maternal asthma and control groups at 6 weeks postnatal age. The most notable changes occurred in the linoleic acid spectral network, which plays a role in inflammatory and immune pathways, suggesting early metabolomic changes in the gut of preterm infants born to mothers with a history of asthma. Our pilot study suggests that a history of maternal asthma alters a preterm infants’ metabolomic pathways in the gut, as early as the first 6 weeks of life.
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spelling pubmed-90187292022-04-21 The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study) Bai-Tong, Shiyu S. Thoemmes, Megan S. Weldon, Kelly C. Motazavi, Diba Kitsen, Jessica Hansen, Shalisa Furst, Annalee Geng, Bob Song, Se Jin Gilbert, Jack A. Bode, Lars Dorrestein, Pieter C. Knight, Rob Leibel, Sydney A. Leibel, Sandra L. Sci Rep Article Preterm infants are at a greater risk for the development of asthma and atopic disease, which can lead to lifelong negative health consequences. This may be due, in part, to alterations that occur in the gut microbiome and metabolome during their stay in the Neonatal Intensive Care Unit (NICU). To explore the differential roles of family history (i.e., predisposition due to maternal asthma diagnosis) and hospital-related environmental and clinical factors that alter microbial exposures early in life, we considered a unique cohort of preterm infants born ≤ 34 weeks gestational age from two local level III NICUs, as part of the MAP (Microbiome, Atopic disease, and Prematurity) Study. From MAP participants, we chose a sub-cohort of infants whose mothers had a history of asthma and matched gestational age and sex to infants of mothers without a history of asthma diagnosis (control). We performed a prospective, paired metagenomic and metabolomic analysis of stool and milk feed samples collected at birth, 2 weeks, and 6 weeks postnatal age. Although there were clinical factors associated with shifts in the diversity and composition of stool-associated bacterial communities, maternal asthma diagnosis did not play an observable role in shaping the infant gut microbiome during the study period. There were significant differences, however, in the metabolite profile between the maternal asthma and control groups at 6 weeks postnatal age. The most notable changes occurred in the linoleic acid spectral network, which plays a role in inflammatory and immune pathways, suggesting early metabolomic changes in the gut of preterm infants born to mothers with a history of asthma. Our pilot study suggests that a history of maternal asthma alters a preterm infants’ metabolomic pathways in the gut, as early as the first 6 weeks of life. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9018729/ /pubmed/35440708 http://dx.doi.org/10.1038/s41598-022-10276-y Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bai-Tong, Shiyu S.
Thoemmes, Megan S.
Weldon, Kelly C.
Motazavi, Diba
Kitsen, Jessica
Hansen, Shalisa
Furst, Annalee
Geng, Bob
Song, Se Jin
Gilbert, Jack A.
Bode, Lars
Dorrestein, Pieter C.
Knight, Rob
Leibel, Sydney A.
Leibel, Sandra L.
The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)
title The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)
title_full The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)
title_fullStr The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)
title_full_unstemmed The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)
title_short The impact of maternal asthma on the preterm infants' gut metabolome and microbiome (MAP study)
title_sort impact of maternal asthma on the preterm infants' gut metabolome and microbiome (map study)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018729/
https://www.ncbi.nlm.nih.gov/pubmed/35440708
http://dx.doi.org/10.1038/s41598-022-10276-y
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