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Maturational patterns of the infant gut mycobiome are associated with early-life body mass index

Unlike the bacterial microbiome, the role of early-life gut fungi in host metabolism and childhood obesity development remains poorly characterized. To address this, we investigate the relationship between the gut mycobiome of 100 infants from the Canadian Healthy Infant Longitudinal Development (CH...

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Autores principales: Gutierrez, Mackenzie W., Mercer, Emily M., Moossavi, Shirin, Laforest-Lapointe, Isabelle, Reyna, Myrtha E., Becker, Allan B., Simons, Elinor, Mandhane, Piush J., Turvey, Stuart E., Moraes, Theo J., Sears, Malcolm R., Subbarao, Padmaja, Azad, Meghan B., Arrieta, Marie-Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975311/
https://www.ncbi.nlm.nih.gov/pubmed/36736319
http://dx.doi.org/10.1016/j.xcrm.2023.100928
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author Gutierrez, Mackenzie W.
Mercer, Emily M.
Moossavi, Shirin
Laforest-Lapointe, Isabelle
Reyna, Myrtha E.
Becker, Allan B.
Simons, Elinor
Mandhane, Piush J.
Turvey, Stuart E.
Moraes, Theo J.
Sears, Malcolm R.
Subbarao, Padmaja
Azad, Meghan B.
Arrieta, Marie-Claire
author_facet Gutierrez, Mackenzie W.
Mercer, Emily M.
Moossavi, Shirin
Laforest-Lapointe, Isabelle
Reyna, Myrtha E.
Becker, Allan B.
Simons, Elinor
Mandhane, Piush J.
Turvey, Stuart E.
Moraes, Theo J.
Sears, Malcolm R.
Subbarao, Padmaja
Azad, Meghan B.
Arrieta, Marie-Claire
author_sort Gutierrez, Mackenzie W.
collection PubMed
description Unlike the bacterial microbiome, the role of early-life gut fungi in host metabolism and childhood obesity development remains poorly characterized. To address this, we investigate the relationship between the gut mycobiome of 100 infants from the Canadian Healthy Infant Longitudinal Development (CHILD) Cohort Study and body mass index Z scores (BMIz) in the first 5 years of life. An increase in fungal richness during the first year of life is linked to parental and infant BMI. The relationship between richness pattern and early-life BMIz is modified by maternal BMI, maternal diet, infant antibiotic exposure, and bacterial beta diversity. Further, the abundances of Saccharomyces, Rhodotorula, and Malassezia are differentially associated with early-life BMIz. Using structural equation modeling, we determine that the mycobiome’s contribution to BMIz is likely mediated by the bacterial microbiome. This demonstrates that mycobiome maturation and infant growth trajectories are distinctly linked, advocating for inclusion of fungi in larger pediatric microbiome studies.
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spelling pubmed-99753112023-03-02 Maturational patterns of the infant gut mycobiome are associated with early-life body mass index Gutierrez, Mackenzie W. Mercer, Emily M. Moossavi, Shirin Laforest-Lapointe, Isabelle Reyna, Myrtha E. Becker, Allan B. Simons, Elinor Mandhane, Piush J. Turvey, Stuart E. Moraes, Theo J. Sears, Malcolm R. Subbarao, Padmaja Azad, Meghan B. Arrieta, Marie-Claire Cell Rep Med Report Unlike the bacterial microbiome, the role of early-life gut fungi in host metabolism and childhood obesity development remains poorly characterized. To address this, we investigate the relationship between the gut mycobiome of 100 infants from the Canadian Healthy Infant Longitudinal Development (CHILD) Cohort Study and body mass index Z scores (BMIz) in the first 5 years of life. An increase in fungal richness during the first year of life is linked to parental and infant BMI. The relationship between richness pattern and early-life BMIz is modified by maternal BMI, maternal diet, infant antibiotic exposure, and bacterial beta diversity. Further, the abundances of Saccharomyces, Rhodotorula, and Malassezia are differentially associated with early-life BMIz. Using structural equation modeling, we determine that the mycobiome’s contribution to BMIz is likely mediated by the bacterial microbiome. This demonstrates that mycobiome maturation and infant growth trajectories are distinctly linked, advocating for inclusion of fungi in larger pediatric microbiome studies. Elsevier 2023-02-02 /pmc/articles/PMC9975311/ /pubmed/36736319 http://dx.doi.org/10.1016/j.xcrm.2023.100928 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Report
Gutierrez, Mackenzie W.
Mercer, Emily M.
Moossavi, Shirin
Laforest-Lapointe, Isabelle
Reyna, Myrtha E.
Becker, Allan B.
Simons, Elinor
Mandhane, Piush J.
Turvey, Stuart E.
Moraes, Theo J.
Sears, Malcolm R.
Subbarao, Padmaja
Azad, Meghan B.
Arrieta, Marie-Claire
Maturational patterns of the infant gut mycobiome are associated with early-life body mass index
title Maturational patterns of the infant gut mycobiome are associated with early-life body mass index
title_full Maturational patterns of the infant gut mycobiome are associated with early-life body mass index
title_fullStr Maturational patterns of the infant gut mycobiome are associated with early-life body mass index
title_full_unstemmed Maturational patterns of the infant gut mycobiome are associated with early-life body mass index
title_short Maturational patterns of the infant gut mycobiome are associated with early-life body mass index
title_sort maturational patterns of the infant gut mycobiome are associated with early-life body mass index
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975311/
https://www.ncbi.nlm.nih.gov/pubmed/36736319
http://dx.doi.org/10.1016/j.xcrm.2023.100928
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