Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective

Alterations in gut microbial colonization during early life have been reported in infants that later developed asthma, allergies, type 1 diabetes, as well as in inflammatory bowel disease patients, previous to disease flares. Mechanistic studies in animal models have established that microbial alter...

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Main Authors: Isabelle Laforest-Lapointe, Marie-Claire Arrieta
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.00788/full
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author Isabelle Laforest-Lapointe
Isabelle Laforest-Lapointe
Marie-Claire Arrieta
Marie-Claire Arrieta
author_facet Isabelle Laforest-Lapointe
Isabelle Laforest-Lapointe
Marie-Claire Arrieta
Marie-Claire Arrieta
author_sort Isabelle Laforest-Lapointe
collection DOAJ
description Alterations in gut microbial colonization during early life have been reported in infants that later developed asthma, allergies, type 1 diabetes, as well as in inflammatory bowel disease patients, previous to disease flares. Mechanistic studies in animal models have established that microbial alterations influence disease pathogenesis via changes in immune system maturation. Strong evidence points to the presence of a window of opportunity in early life, during which changes in gut microbial colonization can result in immune dysregulation that predisposes susceptible hosts to disease. Although the ecological patterns of microbial succession in the first year of life have been partly defined in specific human cohorts, the taxonomic and functional features, and diversity thresholds that characterize these microbial alterations are, for the most part, unknown. In this review, we summarize the most important links between the temporal mosaics of gut microbial colonization and the age-dependent immune functions that rely on them. We also highlight the importance of applying ecology theory to design studies that explore the interactions between this complex ecosystem and the host immune system. Focusing research efforts on understanding the importance of temporally structured patterns of diversity, keystone groups, and inter-kingdom microbial interactions for ecosystem functions has great potential to enable the development of biologically sound interventions aimed at maintaining and/or improving immune system development and preventing disease.
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spelling doaj.art-72fc0156db68477b9b708f078e1f67f12022-12-22T00:11:30ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-07-01810.3389/fimmu.2017.00788276727Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological PerspectiveIsabelle Laforest-Lapointe0Isabelle Laforest-Lapointe1Marie-Claire Arrieta2Marie-Claire Arrieta3Department of Physiology and Pharmacology, University of Calgary, Calgary, AB, CanadaDepartment of Pediatrics, University of Calgary, Calgary, AB, CanadaDepartment of Physiology and Pharmacology, University of Calgary, Calgary, AB, CanadaDepartment of Pediatrics, University of Calgary, Calgary, AB, CanadaAlterations in gut microbial colonization during early life have been reported in infants that later developed asthma, allergies, type 1 diabetes, as well as in inflammatory bowel disease patients, previous to disease flares. Mechanistic studies in animal models have established that microbial alterations influence disease pathogenesis via changes in immune system maturation. Strong evidence points to the presence of a window of opportunity in early life, during which changes in gut microbial colonization can result in immune dysregulation that predisposes susceptible hosts to disease. Although the ecological patterns of microbial succession in the first year of life have been partly defined in specific human cohorts, the taxonomic and functional features, and diversity thresholds that characterize these microbial alterations are, for the most part, unknown. In this review, we summarize the most important links between the temporal mosaics of gut microbial colonization and the age-dependent immune functions that rely on them. We also highlight the importance of applying ecology theory to design studies that explore the interactions between this complex ecosystem and the host immune system. Focusing research efforts on understanding the importance of temporally structured patterns of diversity, keystone groups, and inter-kingdom microbial interactions for ecosystem functions has great potential to enable the development of biologically sound interventions aimed at maintaining and/or improving immune system development and preventing disease.http://journal.frontiersin.org/article/10.3389/fimmu.2017.00788/fullmicrobiomeearly-life eventsimmune developmentmicrobial ecologydiversitykeystone taxa
spellingShingle Isabelle Laforest-Lapointe
Isabelle Laforest-Lapointe
Marie-Claire Arrieta
Marie-Claire Arrieta
Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective
Frontiers in Immunology
microbiome
early-life events
immune development
microbial ecology
diversity
keystone taxa
title Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective
title_full Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective
title_fullStr Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective
title_full_unstemmed Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective
title_short Patterns of Early-Life Gut Microbial Colonization during Human Immune Development: An Ecological Perspective
title_sort patterns of early life gut microbial colonization during human immune development an ecological perspective
topic microbiome
early-life events
immune development
microbial ecology
diversity
keystone taxa
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.00788/full
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