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Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma

BACKGROUND: The extended 'hygiene hypothesis' suggests that the initial composition of the infant gut microbiota is a key determinant in the development of atopic disease. Several studies have demonstrated that the microbiota of allergic and non-allergic infants are different even before t...

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Autores principales: Vael, Carl, Vanheirstraeten, Liesbeth, Desager, Kristine N, Goossens, Herman
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079593/
https://www.ncbi.nlm.nih.gov/pubmed/21477358
http://dx.doi.org/10.1186/1471-2180-11-68
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author Vael, Carl
Vanheirstraeten, Liesbeth
Desager, Kristine N
Goossens, Herman
author_facet Vael, Carl
Vanheirstraeten, Liesbeth
Desager, Kristine N
Goossens, Herman
author_sort Vael, Carl
collection PubMed
description BACKGROUND: The extended 'hygiene hypothesis' suggests that the initial composition of the infant gut microbiota is a key determinant in the development of atopic disease. Several studies have demonstrated that the microbiota of allergic and non-allergic infants are different even before the development of symptoms, with a critical time window during the first 6 months of life. The aim of the study was to investigate the association between early intestinal colonisation and the development of asthma in the first 3 years of life using DGGE (denaturing gradient gel electrophoresis). METHODS: In a prospective birth cohort, 110 children were classified according to the API (Asthma Predictive Index). A positive index included wheezing during the first three years of life combined with eczema in the child in the first years of life or with a parental history of asthma. A fecal sample was taken at the age of 3 weeks and analysed with DGGE using universal and genus specific primers. RESULTS: The Asthma Predictive Index was positive in 24/110 (22%) of the children. Using universal V3 primers a band corresponding to a Clostridum coccoides XIVa species was significantly associated with a positive API. A Bacteroides fragilis subgroup band was also significantly associated with a positive API. A final DGGE model, including both bands, allowed correct classification of 73% (80/110) of the cases. CONCLUSION: Fecal colonisation at age 3 weeks with either a Bacteroides fragilis subgroup or a Clostridium coccoides subcluster XIVa species is an early indicator of possible asthma later in life. These findings need to be confirmed in a new longitudinal follow-up study.
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spelling pubmed-30795932011-04-20 Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma Vael, Carl Vanheirstraeten, Liesbeth Desager, Kristine N Goossens, Herman BMC Microbiol Research Article BACKGROUND: The extended 'hygiene hypothesis' suggests that the initial composition of the infant gut microbiota is a key determinant in the development of atopic disease. Several studies have demonstrated that the microbiota of allergic and non-allergic infants are different even before the development of symptoms, with a critical time window during the first 6 months of life. The aim of the study was to investigate the association between early intestinal colonisation and the development of asthma in the first 3 years of life using DGGE (denaturing gradient gel electrophoresis). METHODS: In a prospective birth cohort, 110 children were classified according to the API (Asthma Predictive Index). A positive index included wheezing during the first three years of life combined with eczema in the child in the first years of life or with a parental history of asthma. A fecal sample was taken at the age of 3 weeks and analysed with DGGE using universal and genus specific primers. RESULTS: The Asthma Predictive Index was positive in 24/110 (22%) of the children. Using universal V3 primers a band corresponding to a Clostridum coccoides XIVa species was significantly associated with a positive API. A Bacteroides fragilis subgroup band was also significantly associated with a positive API. A final DGGE model, including both bands, allowed correct classification of 73% (80/110) of the cases. CONCLUSION: Fecal colonisation at age 3 weeks with either a Bacteroides fragilis subgroup or a Clostridium coccoides subcluster XIVa species is an early indicator of possible asthma later in life. These findings need to be confirmed in a new longitudinal follow-up study. BioMed Central 2011-04-10 /pmc/articles/PMC3079593/ /pubmed/21477358 http://dx.doi.org/10.1186/1471-2180-11-68 Text en Copyright ©2011 Vael et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vael, Carl
Vanheirstraeten, Liesbeth
Desager, Kristine N
Goossens, Herman
Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
title Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
title_full Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
title_fullStr Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
title_full_unstemmed Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
title_short Denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
title_sort denaturing gradient gel electrophoresis of neonatal intestinal microbiota in relation to the development of asthma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079593/
https://www.ncbi.nlm.nih.gov/pubmed/21477358
http://dx.doi.org/10.1186/1471-2180-11-68
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