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Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics

The infant gut microbiome consists of a complex and diverse microbial community. Comprehensive taxonomic and metabolic functional knowledge about microbial communities supports medical and biological applications, such as fecal diagnostics. Among the omics approaches available for the investigation...

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Autores principales: Kingkaw, Amornthep, Nakphaichit, Massalin, Suratannon, Narissara, Nitisinprasert, Sunee, Wongoutong, Chantha, Chatchatee, Pantipa, Krobthong, Sucheewin, Charoenlappanit, Sawanya, Roytrakul, Sittiruk, Vongsangnak, Wanwipa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521340/
https://www.ncbi.nlm.nih.gov/pubmed/33033661
http://dx.doi.org/10.7717/peerj.9988
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author Kingkaw, Amornthep
Nakphaichit, Massalin
Suratannon, Narissara
Nitisinprasert, Sunee
Wongoutong, Chantha
Chatchatee, Pantipa
Krobthong, Sucheewin
Charoenlappanit, Sawanya
Roytrakul, Sittiruk
Vongsangnak, Wanwipa
author_facet Kingkaw, Amornthep
Nakphaichit, Massalin
Suratannon, Narissara
Nitisinprasert, Sunee
Wongoutong, Chantha
Chatchatee, Pantipa
Krobthong, Sucheewin
Charoenlappanit, Sawanya
Roytrakul, Sittiruk
Vongsangnak, Wanwipa
author_sort Kingkaw, Amornthep
collection PubMed
description The infant gut microbiome consists of a complex and diverse microbial community. Comprehensive taxonomic and metabolic functional knowledge about microbial communities supports medical and biological applications, such as fecal diagnostics. Among the omics approaches available for the investigation of microbial communities, metaproteomics-based analysis is a very powerful approach; under this method, the activity of microbial communities is explored by investigating protein expression within a sample. Through use of metaproteomics, this study aimed to investigate the microbial community composition of the infant gut to identify different key proteins playing metabolic functional roles in the microbiome of healthy infants and infants with atopic dermatitis in a Thai population-based birth cohort. Here, 18 fecal samples were analyzed by liquid chromatography-tandem mass spectrometry to conduct taxonomic, functional, and pathway-based protein annotation. Accordingly, 49,973 annotated proteins out of 68,232 total proteins were investigated in gut microbiome samples and compared between the healthy and atopic dermatitis groups. Through differentially expressed proteins (DEPs) analysis, 130 significant DEPs were identified between the healthy and atopic dermatitis groups. Among these DEPs, eight significant proteins were uniquely expressed in the atopic dermatitis group. For instance, triosephosphate isomerase (TPI) in Bifidobacteriaceae in the genus Alloscardovia and demethylmenaquinone methyltransferase (DMM) in Bacteroides were shown to potentially play metabolic functional roles related to disease. PPI network analysis revealed seven reporter proteins showing metabolic alterations between the healthy and disease groups associated with the biosynthesis of ubiquinone and other quinones as well as the energy supply. This study serves as a scaffold for microbial community-wide metabolic functional studies of the infant gut microbiome in relation to allergic disease.
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spelling pubmed-75213402020-10-07 Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics Kingkaw, Amornthep Nakphaichit, Massalin Suratannon, Narissara Nitisinprasert, Sunee Wongoutong, Chantha Chatchatee, Pantipa Krobthong, Sucheewin Charoenlappanit, Sawanya Roytrakul, Sittiruk Vongsangnak, Wanwipa PeerJ Bioinformatics The infant gut microbiome consists of a complex and diverse microbial community. Comprehensive taxonomic and metabolic functional knowledge about microbial communities supports medical and biological applications, such as fecal diagnostics. Among the omics approaches available for the investigation of microbial communities, metaproteomics-based analysis is a very powerful approach; under this method, the activity of microbial communities is explored by investigating protein expression within a sample. Through use of metaproteomics, this study aimed to investigate the microbial community composition of the infant gut to identify different key proteins playing metabolic functional roles in the microbiome of healthy infants and infants with atopic dermatitis in a Thai population-based birth cohort. Here, 18 fecal samples were analyzed by liquid chromatography-tandem mass spectrometry to conduct taxonomic, functional, and pathway-based protein annotation. Accordingly, 49,973 annotated proteins out of 68,232 total proteins were investigated in gut microbiome samples and compared between the healthy and atopic dermatitis groups. Through differentially expressed proteins (DEPs) analysis, 130 significant DEPs were identified between the healthy and atopic dermatitis groups. Among these DEPs, eight significant proteins were uniquely expressed in the atopic dermatitis group. For instance, triosephosphate isomerase (TPI) in Bifidobacteriaceae in the genus Alloscardovia and demethylmenaquinone methyltransferase (DMM) in Bacteroides were shown to potentially play metabolic functional roles related to disease. PPI network analysis revealed seven reporter proteins showing metabolic alterations between the healthy and disease groups associated with the biosynthesis of ubiquinone and other quinones as well as the energy supply. This study serves as a scaffold for microbial community-wide metabolic functional studies of the infant gut microbiome in relation to allergic disease. PeerJ Inc. 2020-09-25 /pmc/articles/PMC7521340/ /pubmed/33033661 http://dx.doi.org/10.7717/peerj.9988 Text en ©2020 Kingkaw et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Kingkaw, Amornthep
Nakphaichit, Massalin
Suratannon, Narissara
Nitisinprasert, Sunee
Wongoutong, Chantha
Chatchatee, Pantipa
Krobthong, Sucheewin
Charoenlappanit, Sawanya
Roytrakul, Sittiruk
Vongsangnak, Wanwipa
Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
title Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
title_full Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
title_fullStr Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
title_full_unstemmed Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
title_short Analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
title_sort analysis of the infant gut microbiome reveals metabolic functional roles associated with healthy infants and infants with atopic dermatitis using metaproteomics
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521340/
https://www.ncbi.nlm.nih.gov/pubmed/33033661
http://dx.doi.org/10.7717/peerj.9988
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