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Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans

Recent studies highlight the importance of intestinal fungal microbiota in the development of human disease. Infants, in particular, are an important population in which to study intestinal microbiomes because microbial community structure and dynamics during this formative window of life have the p...

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Autores principales: Heisel, Timothy, Podgorski, Heather, Staley, Christopher M., Knights, Dan, Sadowsky, Michael J., Gale, Cheryl A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338280/
https://www.ncbi.nlm.nih.gov/pubmed/25706290
http://dx.doi.org/10.1371/journal.pone.0116705
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author Heisel, Timothy
Podgorski, Heather
Staley, Christopher M.
Knights, Dan
Sadowsky, Michael J.
Gale, Cheryl A.
author_facet Heisel, Timothy
Podgorski, Heather
Staley, Christopher M.
Knights, Dan
Sadowsky, Michael J.
Gale, Cheryl A.
author_sort Heisel, Timothy
collection PubMed
description Recent studies highlight the importance of intestinal fungal microbiota in the development of human disease. Infants, in particular, are an important population in which to study intestinal microbiomes because microbial community structure and dynamics during this formative window of life have the potential to influence host immunity and metabolism. When compared to bacteria, much less is known about the early development of human fungal communities, owing partly to their lower abundance and the relative lack of established molecular and taxonomic tools for their study. Herein, we describe the development, validation, and use of complementary amplicon-based genomic strategies to characterize infant fungal communities and provide quantitative information about Candida, an important fungal genus with respect to intestinal colonization and human disease. Fungal communities were characterized from 11 infant fecal samples using primers that target the internal transcribed spacer (ITS) 2 locus, a region that provides taxonomic discrimination of medically relevant fungi. Each sample yielded an average of 27,553 fungal sequences and Candida albicans was the most abundant species identified by sequencing and quantitative PCR (qPCR). Low numbers of Candida krusei and Candida parapsilosis sequences were observed in several samples, but their presence was detected by species-specific qPCR in only one sample, highlighting a challenge inherent in the study of low-abundance organisms. Overall, the sequencing results revealed that infant fecal samples had fungal diversity comparable to that of bacterial communities in similar-aged infants, which correlated with the relative abundance of C. albicans. We conclude that targeted sequencing of fungal ITS2 amplicons in conjunction with qPCR analyses of specific fungi provides an informative picture of fungal community structure in the human intestinal tract. Our data suggests that the infant intestine harbors diverse fungal species and is consistent with prior culture-based analyses showing that the predominant fungus in the infant intestine is C. albicans.
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spelling pubmed-43382802015-03-04 Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans Heisel, Timothy Podgorski, Heather Staley, Christopher M. Knights, Dan Sadowsky, Michael J. Gale, Cheryl A. PLoS One Research Article Recent studies highlight the importance of intestinal fungal microbiota in the development of human disease. Infants, in particular, are an important population in which to study intestinal microbiomes because microbial community structure and dynamics during this formative window of life have the potential to influence host immunity and metabolism. When compared to bacteria, much less is known about the early development of human fungal communities, owing partly to their lower abundance and the relative lack of established molecular and taxonomic tools for their study. Herein, we describe the development, validation, and use of complementary amplicon-based genomic strategies to characterize infant fungal communities and provide quantitative information about Candida, an important fungal genus with respect to intestinal colonization and human disease. Fungal communities were characterized from 11 infant fecal samples using primers that target the internal transcribed spacer (ITS) 2 locus, a region that provides taxonomic discrimination of medically relevant fungi. Each sample yielded an average of 27,553 fungal sequences and Candida albicans was the most abundant species identified by sequencing and quantitative PCR (qPCR). Low numbers of Candida krusei and Candida parapsilosis sequences were observed in several samples, but their presence was detected by species-specific qPCR in only one sample, highlighting a challenge inherent in the study of low-abundance organisms. Overall, the sequencing results revealed that infant fecal samples had fungal diversity comparable to that of bacterial communities in similar-aged infants, which correlated with the relative abundance of C. albicans. We conclude that targeted sequencing of fungal ITS2 amplicons in conjunction with qPCR analyses of specific fungi provides an informative picture of fungal community structure in the human intestinal tract. Our data suggests that the infant intestine harbors diverse fungal species and is consistent with prior culture-based analyses showing that the predominant fungus in the infant intestine is C. albicans. Public Library of Science 2015-02-23 /pmc/articles/PMC4338280/ /pubmed/25706290 http://dx.doi.org/10.1371/journal.pone.0116705 Text en © 2015 Heisel et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Heisel, Timothy
Podgorski, Heather
Staley, Christopher M.
Knights, Dan
Sadowsky, Michael J.
Gale, Cheryl A.
Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans
title Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans
title_full Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans
title_fullStr Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans
title_full_unstemmed Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans
title_short Complementary Amplicon-Based Genomic Approaches for the Study of Fungal Communities in Humans
title_sort complementary amplicon-based genomic approaches for the study of fungal communities in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338280/
https://www.ncbi.nlm.nih.gov/pubmed/25706290
http://dx.doi.org/10.1371/journal.pone.0116705
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