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A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area

Data from recent studies support the hypothesis that infections by human gastrointestinal (GI) helminths impact, directly and/or indirectly, on the composition of the host gut microbial flora. However, to the best of our knowledge, these studies have been conducted in helminth-endemic areas with mul...

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Autores principales: Jenkins, Timothy P., Formenti, Fabio, Castro, Cecilia, Piubelli, Chiara, Perandin, Francesca, Buonfrate, Dora, Otranto, Domenico, Griffin, Julian L., Krause, Lutz, Bisoffi, Zeno, Cantacessi, Cinzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199319/
https://www.ncbi.nlm.nih.gov/pubmed/30353019
http://dx.doi.org/10.1038/s41598-018-33937-3
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author Jenkins, Timothy P.
Formenti, Fabio
Castro, Cecilia
Piubelli, Chiara
Perandin, Francesca
Buonfrate, Dora
Otranto, Domenico
Griffin, Julian L.
Krause, Lutz
Bisoffi, Zeno
Cantacessi, Cinzia
author_facet Jenkins, Timothy P.
Formenti, Fabio
Castro, Cecilia
Piubelli, Chiara
Perandin, Francesca
Buonfrate, Dora
Otranto, Domenico
Griffin, Julian L.
Krause, Lutz
Bisoffi, Zeno
Cantacessi, Cinzia
author_sort Jenkins, Timothy P.
collection PubMed
description Data from recent studies support the hypothesis that infections by human gastrointestinal (GI) helminths impact, directly and/or indirectly, on the composition of the host gut microbial flora. However, to the best of our knowledge, these studies have been conducted in helminth-endemic areas with multi-helminth infections and/or in volunteers with underlying gut disorders. Therefore, in this study, we explore the impact of natural mono-infections by the human parasite Strongyloides stercoralis on the faecal microbiota and metabolic profiles of a cohort of human volunteers from a non-endemic area of northern Italy (S+), pre- and post-anthelmintic treatment, and compare the findings with data obtained from a cohort of uninfected controls from the same geographical area (S−). Analyses of bacterial 16S rRNA high-throughput sequencing data revealed increased microbial alpha diversity and decreased beta diversity in the faecal microbial profiles of S+ subjects compared to S−. Furthermore, significant differences in the abundance of several bacterial taxa were observed between samples from S+ and S− subjects, and between S+ samples collected pre- and post-anthelmintic treatment. Faecal metabolite analysis detected marked increases in the abundance of selected amino acids in S+ subjects, and of short chain fatty acids in S− subjects. Overall, our work adds valuable knowledge to current understanding of parasite-microbiota associations and will assist future mechanistic studies aimed to unravel the causality of these relationships.
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spelling pubmed-61993192018-10-25 A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area Jenkins, Timothy P. Formenti, Fabio Castro, Cecilia Piubelli, Chiara Perandin, Francesca Buonfrate, Dora Otranto, Domenico Griffin, Julian L. Krause, Lutz Bisoffi, Zeno Cantacessi, Cinzia Sci Rep Article Data from recent studies support the hypothesis that infections by human gastrointestinal (GI) helminths impact, directly and/or indirectly, on the composition of the host gut microbial flora. However, to the best of our knowledge, these studies have been conducted in helminth-endemic areas with multi-helminth infections and/or in volunteers with underlying gut disorders. Therefore, in this study, we explore the impact of natural mono-infections by the human parasite Strongyloides stercoralis on the faecal microbiota and metabolic profiles of a cohort of human volunteers from a non-endemic area of northern Italy (S+), pre- and post-anthelmintic treatment, and compare the findings with data obtained from a cohort of uninfected controls from the same geographical area (S−). Analyses of bacterial 16S rRNA high-throughput sequencing data revealed increased microbial alpha diversity and decreased beta diversity in the faecal microbial profiles of S+ subjects compared to S−. Furthermore, significant differences in the abundance of several bacterial taxa were observed between samples from S+ and S− subjects, and between S+ samples collected pre- and post-anthelmintic treatment. Faecal metabolite analysis detected marked increases in the abundance of selected amino acids in S+ subjects, and of short chain fatty acids in S− subjects. Overall, our work adds valuable knowledge to current understanding of parasite-microbiota associations and will assist future mechanistic studies aimed to unravel the causality of these relationships. Nature Publishing Group UK 2018-10-23 /pmc/articles/PMC6199319/ /pubmed/30353019 http://dx.doi.org/10.1038/s41598-018-33937-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jenkins, Timothy P.
Formenti, Fabio
Castro, Cecilia
Piubelli, Chiara
Perandin, Francesca
Buonfrate, Dora
Otranto, Domenico
Griffin, Julian L.
Krause, Lutz
Bisoffi, Zeno
Cantacessi, Cinzia
A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area
title A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area
title_full A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area
title_fullStr A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area
title_full_unstemmed A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area
title_short A comprehensive analysis of the faecal microbiome and metabolome of Strongyloides stercoralis infected volunteers from a non-endemic area
title_sort comprehensive analysis of the faecal microbiome and metabolome of strongyloides stercoralis infected volunteers from a non-endemic area
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199319/
https://www.ncbi.nlm.nih.gov/pubmed/30353019
http://dx.doi.org/10.1038/s41598-018-33937-3
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